Browse CME Sessions
ѻý Program
A Little Less Conversation, a Little More Action: An Outcome Equity Roadmap for Children and AYAs With Leukemia and Lymphoma
Centuries of structural racism have contributed to discrimination, environmental and social injustice, and household material hardship among historically marginalized populations. Recent studies have highlighted the impact of factors such as income and insurance status on cancer outcomes and health equity. Under-representation of specific groups has limited our understanding of cancer risk, disease biology, treatment-related toxicities, and patient-reported outcomes. The educational objective of this session is to present the latest evidence regarding modifiable factors that contribute to outcome disparities in childhood/adolescent and young adult (AYA) hematologic malignancies, and to discuss potential targets for interventions that address these disparities. Dr. Ji will present an in-depth overview of public health insurance programs in the U.S. and related implications on outcome disparities among AYAs with blood cancers. Using a case-based approach, Dr. Ji will discuss opportunities to improve access to high-quality public health insurance, subsequent to the Affordable Care Act. Dr. Umaretiya will discuss the role of social determinants of health (SDOH) as modifiable drivers of outcome inequities in pediatric oncology. She will review the prevalence of SDOH in pediatric oncology, present historically marginalized parent perspectives on unmet social needs during cancer care, and highlight novel interventions addressing this population’s SDOH and social needs. Dr. Mittal will discuss factors contributing to low rates of enrollment of AYAs with hematologic malignancies to clinical trials, including a lack of availability and accessibility. She will provide an up-to-date review of collaborative initiatives that are addressing some of these barriers to improve AYA access to cancer clinical trials.
Chair:
Maria Monica MonicaGramatges,MD,PhD
Texas Children's Hospital
Houston,
TX
Speakers:
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Emory University School of Medicine
Atlanta,
GA
The Lasting Impact of the ACA: How Medicaid Expansion Reduces Outcome Disparities in AYAs With Leukemia and Lymphoma
Puja J.Umaretiya,MD
Childrens Medical Center Dallas, UT Southwestern
Dallas,
TX
Targeting Hardship: Poverty as a Modifiable Risk Factor in Childhood Leukemia and Lymphoma Treatment
Nupur MittalNupur Mittal
Rush University Medical Center
Chicago,
IL
Sharing is Caring: A Network Collaborative Approach to Identify and Address Barriers in Accessing Clinical Trials in AYAs with Leukemia and Lymphoma
A Shifting Landscape: Treatment of MCL
Mantle Cell Lymphoma is a rare subtype of B-cell non-Hodgkin Lymphoma characterized by disease heterogeneity. The approach to treating patients diagnosed with mantle cell lymphoma has evolved over time with therapeutics including high dose cytarabine containing regimens prior to autologous stem cell consolidation, rituximab maintenance and the oral Bruton’s tyrosine kinase inhibitors for relapsed/refractory disease. It is recognized that not all patients benefit from these approaches. This educational session will explore the evolving treatment landscape in mantle cell lymphoma including identification and treatment of patients with high-risk disease, the role of autologous stem cell transplant consolidation in the era of novel therapies and the current and future incorporation of T-cell engaging therapies in the treatment landscape.
Dr. Kami Maddocks will define high-risk features in Mantle Cell Lymphoma associated with inferior prognosis to standard treatment approaches. Clinical trials incorporating Bruton's tyrosine kinase inhibitors into initial therapy will be discussed. The role of targeted and immunotherapy combinations in a “chemotherapy-free” approach will be presented.
Dr. Martin Dreyling will discuss the role of autologous stem cell transplantation and additional consolidation/maintenance therapies in first line treatment. Clinical trials incorporating Bruton's tyrosine kinase inhibitors into initial therapy will be mentioned. Differential treatment strategies according to clinically applicable biological risk factors will be suggested.
Dr. Lia Palomba will review T-cell engaging therapies in relapsed or refractory Mantle Cell Lymphoma, including CAR T-cells and bispecific antibodies. She will review available data on the outcome of these therapies in the general MCL population and in high-risk subgroups.
Chair:
Kami J.Maddocks,MD
The Ohio State University
Columbus,
OH
Speakers:
Kami J.Maddocks,MD
The Ohio State University
Columbus,
OH
Your Chemo is No Good Here: Management of High-Risk MCL
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LMU University Hosptial München
Munich,
Germany
To Consolidate or Not to Consolidate – The Role of Autologous Stem Cell Transplantation in MCL
Maria LiaPalomba,MD
Memorial Sloan Kettering
New York,
NY
T-cell–based Therapies for Treating Relapsed or Refractory Mantle Cell Lymphoma
Addressing Unmet Needs in T Cell Lymphomas
The rare nature of peripheral and cutaneous T-cell lymphomas, variable clinical course and only recently evolving understanding of their unique biology make the care of patients with these disease particularly difficult. This educational session will delve into current clinical challenges in management of this difficult to treat population and will focus on the more common subtypes of peripheral T-cell lymphoma and cutaneous T-cell lymphomas. The session first will discuss management, incorporation of novel agents and consideration of personalized approaches in relapsed/refractory peripheral T-cell lymphomas and cutaneous T-cell lymphomas. We will also discuss the utility and timing of both autologous and allogeneic transplant in cutaneous and peripheral T-cell lymphoma.
Dr. Mehta-Shah will discuss current clinical challenges in the management of patients with relapsed/refractory T-cell lymphomas. In the evolving landscape of treatment and biologic considerations, we will discuss the use of both standard agents as well as novel targeted agents in the treatment of this patient population. Given that our understanding of these heterogenous diseases continues to improve, we will discuss strategies for subtypes specific or personalized therapy.
Dr. Horwitz will explore and detail the expanding options for treatment of CTCL.
Dr. Dreger will discuss the role of stem cell transplant (auto and allo) on PTCL and CTCL.
Chair:
NehaMehta-Shah,MD, MSCI
Washington University in St. Louis
St Louis,
MO
Speakers:
NehaMehta-Shah,MD, MSCI
Washington University in St. Louis
St Louis,
MO
BV and Beyond: How to Incorporate Novel Agents into PTCL Management
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Memorial Sloan-Kettering Cancer Center
New York,
NY
Expanding Options for Treatment of CTCL
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Heidelberg,
Germany
The Role of Stem Cell Transplant (auto and allo) in PTCL and CTCL
Adult ALL Advancements: Optimizing Cure in 2024
Acute lymphoblastic leukemia (ALL) in adults is an aggressive condition with historically few long-term survivors. Fortunately, the outlook for ALL in adults is improving rapidly as years of scientific research and clinical investigation begins to pay dividends. Improved understanding of the heterogeneity and varied biological behavior of ALL subtypes has led to routine immunophenotypic and genetic characterization of individual ALL cases in the clinic. Profiling of ALL at diagnosis as well as better ability to track measurable residual disease (MRD) after therapy now permits personalized, risk-adapted treatment recommendations in ALL including the rational application of allogeneic stem cell transplantation. In addition, multiple new targeted and immune therapies have been approved by regulatory authorities for Philadelphia chromosome-positive (Ph+) and negative B-ALL. The rapid pace of scientific and therapeutic advancement in ALL is challenging established standards of care for upfront treatment of adults with newly diagnosed ALL. In this session, the impact of scientific and therapeutic advancements in the initial treatment approach for ALL will be reviewed, with a focus on recent evidence generation.
Dr. Marlise Luskin will review data supporting the selection of various approaches to initial treatment of Ph+ ALL in adults. She will discuss data justifying the use of specific BCR-ABL1 kinase inhibitors including dasatinib, nilotinib, and ponatinib. In this session, she will also review evidence defining the role of conventional chemotherapy, allogeneic transplantation, and the bi-specific T-cell engager (BiTE) blinatumomab in first-line post-remissiont treatment of Ph+ ALL in adults of different ages.
Prof. Matthias Stelljes will discuss the role of novel antibody-based and cell-based immunotherapies in the treatment of ALL in adults. Blinatumomab, the antibody-drug conjugate inotuzumab ozogamicin, and CD19-directed CAR-T cells are current standard-of-care options for patients with relapsed or refractory B-cell ALL. The CD20-targeting monoclonal antibody rituximab and blinatumomab are established components of frontline therapy for patients with CD20-positive ALL and patients with persistent MRD, respectively. More recently, blinatumomab and inotuzumabhave shown promising results in the upfront treatment of patients with B-cell ALL. These data form the basis for evaluating and defining new treatment standards, which will be discussed in this educational session.
Dr. Partow Kebriaei will review risk profiling in adult patients with ALL, and specifically how disease risk informs the decision to recommend transplant in first complete remission. Additionally, she will highlight advancements in GVHD prophylaxis that facilitate greater donor availability and decreased toxicity of transplant. Finally, Dr. Kebriaei will review the optimal sequence for transplant within the context of CAR T therapy.
Chair:
Marlise RLuskin,MD, MSCE
Dana-Farber Cancer Institute
Boston,
MA
Speakers:
Marlise RLuskin,MD, MSCE
Dana-Farber Cancer Institute
Boston,
MA
PH+ ALL: New Approaches for Upfront Therapy
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University Hospital Muenster
Muenster,
Germany
Ph- ALL: Impact of Immunotherapy in Upfront Treatment
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MD Anderson Cancer Center
Houston,
TX
Transplant in ALL: Who, When, and How?
Adult CAR-T Outcomes: Beyond the Acronyms (OS, PFS, CRS, ICANS)
CAR T-cell therapy has become a standard treatment option resulting in improved progression-free and overall survival in a variety of relapsed and refractory adult hematologic malignancies. The acute toxicities, particularly CRS and ICANS, and outcomes of CAR T-cell therapy have been extensively described. However, as indications and utilization of this treatment have expanded with increasing reports of long-term survivors, it has become increasingly apparent that there are a number of clinically significant, long-term complications and toxicities that may occur in CAR T-cell recipients. Recognition and understanding of these long-term complications are imperative to patient selection, counseling, and management. This session will review and provide guidelines for monitoring and treatment of long-term complications after CAR T-cell therapy in adult patients.
Measuring disease-related and treatment-driven patient-reported outcomes (PROs) as standard of care in patients undergoing CAR T-cell therapy is both feasible and vital. As has been shown with numerous oncology therapies, the assessment of symptom and functioning PROs is now sufficiently mature to justify their contribution to treatment precision, efficiency, and standardization and national and international collaborations. Nonetheless, collaborative efforts among clinicians, symptom researchers, and electronic health system designers are needed to integrate evidence-based PROs into routine patient care after CAR-T cell therapy. This will help in capturing early toxicity and implement timely interventions with the ultimate goal of improving treatment tolerability related to symptom burden and CAR T-cell clinical outcomes.
Adults receiving chimeric antigen receptor (CAR) T-cell therapy may experience late complications distinct from those in the early CAR T-cell treatment period. Late complications include cytopenias, infections, secondary malignancies, and delayed neurotoxicities. Late cytopenias may be from prolonged recovery after lymphodepleting chemotherapy or arise anew, raising concerns for recurrent disease or a secondary malignancy. Late infections, which are predominantlyviral, may require ongoing prophylaxis and immunoglobulin replacement therapy. Both hematologic and solid secondary malignancies are a known risk of CAR T-cell therapy, with recent observations of T-cell cancers. It is essential to monitor for late complications in adult patients receiving CAR T-cells to improve the outcomes and quality of life.
Infections following CAR-T remain a notable cause of morbidity and mortality not only in the early (<30 days) post-CAR-T but also persist through the prolonged (30-90 days) and late (>90 days) follow-up. The predisposition to infections results from immunosuppression related to underlying disease, prior cytotoxic therapies, lymphodepletion chemotherapy, delayed hematopoietic recovery, B-cell aplasia, and delayed T-cell immune reconstitution. This draft delineates risk factors and epidemiology of infections along the post-CAR-T timeline. Dr. Jain will further discuss our approach to mitigation and management of infections including antibacterial, antiviral, and antifungal prophylaxis, growth factors to expedite count recovery, immunoglobulin replacement therapy, and re-vaccination programs.
Chair:
Michael RBishop,MD
University of Chicago
Chicago,
IL
Speakers:
Xin ShelleyWang,MD, MPH
The University of Texas MD Anderson Cancer Center
Houston,
TX
Patient-Reported Outcomes After CAR T-cell Therapy?in Patients with Hematological Malignancies
Michael RBishop,MD
University of Chicago
Chicago,
IL
Late Complications and Long-term Care of Adult CAR T cell Patients
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Johns Hopkins University School of Medicine
Baltimore,
MD
Mitigating and Managing Infection Risk
ALPS, CVID, and LGL: When Autoimmune Cytopenias Are a Marker of Underlying Immune Disease
Autoimmune cytopenias that are chronic, refractory and multi lineage present a challenge in the clinic. However, recent advances exploring their molecular genetic underpinnings have made them more amenable to rationally targeted therapies and forestall end organ damage in the long run. Dr. V. Koneti Rao will discuss diagnosis and management of ALPS-FAS (Autoimmune Lymphoproliferative Syndrome due to FAS variants) and APDS (Activated PI3Kinase Delta Syndrome due to PIK3CD and PIK3R1 genetic variants) including recently licensed targeted treatment for the latter using a PI3Kinsae inhibitor, leniolisib. Dr.Charlotte Cunnigham Rundles will discuss the impact of genetic disorders presenting as CVID (Common Variable Immune Deficiency) affecting multiple organs due to variants in transcription factors, check point inhibitors, chemokines and cytokines. CVID is one of the most common inborn errors of immunity presenting with infections due to insufficient levels of immune globulins and loss of specific antibodies. However, a significant proportion of these patients develop autoimmune multilineage cytopenias and increased susceptibility to malignancies including lymphoma. These conditions may often be the initial manifestation of the underlying immune defect in a patient who has not had significant infections, and these episodes may recur over time. Treatment of the hematologic complications may require frequent and episodic use of corticosteroids, and/or rituximab; splenectomy is discouraged. Genetic associations noted in CVID patients include CTLA4, LRBA, IKZF1, NFKB1 and NFKB2,STAT3 and STAT1 variants that might provide opportunities for targeted therapeutics. Dr.Thierry Lamy will highlight the impact of clonal evolution of T and Nk cells in LGL (large granular lymphocytosis).Large granular lymphocyte (LGL) leukemia is a rare T/NK cell driven chronic lymphoproliferative disease characterized by neutropenia, anemia and autoimmune disorders such as rheumatoid arthritis, Sjogren syndrome, vasculitis, and autoimmune endocrinopathies. Recent advances in the pathogenesis of LGL leukemia have highlighted the implication of STAT3 genetic variants playing a pivotal role in the leukemic cell proliferation and survival, and autoimmunity. The genetic landscape of LGL is afflicted with gene mutations affecting NF-KB pathway (TNFAIP3), epigenome (TET2, KMT2D), and microenvironment (CCL22). Immunosuppressive agents (cyclophosphamide, methotrexate and cyclosporine) constitute the foundation of first line therapy. Recent advances have led to the development of targeted approaches, including JAK-STAT inhibitors, cytokine targeting and hypomethylating agents, opening novel approaches in an otherwise incurable disease.
Chair:
V. KonetiRao,MD
National Institutes of Health
Bethesda,
MD
Speakers:
V. KonetiRao,MD
NIH
Bethesda,
MD
Beyond FAScinating: Advances in Diagnosis and Management of Autoimmune Lymphoproliferative Syndrome (ALPS)
CharlotteCunningham-Rundles,MD, PhD
Mount Sinai School of Medicine
New York,
NY
Common Variable Immunodeficiency (CVID): Hematologic Presentation and Advances in Molecular Diagnosis
ThierryLamy,MD, PhD
Pontchaillou Hospital Rennes UNIVERSITY HOSPITAL
Rennes,
France
Large Granular Lymphocytosis (LGL): A Clonal Disorder with Autoimmune Manifestations
AML M&Ms: How to Integrate Mutations and MRD Data
The genomic heterogeneity of AML, the clinical variability of patients and patient outcomes to various therapies, and the underlying awareness and evaluation of clonal evolution mandates an integrated approach to AML risk assessment and treatment decision-making. This session will focus on the clinical management of AML using a comprehensive evaluation including both genetic characterization and MRD-based response assessments during therapy, to optimize the clinical outcomes of patients with AML.
Dr. Jerald Radich will examine the role of MRD as an indicator of treatment response, and help answer the question of why some patients with persistent MRD do not relapse, while others without detectable MRD may still relapse nonetheless. He will explore how to best use MRD to optimize patient care, and explore how the mutational landscape of AML at diagnosis and during therapy can help to explain not only the clinical utility of MRD but also key features of leukemia biology.
Dr. Michael Heuser will discuss the prognostic impact of MRD status in different genetic risk groups and provide an overview on the available MRD technologies to monitor treatment response in transplant-eligible patients with AML. He will help to unravel the complex matrix of MRD and mutational dependencies for practical clinical application and management decisions in patients with AML.
Dr. Courtney DiNardo will summarize the current treatment landscape of AML in patients ineligible for transplant, and focus on the importance of a comprehensive genomic assessment to identify optimal treatment strategies both at diagnosis and relapse. She will also highlight the role of MRD assessments and review the role of MRD measurements to guide treatment decisions in patients receiving non-intensive therapies.
Chair:
Courtney D.DiNardo,MD,MSc
MD Anderson Cancer Center
Houston,
TX
Speakers:
Jerald P.Radich,MD
University of Washington School of Medicine
Seattle,
WA
Mutations and MRD: Clinical Implications of Clonal Ontogeny
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Hannover Medical School
Hannover,
Germany
Mutation and MRD-informed Treatment Decisions for the Transplant-Eligible Patient
Courtney D.DiNardo,MD,MSc
MD Anderson Cancer Center
Houston,
TX
Incorporating Mutational Data and MRD Assessments into Treatment Decisions for Transplant-Ineligible Patients
Anticoagulation SOS: Navigating Monitoring Conundrums
Anticoagulation monitoring challenges are encountered commonly in clinical practice. This educational session will present clinically oriented approaches to understanding and managing anticoagulation monitoring challenges associated with direct oral anticoagulant (DOAC) use, heparin monitoring, and anticoagulation for antiphospholipid antibody syndrome.
Dr. Deborah Siegal will review the potential benefits and limitations of DOAC measurement. Clinical situations in which DOAC measurement may be helpful will be discussed and DOAC testing options will be presented based on the goal of measurement.
Dr. Cheryl Maier will review the definition of heparin resistance which varies depending on specific measurements of anticoagulation and the type of assay used. Multiple causes of heparin resistance will be covered using a case-based approach to help providers troubleshoot heparin resistance and develop alternative management strategies when heparin resistance is encountered.
Prof. Hannah Cohen will summarise the use of warfarin in patients with thrombotic antiphospholipid syndrome (APS). Using a case-based approach, she will highlight key considerations in the choice of oral anticoagulant, issues that may impact on accurate monitoring of warfarin anticoagulation in APS patients, and strategies to overcome these. She will also discuss the use and monitoring of low-molecular-weight/unfractionated heparin in APS patients in particular situations.
Chair:
DeborahSiegal,MD, MSc
University of Ottawa
Ottawa,
ON,Canada
Speakers:
DeborahSiegal,MD, MSc
University of Ottawa
Ottawa,
ON,Canada
Measuring the effect of DOACs: Why, When, and How?
Cheryl LMaier,MD, PhD
Emory University
Atlanta,
GA
Troubleshooting Heparin Resistance
HannahCohen,MD, FRCP, FRCPath
University College London Hospitals NHS Foundation Trust
London,
United Kingdom
Warfarin and Heparin Monitoring in Antiphospholipid Syndrome
Beyond TTP: “Atypical” TMAs for the Hematologist
The ѻý educational session will delve into the complexities of thrombotic microangiopathies (TMAs) outside the typical presentation of thrombotic thrombocytopenic purpura (TTP).
The session will address three related disease states: Transplant-Associated Thrombotic Microangiopathy (TA-TMA), atypical Hemolytic Uremic Syndrome (aHUS) and Catastrophic Antiphospholipid Antibody Syndrome (CAPs).
The segment on TA-TMA will cover its incidence in the post-transplant period, the challenges of distinguishing TA-TMA from other post-transplant complications, and the data on emerging treatment approaches. The session will also include a comprehensive review of aHUS, focusing on its genetic underpinnings, atypical presentations, and the latest advancements in targeted therapies, such as complement inhibitors. The discussion will encapsulate the nuances of managing these atypical TMAs, highlighting case studies and clinical trials that underscore the critical role of personalized medicine in improving patient outcomes. This session will also explore Catastrophic Antiphospholipid Syndrome (CAPS), a rare and severe subtype of antiphospholipid syndrome characterized by widespread microvascular thrombi, leading to multiple organ failure. The talk will provide an overview of the pathophysiology, diagnostic criteria, and emerging treatment strategies. Discussion will also focus on distinguishing CAPS from other TMAs through clinical presentation and laboratory findings, emphasizing the importance of timely and accurate diagnosis to mitigate the high mortality rate associated with this condition.
Chair:
MarkCrowther,MS MSc LLM FRCPC FRSC
McMaster University
Hamilton,
ON,Canada
Speakers:
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Washington University in St. Louis
St. Louis,
MO
Atypical HUS: Diagnosis, Management, and Discontinuation Therapy
AngLi,MD, MS
Baylor College of Medicine
Houston,
TX
Transplant Associated TMA: The Conundrum of Diagnosis and Treatment
MarkCrowther,MS MSc LLM FRCPC FRSC
McMaster University
Hamilton,
ON,Canada
Catastrophic Antiphospholipid Syndrome (CAPS) and Anticoagulant-Refractory APS
Challenges and Opportunities of Sickle Cell Care in Africa
This session will discuss the current state of therapies for sickle cell disease in Africa. Access barriers to disease-modifying and curative treatments for sickle cell anemia will be identified, and recommendations of strategies to address some of these barriers will be proposed. The case will be made to prioritize widespread use of hydroxyurea therapy as the bedrock of sickle cell anemia care in Africa.
Chair:
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The Hospital for Sick Children (SickKids) and the University of Toronto
Toronto,
ON,Canada
Speakers:
Obiageli ENnodu,MD
University of Abuja
Abuja,
Nigeria
Newborn Screening Initiatives for Sickle Cell Disease in Africa
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The Hospital for Sick Children (SickKids) and the University of Toronto
Toronto,
ON,Canada
Transfusion, Disease-Modifying Treatments, and Curative Therapies for Sickle Cell Disease in Africa: Where Are We Now?
Kofi A.Anie
London North West University Healthcare NHS Trust and Imperial College London
London,
ENG,United Kingdom
The Intersection of Sickle Cell Disease, Stigma, and Pain in Africa
Challenges in Cancer-Associated Thrombosis
Patients with cancer have an increased risk of venous thromboembolism (VTE) for which anticoagulation is the treatment of choice. However, they also commonly face complications related to cancer itself or cancer therapies that create unique challenges for the management of cancer-associated thrombosis. This educational session will explore the evidence for best practices in assessing and managing challenging scenarios in patients with cancer-associated thrombosis, including patients with brain metastasis, recurrent venous thromboembolism despite anticoagulation, and thrombocytopenia.
Dr. Leader will summarize the evidence of anticoagulant use in patients with brain metastasis, discuss risks and benefits of anticoagulation in these patients and optimal management strategies in this high-risk population.
Dr. Zwicker will discuss the challenges of evaluating and managing patients with cancer and new or progressive VTE on anticoagulation. He will discuss diagnostic strategies to identify etiologies for anticoagulant failure and provide therapeutic options in this patient population.
Dr. Ay will address the challenge of concurrent VTE and thrombocytopenia in patients with cancer. He will summarize data from available literature, review guidance recommendations, and discuss management strategies and future directions in these patients.
Chair:
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Ottawa Hospital Research Institute, University of Ottawa
Ottawa,
ON,Canada
Speakers:
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Memorial Sloan Kettering Cancer Center
New York,
NY
Management of Anticoagulation in Patients With Brain Metastasis
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Memorial Sloan Kettering
NYC,
NY
Trousseau’s Syndrome: Management of Refractory VTE
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Medical University of Vienna
Vienna,
Austria
Treatment of VTE in the Thrombocytopenic Cancer Patient
Chasing Zebras: Navigating Rare Myeloid Neoplasms
It turns out the old adage from our medical school days, “If you hear hoofbeats, think of horses, not zebras,” was not completely correct! Indeed, the diagnosis of a “rare disease” turns out to be not as rare as we previously thought. The faculty speaking in this important session have focused their entire careers to patient care and cutting-edge research in areas of rare and even ultra-rare hematologic malignancies. The coupling of increasing pathologic technology and diagnostic methods along with augmented education and awareness have shed light on some of the more rare blood cancers in our field, especially over the past decade. In particular, in the field of myeloid neoplasms, the emerging importance of dividing these entities into specific subgroups distinguished by unique clinicopathologic characteristics has had a tremendous impact not only on diagnosis, but also on prognosis and development of novel treatment decision approaches.
In this first talk, Dr Robert P Hasserjian focuses his remarks on understanding the growing field of chronic neutrophilic leukemia (CNL) and CSF3R-related disorders. In the decade since the elucidation by, Maxson et al (Maxson, NEJM 2013), of frequent oncogenic CSF3R mutations in patients with CNL and atypical CML, this field has rapidly expanded as we are beginning to understand that these Philadelphia negative hematologic myeloid malignancies are more commonly present than we previously thought.
In the second talk, Dr Naveen Pemmaraju highlights the encouraging developments in a rapidly emerging field in hematologic malignancies, that of Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN). BPDCN is a singularly unique malignancy that is known for involving cutaneous sites, followed by bone marrow/blood lymph nodes, and of interest, a high rate of CNS involvement. Despite many nomenclature and disease category changes over the past three decades, BPDCN is now recognized as its own unique entity which expresses, via flow cytometry and immunohistochemistry: CD123+, along with CD4+, CD56+, TCL-1+ and TCF-4+. The clinical pioneering of the first approved CD123-targeted agent in the field (tagraxofusp, led by Pemmaraju et al NEJM April 2019) has led to the development of a worldwide clinical/translational interest in BPDCN, targeting CD123 by various therapeutic approaches, and for interest in developing combination approaches and CNS-directed therapies for this rare blood cancer.
In the final talk of this session, Dr Olga Weinberg very nicely draws attention to acute leukemias of ambiguous lineage, a field that is rapidly growing as it benefits from deeper, faster, and more directed targeted sequencing efforts and improved patho-biologic understanding of the various subsets that make up this unique entity. Among the keys to this topic will be understanding several of the newer tests, at the level of the blood, bone marrow, flow cytometry, cytogenetics and molecular next generation sequencing that are available in the pathologists’ and clinicians’ tool kits in searching for identification and diagnosis of particular subtypes of this historically elusive diagnosis that is becoming more and more common to encounter.
Chair:
ʱ,Ѷ
MD Anderson Cancer Center
Houston,
TX
Speakers:
Robert PHasserjian,MD
Massachusetts General Hospital
Boston,
MA
The Spectrum of Ph Negative Disease: CNL and CSF3R-Related Disorders
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MD Anderson Cancer Center
Houston,
TX
BPDCN State of the Art
Olga K.Weinberg,MD
UT Southwestern
Dallas,
TX
How to Think About Acute Leukemia of Ambiguous Lineage
Follicular Lymphoma: Playing the Long Game
The prolonged survival for most patients with newly diagnosed follicular lymphoma in 2024 is a triumph of the introduction of rituximab a quarter of a century ago. Our improved understanding of follicular lymphoma biology, the heterogeneity of both disease and patients, and new therapeutic options help us in “choosing wisely” the sequencing of treatment for a given patient. We can now be confident of a median 10 years between first and second treatments along with an age-matched survival for patients in sustained remission after immunochemotherapy. In this session, we map the remaining challenges of identifying the minority of patients with early progression and a poor prognosis, as well as the sequencing of the highly promising T-cell immunotherapies for patients with early or multiply-relapsed disease.
In this talk, Dr. Trotman will provide the survival data to equip clinicians in framing optimistic initial conversations with most patients at diagnosis of advanced stage FL. She outlines the expectations of longevity and a “functional cure” for many. She will address considerations of both patient and FL heterogeneity when discussing initial therapy of high tumor burden disease. She provides the data to assist patients who have achieved complete metabolic remission with prognostication and life planning after initial immunochemotherapy.
In this talk, Dr. Casulo will review the origins of POD24 and its impact on survival outcomes in follicular lymphoma. She will review currently available biomarkers and risk calculators for POD24, providing updates on the pathobiology influencing follicular lymphoma prognosis and implicated in POD24. This talk will also explore the impact of histologic transformation on survival in POD24 and outline future directions for management of POD24 in the current era.
Dr. Bartlett will discuss the activity and safety of anti-CD3xCD20 bispecific antibody T-cell engagers and anti-CD19 autologous chimeric antigen receptor T-cells for relapsed or refractory follicular lymphoma. She will review the pivotal clinical trial data, highlighting depth and durations of responses as well as toxicities including cytokine release syndrome, infections, and neurologic events. She will describe a framework for sequencing these classes of agents, additionally taking into account patient factors and logistical considerations.
Chair:
ܻ徱ٳհdzٳ,鴡
Concord Repatriation General Hospital
Concord,
NSW,Australia
Speakers:
ܻ徱ٳհdzٳ,鴡
Concord Repatriation General Hospital
Concord,
NSW,Australia
Follicular Lymphoma: In Pursuit of a Functional Cure
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James P. Wilmot Cancer Center
Rochester,
NY
The POD24 Challenge: Where Do We Go From Here in Follicular Lymphoma?
Nancy L.Bartlett,MD
Washington University School of Medicine
Saint Louis,
MO
Sequencing Bispecific Antibodies and CAR T-cells for FL
Handling Bad News: How to Best Manage TP53 Myeloid Disease?
Mutations of TP53 are present in 10-15% of cases of de novo acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) and approximately 30% of cases of therapy-related myeloid neoplasms. TP53-mutated myeloid disease is associated with complex cytogenetic abnormalities and poor outcome, with a median survival of only 5-10 months. In this educational session, we will explore the impact of TP53 mutation type and number on outcomes and clinical management. We will review current and emerging treatment approaches for this high-risk subtype of AML/MDS.
Dr. Daniel Link will discuss evidence that TP53 hotspot mutations have dominant negative or gain-of function properties and discuss the potential impact on outcome and clinical management. He will review recent data establishing the importance of determining TP53 mutant allele status (monoallelic versus multi-hit).
Dr. Marina Konopleva will review current non-transplant therapeutic approaches for TP53-mutated myeloid disease and discuss new therapies on the horizon, including chimeric antigen receptor therapies, mutated p53 reactivators, Fc fusion protein and monoclonal antibodies targeting various myeloid antigens.
Dr. Hugo Fernandez will discuss the use of allogenic hematopoietic transplant in the treatment of TP53-mutated myeloid disease, including new approaches to tailor conditioning and use maintenance therapy after transplantation.
Chair:
Daniel CLink,MD
Washington University School of Medicine in St. Louis
Saint Louis,
MO
Speakers:
Daniel CLink,MD
Washington University School of Medicine in St. Louis
Saint Louis,
MO
Are TP53 Mutations All Alike?
ѲԲDzԴDZ𱹲
Albert Einstein College of Medicine
Houston,
TX
Non-transplant Treatment Approaches for High-risk TP53 Myeloid Disease
Hugo FranciscoFernandez,MD
Moffitt Malignant Hematology and Cellular Therapy
Pembroke Pines,
FL
Transplant Options and Outcomes for TP53 Myeloid Disease
Hematologic Challenges at the End-of-Life
Management of hematologic conditions for patients at the end of life is both a challenge and an opportunity to provide evidence-based, compassionate care. Care of seriously ill patients entails specific considerations—including incorporating life expectancy, addressing symptom burden, and navigating hospice—that apply across the spectrum of hematologic diseases. Further, there is a growing, multidisciplinary evidence base to support treatment decision-making that this session will review. First, we will discuss optimization of end-of-life care in transfusion-dependent hematologic malignancies. We will then focus on a strategy for management of anticoagulant medications in those with limited life expectancy. Finally, we will address prognostication and palliative care in sickle cell disease.
Dr. Loh will highlight challenges and barriers in implementing timely end-of-life-care and potential strategies to overcome these barriers for patients with transfusion-dependent hematologic malignancies.
Dr. Park's talk "Anticoagulation at the End of Life: Whether, When, and How to Treat," will focus on state-of-the-art evidence from hematology and palliative care science to inform management of anticoagulant medications in patients with life-limiting illness. Dr. Parks will discuss the complexities of anticoagulation at the end of life, opportunities to enhance our knowledge, and outline an approach to care that is based on patients’ values.
Dr. Johnston will discuss challenges in providing high quality end-of-life care for people with SCD, including disease-related, communication-related, and systemic-related challenges and discuss strategies to overcome these challenges, including use of primary and specialty palliative care.
Chair:
Anna L.Parks,MD
University of Utah Health
Salt Lake City,
UT
Speakers:
Kah Poh (Melissa)Loh,MD
University of Rochester
Rochester,
NY
Challenges in Hospice and End-of-Life Care in the Transfusion-Dependent Patient
Anna L.Parks,MD
University of Utah Health
Salt Lake City,
UT
Anticoagulation at the End of Life: Whether, When, and How to Treat
Emily EJohnston
University of Alabama At Birmingham
Birmingham,
AL
End-of-Life in the Sickle Cell Patient: Life Expectancy and the Role of Palliative Care
Hematologic Management of the Patient with Heavy Menstrual Bleeding
Heavy menstrual bleeding (HBM) has an important impact on the physical, emotional and social well-being, and in adolescents, can be the only clinical sign of an underlying bleeding disorder. Due to several medical, economic and social factors, it remains a significantly underdiagnosed and undertreated condition. Hematologists play an important role in the evaluation and care of patients with anemia from chronic blood loss, and may be the first clinicians to identify HMB as its cause. This education session will describe a clinical multidisciplinary approach to the evaluation and treatment of patients presenting with HMB, with a special focus on adolescents. It will provide an overview of diagnostic and management strategies to broaden the tools available to hematologists caring for these patients in different clinical settings.
Dr. Allison P Wheeler will discuss the various tools available for the quantification of menstrual blood loss, including those that evaluate the effect of HMB on quality of life; followed by a description of non-surgical (hormonal and non-hormonal) treatments of HMB, their efficacy, contraindications and selection of the most appropriate therapy using shared decision-making.
Dr. Juliana Perez Botero will present a focused approach to laboratory testing (screening and confirmatory) for patients presenting with HMB in whom von Willebrand Disease is suspected, with emphasis on the effect of pre-analytical variables and testing methodology on the results and their clinical interpretation.
Dr. Janice Staber will discuss the value of multidisciplinary clinics specializing in the care of adolescents with HMB, including their critical components and different care delivery models, and share important lessons learned during the development and implementation of one of these clinics.
Chair:
JulianaPerez Botero,MD
Versiti
Milwaukee,
WI
Speakers:
Allison PWheeler,MD/MSCI
Washington Center for Bleeding Disorders
Seattle,
WA
Quantifying Menorrhagia and Overview of Non-Surgical Management of Heavy Menstrual Bleeding
JulianaPerez Botero,MD
Versiti
Milwaukee,
WI
Von Willebrand Disease and Heavy Menstrual Bleeding: When and How to Test
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University of Iowa Stead Family Children's Hospital
Iowa City,
IA
Heavy Menstrual Bleeding Clinics for Adolescents
HIT-and-Run: Challenges in Diagnosis and Management of Heparin-Induced Thrombocytopenia
In hospitalized patients, the diagnosis and management of heparin induced thrombocytopenia (HIT) is a recurrent challenge. To this end, this session will 1) provide evidence-based practical guidance in the diagnosis and management of suspected and confirmed HIT; 2) classify anti-platelet factor 4 (PF4) antibody mediated disorders (autoimmune HIT), their relationship to heparin exposure, and the role of rapid PF4 and platelet activation assays in diagnosis; and 3) review alternative management strategies when heparin cessation and non-heparin anticoagulants are insufficient in patients who have refractory HIT, experience acute bleeding, or are planned to undergo cardiac surgery. Emphasizing evidence-based strategies, this session will provide practical approaches and system-level interventions for high-quality care.
Chair:
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Duke University
Durham,
NC
Speakers:
Jori E.May,MD
University of Alabama at Birmingham
Birmingham,
AL
Practical Guide to Diagnosis and Management of “Typical” HIT(T)
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Duke University
Durham,
NC
Alternative Approaches to Management of HIT in Complex Scenarios, including Cardiac Surgery
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University College London
London,
ENG,United Kingdom
Demystifying Autoimmune HIT: What It Is, When to Test, and How to Treat
Integrating New Therapies into the Management of Classical Heme Disorders
This session will provide an overview on the current evidence of different novel therapies for the management of Classical Heme Disorders including ß-Thalassemia, Acute Intermittent Porphyria?(AIP) and anemia in chronic kidney disease (CKD).
Dr. Volker Haasewill outline mechanisms of action and pharmacologic properties of HIF-prolyl hydroxylase inhibitors (HIF-PHIs), a new class of oral anemia drugs approved for the use in patients with chronic kidney disease (CKD). He willdiscuss nondesirableon-target and off-target effects, cardiovascular and other safety concerns, and provide a benefit/risk-based perspective on how this new class of oral drugs might impact current management of anemia in CKD. A clinical case is presented that highlights the clinical complexities and therapeutic challenges in the management of anemia in patients with CKD.
Prof. Taher will highlight persisting unmet needs in patients with non-transfusion-dependent and transfusion-dependent ß-thalassemia. His presentation will overview the current evidence base for luspatercept as a novel disease-modifying agent targeting ineffective erythropoiesis in ß-thalassemia. He will also provide guidance on best-practices for practical application of luspatercept in the real world setting and identify emerging data gaps.
For Dr. Dickey’s presentation, she will review the givosiran clinical trial data and the available clinical literature on givosiran, as well as highlight important unanswered questions.
Chair:
Ali T.Taher,MD, FRCP
American University of Beirut Medical Center
Beirut,
Lebanon
Speakers:
Volker HansHaase
Vanderbilt University
Nashville,
TN
Hypoxia-Inducible Factor (HIF) Activators: ANovel Class of Oral Drugs for the Treatment of Anemia of Chronic Kidney Disease
Ali T.Taher,MD, FRCP
American University of Beirut Medical Center
Beirut,
Lebanon
Luspatercept: A Treatment for Ineffective Erythropoesis in Thalassemia
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Massachusetts General Hospital
Boston,
MA
Givosiran: A Targeted Treatment for Acute Intermittent Porphyria
Ironing Out the Wrinkles: Managing Iron Overload in Different Clinical Scenarios
Iron homeostasis and porphyrin metabolism must be closely coordinated to ensure efficient biosynthesis of heme. Disturbed coordination is exemplified by sideroblastic anemias, which are characterized by insufficient incorporation of iron into the end product of the prophyrin biosynthesis pathway, resulting in anemia and mitochondrial as well as systemic iron overload. Conversely, iron overload from other causes, like hereditary hemochromatosis, can have unfavourable effects on porphyrin synthesis, provoking porphyria cutanea tarda. The intricate interplay between iron and porphyrin metabolism can be disturbed by inherited or acquired causes. Therapeutic options to mitigate the ensuing clinical symptoms are highlighted by the three speakers of this session.
Dr. Domenico Girelli will discuss hereditary hemochromatosis according to the recent clinically oriented classification. While hyperferritinemia is common in practice, hemochromatosis accounts for few cases, typically with increased transferrin saturation. HFE-related hemochromatosis has a low penetrance, influenced by lifestyle and dysmetabolic factors. Most patients are currently identified in the early phases before life-threatening manifestations. Phlebotomy remains the mainstay for achieving iron depletion, with blood donation being an option for maintenance. The management of rare, severe non-HFE forms, requiring a comprehensive approach, will also be presented.
Dr. Norbert Gattermann will outline the pathophysiology of systemic iron overload in MDS as well as mitochondrial iron accumulation in patients with acquired sideroblastic anemias. He will explain how SF3B1 mutations and the subsequent missplicing and deficiency of ABCB7 may lead to impaired heme synthesis and excess mitochondrial iron. The rationale for iron chelation therapy in MDS will be considered, together with some of its practical aspects. Finally, Dr. Gattermann will assess the extent to which luspatercept might contribute to the management of iron overload in patients with MDS.
Dr. Rebecca Leaf will focus on porphyria cutanea tarda (PCT), a disorder of heme biosynthesis that arises due to inhibition of hepatic uroporphyrinogen decarboxylase in the setting of increased liver iron content and oxidative stress. Patients with PCT invariably have siderosis on liver biopsy and up to 20% are homozygous for the HFE C282Y mutation. PCT manifests as blistering cutaneous lesions on sun-exposed areas, skin fragility, and elevated plasma and urine porphyrins. Treatment includes therapeutic phlebotomy to decrease total body iron levels and hydroxychloroquine, which reduces hepatic porphyrin content.
Chair:
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Heinrich Heine University Dusseldorf
Dusseldorf,
Germany
Speakers:
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University of Verona
Verona,
Italy
Diagnosis and Management of Hereditary Hemochromatosis: Lifestyle Modification, Phlebotomy, and Blood Donation
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Heinrich Heine University Dusseldorf
Dusseldorf,
Germany
Management of Iron Overload in Acquired Sideroblastic Anemias and MDS: Role of Chelation and Luspatercept
Mass General Hospital Cancer Center
Boston,
MA
Porphyria Cutanea Tarda: A Unique Iron-Related Disorder
It's a Different World: CLL 2024
The treatment of CLL has significantly advanced over the past decade with the introduction of novel targeted therapies. Inhibitors of Bruton’s tyrosine kinase (BTK) as well as BCL2 have supplanted chemoimmunotherapy in both frontline and relapsed therapy. However, while outcomes have improved in the current era, the disease is not cured, and questions still remain about optimal therapies for frontline and relapsed disease. This education session will focus on unanswered questions in CLL, and how current and upcoming research can answer these questions and continue to move the field forward. Dr Stephan Stilgenbauer will discuss risk stratification in CLL and how genomic features influence treatment choice in the frontline setting. He will discuss the implications of genomic risk on outcomes with currently available therapies. Dr Jennifer Woyach will discuss the evidence surrounding doublets and triplets in the frontline treatment of CLL. She will discuss scenarios in which doublets or triplets might be preferred over other standard options, and current and future trials that will help elucidate the use of these treatment for patients. Dr Arnon Kater will discuss the role of immunotherapies in relapsed/refractory CLL. He will discuss the current evidence surrounding transplant, as well as newer paradigms including cellular therapies and bispecific antibodies.
Chair:
Jennifer A.Woyach,MD
The Ohio State University
Columbus,
OH
Speakers:
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University of Ulm
Ulm,
Germany
Risk-Stratification in Frontline CLL Therapy
Jennifer A.Woyach,MD
The Ohio State University
Columbus,
OH
The Evolving Frontline Management of CLL: Are Triplets Better Than Doublets? How Will We Find Out?
Arnon P.Kater,MD,PhD
Amsterdam UMC
Amsterdam,
Netherlands
Relapsed Refractory CLL: The Role of SCT, Cellular and Non-cellular Immunotherapy
Monoclonal Gammopathies: When the Clone Is More Than a Positive Laboratory Finding
On the spectrum of plasma cell dyscrasias monoclonal gammopathy of undetermined significance (MGUS) represents the most commonly encountered condition in clinical practice. While it is clinically silent, the premalignant MGUS clone has the potential to progress to multiple myeloma or a related B-cell lymphoproliferative malignancy usually associated with high tumor burden. In contrast, monoclonal gammopathy of clinical significance (MGCS) is characterized by a small quiescent B-cell clone but significant symptoms caused by the monoclonal immunoglobulin affecting the skin, kidneys and/or nervous system.
Dr. Michaela Liedtke will present recent updates in the epidemiology of MGUS and prevalence of associated conditions based on population screening studies. Recommendations for a cost-effective diagnostic and follow-up approach will be discussed as well as diagnostic advances including mass spectrometry and revised light chain criteria. We will review updates in MGUS risk stratification related to genetics and other clone & host factors and discuss evidence for the emerging role of lifestyle interventions. The presentation will conclude with a brief overview of MGCS and highlight the clinical features and international collaboration that led to the discovery of TEMPI syndrome.
Dr Frank Bridoux will present the main characteristics of the different types of renal disorders associated with MGUS and introduce the concept of monoclonal gammopathy of renal significance (MGRS). The classification of MGRS-related renal disorders will be presented as well as the diagnostic work-up. The principles of hematologic and renal management of MGRS will be described.
Dr. Maite Cibeira will talk to us about monoclonal gammopathy of neurological significance with the aim of simplifying the hematologist’s diagnostic approach, in close collaboration with the neurologist. She will also discuss the available treatment strategies taking into account the rarity of these diseases, which makes it difficult to conduct clinical trials and explains the lack of standardized treatment options, as well as the relevance of supportive care in the context of an essential multidisciplinary management.
Chair:
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Stanford University Cancer Center
Stanford,
CA
Speakers:
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Stanford University Cancer Center
Stanford,
CA
MGUS Where Do We Stand Today?
FrankBridoux,MD, PhD
CHU Poitiers
Poitiers,
France
Renal Manifestations of MGUS
M TeresaCibeira López,MD, PhD
Hospital Clinic of Barcelona, University of Barcelona, IDIBAPS
Barcelona,
Spain
Neurological Manifestations of MGUS
Moving the Needle in Hodgkin Lymphoma
After decades of small incremental shifts in the management of classic Hodgkin lymphoma (cHL), recent studies have accelerated the pace of change in the treatment of cHL. While brentuximab vedotin (BV) has become a standard part of initial treatment for advanced stage disease, studies using PD-1 blockade in the frontline setting are leading to a re-examination of the role of these novel agents for the treatment of cHL. Meanwhile, the novel agents have led to improved outcomes for patients with relapsed/refractory cHL, leading to questions about the timing and role of stem cell transplantation and whether novel therapies alone can lead to durable remission. Dr. Lynch will address whether recent studies using PD1 blockade in frontline treatment of cHL have established a new standard of care for cHL. Dr. Advani will examine the role of BV in the initial treatment of cHL as well as for relapsed/refractory cHL in light of the recent studies in the frontline and salvage setting. Dr. Perales will discuss the evolving role of stem cell transplantation for cHL, optimal salvage regimens, timing and patient selection.
Chair:
Alex F.Herrera,MD
City of Hope
Duarte,
CA
Speakers:
Ryan C.Lynch,MD
Fred Hutchinson Cancer Research Center
Seattle,
WA
Has PD1 Blockade Changed the Standard of Care for cHL?
Ranjana H.Advani,MD
Stanford University
Stanford,
CA
When Should We Use It? The Role of Brentuximab Vedotin in 2024
Miguel AngelPerales,MD
Memorial Sloan Kettering Cancer Center
New York,
NY
When to Use Stem Cell Transplantation for cHL
MPN Practice Pearls: Profiling, Pegylated IFN and Pregnancy
This MPN session focuses on issues of clinical relevance while emphasizing disease biology. The clinical care of patients with MPN is evolving, with increasing evidence indicating that molecular genetic data is an important component of care, both at diagnosis and during follow up. Approximately three years after the approval of ropeginterferon by the Food and Drug Administration (FDA) for the treatment of Polycythemia Vera (PV), it is timely to review the role of pegylated interferon in the treatment of MPN. Finally, as the obstetric population with MPN increases, understanding how to optimize care for patients with MPN during pregnancy is increasingly relevant. Attendees can expect to learn MPN practice pearls in all three sessions!
Dr. Mead will discuss current approaches to molecular profiling of MPN patients, using illustrative clinical case histories to demonstrate how genetic analysis is already fully integrated into MPN diagnostic classification and prognostic risk stratification. He will discuss how molecular profiling can also be used in MPN to measure response to therapy both in clinical trials and routine clinical practice. Taking a forward look, he will discuss how molecular profiling in MPN might be used in the future to select specific molecularly targeted therapies and the role of additional genetic methodologies beyond mutation analysis.
Dr. Kiladjian will discuss the use of pegylated interferon for the treatment of MPN and review the different types of pegylated interferon currently available. He will review in which MPN subtypes pegylated interferon has the greatest clinical efficacy and discuss both hematological and molecular response. He will review the mechanism of action of pegylated interferon and link this to potential for disease modification and prevention of MPN progression. Finally, he will review the limitations of clinical studies with respect to their ability to measure MPN progression, as well as the need for more comprehensive assessment of molecular response.
Dr. Chi-Joan How will discuss practices around the management of pregnancy in MPN patients. As the obstetric population ages and MPNs are being increasingly diagnosed in younger patients, pregnancy in MPNs will become more frequently encountered. She will discuss current data surrounding pregnancy outcomes in MPNs and current recommendations for the use of anti-platelet agents, anticoagulation, and cytoreduction in the ante- and post-partum period. Using a case-based approach, Dr. How will suggest best practices in areas with limited data.
Chair:
AnnMullally,MD
Stanford University School of Medicine
Stanford,
CA
Speakers:
Adam JMead,PhD, MRCP, FRCPath
University of Oxford
Oxford,
ENG,United Kingdom
Molecular Profiling in MPN: Who Should Have It and Why?
Jean-JacquesKiladjian,MD, PhD
Hopital Saint-Louis
Paris,
France
Pegylated IFN: The Who, Why, and How
Chi-JoanHow,MD
Brigham and Women's Hospital
Boston,
MA
Pregnancy: MPN Management Before, During, and After Pregnancy
Newly Diagnosed Multiple Myeloma: Many Choices and More Questions
The treatment of newly diagnosed myeloma has evolved rapidly with the new therapies and different combinations of these, resulting in deeper and more durable responses. The use of autologous stem cell transplantation has also evolved with this progress, and increasingly the initial treatment is being determined agnostic of the transplant eligibility and or desirability. In the decision making process, two factors play an important role, namely the underlying disease risk and the patient functional status or frailty. In particular, increasing disase risk calls for more intense treatments with the goal of achieving MRD negativity while frailty often limits the intensity of the combinations. Phase 3 trials continue to explore the role of quadruplet regimes in older patient populations with increasing depth of response and durable responses, and the nature of the combinations will evolve in the coming years with new classes of drugs being introduced, especially immunotherapies.
Autologous stem cell transplant has been an integral part of myeloma therapy for the past three decades. Originally envisaged as consolidation following initial treatment of newly diagnosed MM in those eligible to undergo the procedure, its role has evolved over time with investigations exploring various aspects including the types of conditioning regimens, role of post-transplant maintenance as well as tandem autologous stem cell transplantation. While the original phase 3 trials compared ASCT with no ASCT and demonstrated improved overall survival, subsequent trials studied the paradigm of delayed ASCT at the time of first relapse, demonstrating significant improvement in PFS but no OS advantage. As the initial therapies for treatment of myeloma has improved with high rate of deep responses, the role of ACT have continued ot be debated, but have maintained its position in the treatment with most recent trials continuing to show an improvement in PFS compared with no ASCT. Dr. Perrot's talk will focus on how ASCT is positioned in the treatment paradigm of MM.
The overall survival in patients with MM over recent decades. This trend is anticipated to further advance with the emergence of T-cell redirecting therapies, including chimeric antigen receptor T-cell (CAR-T) therapy and T-cell engaging bispecific antibodies. Despite these therapeutic advancements, treatment-related adverse events likely impede quality of life. This underscores the imperative of optimizing supportive care strategies to maximize treatment outcomes. Such optimization is crucial not only for patient well-being but also for treatment adherence to sustain long-term disease control. Dr. Zweegmen will discuss treatment and prevention of bone disease, state of the art thrombosis prophylaxis and supportive care during T-cell redirecting therapies targeting BCMA and GPRC5d, amongst which prevention of infections.
Chair:
ShajiKumar,MD
Mayo Clinic
Rochester,
MN
Speakers:
ShajiKumar,MD
Mayo Clinic
Rochester,
MN
What Is the Ideal Approach – Doublet, Triplet or Quadruplet(s)?
AurorePerrot,MD, PhD
CHU de Toulouse, IUCT-O, Université de Toulouse, UPS, Service d’Hématologie
Toulouse,
France
Transplant in Myeloma: Who, When, and Why?
SonjaZweegman,MD, PhD
Amsterdam University Medical Center, Vrije Universiteit Amsterdam
Amsterdam,
Netherlands
Supportive Care in Myeloma – When Treating the Clone Alone Is Not Enough
Not All Lymphadenopathy is Lymphoma: Lymphoproliferative Diseases of Immune Dysregulation
Immune dysregulation often causes lymphadenopathy that requires clinicopathological correlation for accurate diagnosis. This session will review important causes of lymphadenopathy that fall outside the typical spectrum of malignant lymphoma. Castleman disease, IgG4-Related disease and the relationship between EBV and Post-transplant Lymphoproliferative Disorder will be reviewed. A common theme among these sessions is the importance of combining clinical, laboratory, and pathological “clues” to arrive at the best possible diagnosis and management plan.
Dr. Fajgenbaum will provide an overview on the classification, diagnosis, and management of Castleman disease. Castleman disease is a heterogeneous group of lymphoproliferative disorders, and idiopathic multicentric Castleman disease (iMCD) can be particularly difficult to diagnose and distinguish from other inflammatory causes of lymphadenopathy. Diagnostic criteria for iMCD and the subtypes of iMCD including thrombocytopenia, anasarca, (reticulin) fibrosis, renal dysfunction and organomegaly (iMCD-TAFRO), idiopathic plasmacytic lymphadenopathy (iMCD-IPL) and not otherwise specified (iMCD-NOS) will be reviewed.
Dr. Chen will review IgG4-related disease (IgG4-RD), a disease of immune dysregulation with protean manifestations including autoimmune pancreatitis, sclerosing cholangitis, lacrimal and salivary gland swelling, and tubulointerstitial nephritis. The session will focus on an approach to four key manifestations for Hematologists: Polyclonal hypergammaglobulinemia, IgG4-positive plasma cell enriched lymphadenopathy, eosinophilia, and retroperitoneal fibrosis. Practical tips for differentiating IgG4-RD from key mimickers such as Castleman disease, eosinophilic vasculitis, and histiocyte disorders will be highlighted.
Dr. Rouce will discuss the interplay between Epstein-Barr virus (EBV) and Post-tranplant lymphoproliferative disorder (PTLD). The spectrum of PTLD includes three variations of lymphoproliferation: lymphoid hyperplasia, neoplasia and malignancy. Lymphoid hyperplasia is characterized by polyclonal proliferation and non-destructive lesions whereas lymphoid malignancy features monoclonal proliferation and destructive lesions. EBV is the main driver of PTLD, and management ranges from reduction in immunosuppression to intensive, lymphoma-directed therapy.
Chair:
Luke Y. C.Chen,MD,MEd
Dalhousie University
Halifax,
NS,Canada
Speakers:
David C.Fajgenbaum,MD, MBA, MSc
University of Pennsylvania
Philadelphia,
PA
Identifying Castleman Disease from Non-Clonal Inflammatory Causes of Generalized Lymphadenopathy
Luke Y. C.Chen,MD,MEd
Dalhousie University
Halifax,
NS,Canada
IgG-4 Disease for the Hematologist
RayneRouce,MD
Texas Children's Hospital
Houston,
TX
EBV and Post-transplant Lymphoproliferative Disorder (PTLD): A Complex Relationship
Optimizing Non-Curative Therapies for Sickle Cell Disease
Despite expanding curative options, ineffective disease modifying medication use, acute pain management, and care delivery remain the primary challenges for the vast majority of individuals with sickle cell disease (SCD). This educational session will provide a practical guide for effectively using disease modifying medications, the best practices on delivering multi-modal acute pain management, and examples of successful, real-world adaptive clinical care models. Finally, it will discuss the remaining research questions to answer in these areas to optimize the outcomes of individuals with SCD.
Dr. Creary will discuss the disease modifying medications for SCD. The talk will offer practical guidance on how to overcome common treatment barriers and to use disease modifying medications in a way that balances the unique characteristics of these medications and the patients’ desired outcomes.
Dr. Brandow will discuss alternative methods for acute vaso-occlusive pain management. The talk will review recent research that support using non-opioid and non-pharmacologic interventions and the care delivery processes that have been shown to improve acute SCD pain outcomes
Dr. Bartolucci will discuss updating the existing clinical care models to be more personalized, adaptive, and collaborative, in response to the diverse experiences for those with SCD. The talk will discuss challenges in different income countries and the need for appropriate biomarkers and predictive algorithms.
Chair:
Susan ElizabethCreary,MD,MSc
Ohio State University College of Medicine
Columbus,
OH
Speakers:
Susan ElizabethCreary,MD,MSc
Ohio State University College of Medicine
Columbus,
OH
Practical Guide for Disease-Modifying Management of Children and Adolescents with SCD
Amanda M.Brandow,DO,MS
Medical College of Wisconsin
Milwaukee,
WI
Beyond IV Push: Alternative Methods for Management of Acute Pain in SCD
PabloBartolucci
APHP UPEC IMRB
Créteil,
France
Novel Clinical Care Models for Patients with Sickle Cell Disease
Overcoming Post-transplant Relapse: How to Win the Battle Royale
Over the last few decades, significant progress in reducing infectious and immune-related complications of allogeneichematopoietic cell transplantation have improved the feasibility and overall outcome of this complex procedure. Still, in patients patients transplanted for malignant diseases, reappearance of the original cancer, or relapse, continue to represent a crucial clinical issue. This educational session will present current knowledge on the biology of relapse, on how to tailor the transplant protocol to reduce its incidence, and on the use of novel drugs to prevent or treat recurrence.
Dr. Luca Vago will outline available evidence on the dynamic changes occurring in cancer cells and the patient immune system upon allogeneic hematopoietic cell transplantation, with a particular focus on how key aspects of the transplant such as donor choice and use of specific drugs impact on disease evolution, and on how state-of-the-art profiling of relapsed disease can help selecting appropriate countermeasures.
Dr. Ito's session begins by highlighting the current evidence of maintenance therapy for post-transplant relapse prevention, including targeted therapies, hypomethylating agents, venetoclax, and immunotherapies. The talk then shifts the focus to the role of relapse monitoring, emphasizing the importance of measurable residual disease and donor chimerism. Finally, the session will review the salvage therapies for overt relapse, including donor lymphocyte infusion, second allogeneic stem cell transplantation, and selected agents under investigation.
Dr. Pierini will speak on novel conditioning and prophylaxis regimens for relapse prevention.
Chair:
LucaVago,MD,PhD
IRCCS Ospedale San Raffaele
Milano,
Italy
Speakers:
LucaVago,MD,PhD
IRCCS Ospedale San Raffaele
Milano,
Italy
Biology of Transplant Relapse: Actionable Features
AntonioPierini,MD,PhD
University of Perugia
Perugia,
Italy
Novel Conditioning and Prophylaxis Regimens for Relapse Prevention
SawaIto,MD,PhD
University of Pittsburgh
Pittsburgh,
PA
Post-transplant Strategies for Relapse Prevention and Treatment
Sex Hormones, Contraceptives, and Thrombotic Risk: Where Are We Now?
Venous thromboembolism is a common disease, with an incidence of one to three per 1000 individuals per year. Numerous risk factors are known, which can be divided into genetic and acquired. One of the most well-known acquired risk factors is exposure to endogenous (i.e. pregnancy) and exogenous female hormones, including oral contraceptive use, hormone substitution therapy, and gender-affirming hormone therapy. Thrombosis specialists are frequently consulted about optimal hormonal therapy in individuals with an increased risk of venous thromboembolism, as well as optimal management of pregnancy-related venous thromboembolism.
Dr Leslie Skeith will cover contraceptive-related VTE risk by agent and by clinical scenario, including in patients with inherited thrombophilia, systemic lupus erythematosus with or without antiphospholipid antibodies or antiphospholipid syndrome, and sickle cell disease considering contraception. Relevant clinical practice guidelines are reviewed. A multidisciplinary approach to counselling is needed for patient-focused decision-making.
Dr Joseph Shatzel will explore the hematologic complications of gender-affirming therapy, with a particular focus on managing and mitigating the thrombotic risks linked to exogenous estrogen use. He will detail existing data on thrombotic risks reported in transgender individuals and provide insights from studies involving cisgender women and men who receive exogenous estrogen and testosterone, providing important contextual background. He will delve into strategies for addressing testosterone-induced erythrocytosis and iron deficiency in transgender individuals undergoing hormone therapy.
Dr Saskia Middeldorp will present clinical cases of VTE related to hormonal contraceptive use and pregnancy to illustrate key considerations for clinical practice. Practice points for primary VTE treatment and the evidence on the risk of recurrent VTE and bleeding in this population are detailed. The potential value of thrombophilia testing is described including the: “who, why, when, what and how”. We also discuss key aspects of shared decision making for anticoagulant duration, including a reduced dose anticoagulant strategy in hormone-related VTE.
Chair:
SaskiaMiddeldorp,MD, PhD
Radboud university medical center
Nijmegen,
Netherlands
Speakers:
LeslieSkeith
University of Calgary
Calgary,
AB,Canada
Estrogen, Progestin, and Beyond: Thrombotic Risk and Contraceptive Choices
Joseph J.Shatzel,MD
Oregon Health and Science University
Portland,
OR
Gender-Affirming Hormone Therapy in the Transgender Patient: Influence on Thrombotic Risk
SaskiaMiddeldorp,MD, PhD
Radboud university medical center
Nijmegen,
Netherlands
Hormone-Related Thrombosis: Duration of Anticoagulation, Risk of Recurrence, and the Role of Hypercoagulability Testing
The Expanding Landscape of Treatment for ITP
The management of Immune Thrombocytopenia (ITP) has seen a renaissance in the available therapies and in the approach to patients with the diagnosis in recent years. This has lead to an expanding number of therapeutic options for patients and physicians to consider as they embark on their therapeutic journey with ITP. Dr. Waleed Ghanima will discuss the new approaches incorporating combination strategies in management of patients with ITP including suggestions for when to consider moving beyond mono therapy for ITP. Dr. Annemarie Fogerty will then discuss updates on ITP in pregnancy, a special category of ITP with implications for both maternal and fetal health and provide the most information on both treatments and outcomes. Finally, Dr. Michele Lambert will then describe current clinical trials (or recently completed) and provide information on novel therapeutics that are in development as well as the current treatment gaps where additional study is needed.
Chair:
Michele P.Lambert,MD
Children's Hospital of Philadelphia
Philadelphia,
PA
Speakers:
WaleedGhanima,MD,PhD
Østfold Hospital
Gralum,
Norway
Insights on Treatment of ITP: Algorithm for Management and Role of Multi-Modal Therapy
Annemarie EFogerty,M.D.
Massachusetts General Hospital
Boston,
MA
Management of ITP during Pregnancy
Michele P.Lambert,MD
Children's Hospital of Philadelphia
Philadelphia,
PA
On the Horizon: Upcoming New Agents for the Management of ITP
Vascular Anomalies, Vascular Malformations, and the Role of the Hematologist
Vascular anomalies have traditionally been managed by surgical and interventional radiology colleagues. However, an evolving understanding of the pathophysiology, genetic landscape and hematologic outcomes will necessitate involvement from hematologists and oncologists for comprehensive care. This session will explore the molecular underpinnings and genetic factors of these conditions, highlighting the shift towards targeted medical therapies informed by recent discoveries in crucial signaling pathways. The talks will also cover the management of hemostasis and thrombosis risks, stressing the need for a multidisciplinary approach to diagnostics and treatment to enhance patient safety and outcomes. Together, these talks will shed light on the latest scientific advancements and their translation into clinical practices highlighting the pivotal role hematologists and oncologists play in this specialized care.
Dr. Vikkula will present an overview of the current understanding of the pathophysiological foundations of vascular anomalies. He will examine how genetic associations across various clinical cases inform the diagnostic work-up and classification of these conditions. Additionally, he will discuss the pathophysiological effects of the characterized pathogenic variants, which underlie the basis of developing targeted medical therapies for vascular anomalies.
Dr. Borst’s talk will review currently available medical therapies for vascular anomalies, review guidelines for drug dosing and monitoring, and introduce some novel therapeutics. The discovery of somatic pathogenic variants in thePI3K/AKT/mTOR and Ras/MAPKintracellular signaling pathways as drivers of vascular anomalies has led to a new era of precision medicine for these malformations and tumors. Hematologists/oncologists are critical to the care of patients with vascular anomalies, owing to expertise in managing targeted medical therapies.
Dr. Crary’s talk will focus on the evolving role of hematologists in diagnosing and managing consumptive coagulopathy associated with vascular anomalies such as kaposiform hemangioendothelioma and slow-flow vascular malformations She will emphasize the importance of interdisciplinary approaches, especially in peri-operative settings, to prevent complications like bleeding and venous thromboembolism. The talk illustrates the use of clinical signs, imaging, laboratory findings, and anticoagulation therapy to improve patient outcomes.
Chair:
Shelley ECrary,MD, MS
Arkansas Children's Hospital
Little Rock,
AR
Speakers:
MiikkaVikkula,MD, PhD
Universite Catholique De Louvain
Brussels,
Belgium
Molecular Landscape and Classification of Vascular Anomalies
Alexandra JaneBorst,MD
The Children's Hospital of Philadelphia
Philadelphia,
PA
Targeted Medical Therapies for Vascular Anomalies
Shelley ECrary,MD, MS
Arkansas Children's Hospital
Little Rock,
AR
Hemostasis and Thrombosis Risks and Management in Vascular Anomalies
ѻý Spotlight Sessions
Curative Therapies for Sickle Cell Disease: Option for Some but Not Quite All
Despite substantial improvements in care, individuals with sickle cell disease continue to experience substantial morbidity and a shortened life expectancy.With recent advances in the development of curative therapies, including allogeneic stem cell transplantation and gene therapy, it is important to identify barriers to accessing these treatments and adequately define suitable candidates for curative therapies.
In this session, Dr. Santosh Saraf will review the current guidelines for curative therapies, discuss the potential benefits and risks of the different curative therapies, and provide insight on when to refer patients for curative therapy.
In the second presentation, Dr. Payal Desai will discuss the various barriers to accessing curative therapies as well as the need for development of an integrated care approach.
Chair:
Kenneth I.Ataga,MD
University of Tennessee Health Science Center
Memphis,
TN
Speakers:
Santosh L.Saraf,MD
University of Illinois Chicago
Chicago,
IL
Curative Therapies in Sickle Cell Disease: Which Patient, What Modality, and When to Refer
PayalDesai,MD
Wake Forest University
Charlotte,
NC
Systemic Barriers to Curative Therapy and Need for Integrated Care
Gene Therapy and Hemophilia A: What Is the Future of Curative Therapy in the Age of Emicizumab?
There have been marked advancements in the treatment of hemophilia A over the past decades. Adoption of routine prophylaxis to prevent bleeding as the standard of care has led to many children growing into adulthood with normal joint function and adults with improved function and quality of life. However, there remains a continued treatment burden and bleeding events, including spontaneous hemorrhage. Newer therapeutics with regulatory approval and in late phase clinical trial may further decrease the treatment burden and improve efficacy. This session will provide an update on gene therapy for hemophilia and discuss gene therapy in the context of new and coming therapies.
Frank W.G. Leebeek, MD, PhD
The Promise of Gene Therapy for Severe Hemophilia A
In the past decade enormous improvements have been made in delivering AAV-based gene therapy in patients with hemophilia A. In several phase 1 and 3 studies patients reached normal levels of FVIII after a single dose of AAV-delivered FVIII-gene construct, leading to reduced bleeding rates and patients could stop regular FVIII prophylaxis. During follow up of more than five years FVIII activity declined over time, however the majority of patients still have residual FVIII expression enabling them to refrain for prophylaxis. These promising results led to FDA and EMA approval of gene therapy for hemophilia A in 2022. Longer term follow-up is needed to show us the duration of benefits and (potential) drawbacks of gene therapy compared to current and other novel treatments.
Christine L Kempton, MD, MSc
Unknowns of Gene Therapy and Successes of Medical Therapies for Hemophilia A
Although gene therapy has held the promise of a cure, a consistent cure has yet to be realized. Additionally, the beneficial results seen in hemophilia A gene therapy clinical trials have occurred with meaningful challenges. This talk will review the risks and benefits of gene therapy for hemophilia A and consider them within the context of therapies (emicizumab and Fc-VWF-XTEN fusion protein-eht) that have shown consistent benefit compared with previously available factor VIII products as well as other promising therapies (Mim8, fitusiran, concizumab, and marstacimab) in late-stage clinical trials.
Chair:
Barbara A.Konkle,MD
Bloodworks Northwest
Seattle,
WA
Speakers:
Frank W.G. W.G.Leebeek,MD, PhD
Erasmus university Medical Center
Rotterdam,
Netherlands
The Promise of Gene Therapy for Severe Hemophilia A
Christine LKempton,MD,MSc
Emory University
Atlanta,
GA
Unknowns of Gene Therapy and Successes of Medical Therapies for Hemophilia A
Making a Match: Optimal Donor HLA and Beyond
Selection of the optimal donor for allogeneic hematopoietic cell transplantation (allo-HCT) involves a comprehensive evaluation of several critical factors. Human leukocyte antigen (HLA) matching has proved to be the most likely crucial parameter in this process. However, several additional criteria can significantly influence allo-HCT outcomes.
Dr. Heather Stefanski will discuss the patient’s likelihood and probability of having a fully HLA-matched donor and finding a suitable donor prior to allo-HCT. She will summarize the historical barriers to transplant, especially for racially and ethnically diverse patients. A special focus will be put on new strategies, including post-transplant cyclophosphamide and abatacept, which can allow for safe and effective use of HLA-mismatched donor sources such as haploidentical donors and mismatched unrelated donors. Dr. Stefanski will highlight the research evidence that shows alternative donors are a viable and safe option for many allo-HCT recipients.
Dr. Mohamad Mohty will discuss the non-HLA factors which can contribute to further optimizing the selection of a donor prior to allo-HCT. These factors include the age of the donor (especially data favoring younger donors), recipient-donor gender mismatch and its impact on graft-versus-host disease, cytomegalovirus serostatus, and blood type compatibility. Dr Mohty will also briefly discuss the potential role of killer immunoglobulin-like receptor (KIR) matching, and donor-recipient kinship.
By integrating HLA and non-HLA variables into the donor selection process, one can significantly enhance the outcome of patients who are candidates for allo-HCT.
Chair:
MohamadMohty,MD,PhD
Saint-Antoine Hospital
Paris,
France
Speakers:
Heather E.Stefanski,MD,PhD
CIBMTR® (Center for International Blood and Marrow Transplant Research), NMDP
Minneapolis,
MN
HLA: Optimizing the ’Full HLA Match’
MohamadMohty,MD,PhD
Saint-Antoine Hospital
Paris,
France
Beyond HLA: Optimizing Non-HLA Variables
Smoldering Myeloma: A Case for Early Intervention?
Smoldering Multiple Myeloma (SMM) is a precursor plasma cell disorder characterized by the presence of an M-component concentration equal to or greater than 3 g/dL and/or bone marrow plasma cell infiltration of 10-59%, without any myeloma-defining events. The outcome is heterogeneous, especially regarding progression to active disease such as Multiple Myeloma or other plasma-cell related disorders. The current standard of care is observation, but ongoing and completed research suggests it is possible and straightforward to identify SMM patients at high risk of progression to Multiple Myeloma (50% at 2 years).
This session will feature two clinical cases that highlight the issues involved in determining whether early treatment is the optimal approach for managing this precursor plasma cell disorder and if early treatment is the only way to potentially cure Multiple Myeloma.
Dr. Mateos will discuss the role of early treatment in Smoldering Myeloma as a strategy to cure the disease. She will present evidence supporting the benefits of early intervention and its impact on long-term outcomes.
Dr. Ramasamy will provide a counterpoint to this approach, addressing the costs and toxicities associated with early treatment. He will discuss the potential downsides and argue for a more conservative management approach based on observation.
We look forward to a dynamic and educational session that will provide valuable insights into the management of Smoldering Multiple Myeloma
Chair:
Maria-VictoriaMateos,MD, PhD
University Hospital of Salamanca/IBSAL/Cancer Research Center-IBMCC (USAL-CSIC)
Salamanca,
Spain
Speakers:
Maria-VictoriaMateos,MD, PhD
University Hospital of Salamanca
Salamanca,
Spain
Point: Yes, That is the Only Way We Can Cure Myeloma?
KarthikRamasamy,MD,PhD
University of Oxford
Oxford,
United Kingdom
Counterpoint: No, It Just Adds Cost and Toxicity?
The Clone Wars: Myeloid Neoplasia Risk in Clonal Hematopoiesis
Clonal expansions in the hematopoietic system, referred to as clonal hematopoiesis (CH), is common throughout life and associated with significant clinical outcomes, including increased risk of hematologic cancers, all-cause mortality and nonmalignant conditions. Recently, clinical definitions of disorders within the spectrum of CH have been introduced, including clonal hematopoiesis of indeterminate potential (CHIP) and clonal cytopenia of undetermined significance (CCUS), providing the framework for harmonized classification and registration. However, while clone features and dynamics have been well described, relevant key issues remain to be clarified.
In the first presentation, Dr. Malcovati will provide an overview of biological underpinnings and clinical implications of CH. In addition, the spectrum of clonal cytopenias, as well as current classification framework and its pitfalls, will be critically discussed. Finally, the contribution of intra- and extra-clonal factors to clonal evolution, and the models developed for predicting the risk of developing myeloid neoplasms and the trajectory of evolution will be reviewed, as a basis for informing early-detection and prevention strategies.
In the second presentation, Dr Grønbæk will discuss the clinical management of CH in everyday clinical practice, focusing on how individual/patients with CH are identified, including the incidental finding, which emphasizes the need for informed consent before sequencing. She will elaborate on the importance of identifying and following high-risk individuals/patients while sparing low risk individuals unnecessary worries. The importance of enrolling these individuals/patients in clinical trials will be discussed including the optimal trials designs. Examples of ongoing trials will be presented and critically appraised.
Chair:
LucaMalcovati,MD
University of Pavia and S. Matteo Hospital
Pavia,
Italy
Speakers:
LucaMalcovati,MD
University of Pavia
Pavia,
Italy
Predicting Risk of MN in CH
KirstenGronbaek,Professor, MD, DMSc
Kirsten Grønbæk
Copenhagen N,
Denmark
How to Follow CH Patients
How I Treat
A Personal Journey with Castleman Disease (ticketed session for in-person participants)
Acute Lymphoblastic Leukemia Incorporating New Treatment Options (ticketed session for in-person participants)
Acute Myeloid Leukemia with Targetable Mutations (ticketed session for in-person participants)
Adult Outpatient CAR T Therapy (ticketed session for in-person participants)
Challenges and Management of Cancer Associated Thrombosis (ticketed session for in-person participants)
Follicular Lymphoma Incorporating New Treatment Options (ticketed session for in-person participants)
Gene Therapy in Sickle Cell Disease (ticketed session for in-person participants)
Newly Diagnosed Multiple Myeloma (ticketed session for in-person participants)
Options for Long-Term Management of Hemophilia (ticketed session for in-person participants)
Sickle Cell Disease in Africa (ticketed session for in-person participants)
Marquee Sessions
2024 Ham-Wasserman Lecture
Sickle cell disease (SCD) is an inherited red blood cell (RBC) disorder caused by either homozygous inheritance of the hemoglobin S mutation (HbSS), or compound heterozygous inheritance of the hemoglobin S mutation with another ß-globin chain abnormality. India has among the highest hemoglobin S allele frequencies in the world and the third-highest birth rate for babies born with HbSS.
The Indian sickle cell haplotype is associated with the Arab-Indian or Asian haplotype and is associated with high fetal hemoglobin (HbF) levels and hence, is believed to have mild clinical presentation as compared to other populations.
In this lecture Dr. Dipty Jain will discuss the status of frequency, comorbidities, and management of sickle cell disease (SCD) in India, which is characterized by relatively high percentages of fetal hemoglobin, accompanied by mild to severe complications observed globally. Additionally she will talk about targeted newborn screening and fixed low dose of hydroxyurea in managing children with sickle cell disease in India.
Dr. Jain will discuss the milestones and progress in understanding sickle cell disease (SCD) phenotype accelerated by the Government of India’s ambitious ‘’National Sickle Cell Anemia Elimination Mission 2023’’ with comprehensive guidelines and implementation of screening, treat, counsel, educate, development of technology and novel therapies including gene therapy specific to the requirement of India’s population with sickle cell disease (SCD).
Chair:
MohandasNarla,DSc
New York Blood Center
New York,
NY
Speaker:
Dipty LalitJain
Indira Gandhi Government Medical College and Hospital
NAGPUR,
India
Sickle Cell Disease in Developing Countries
2024 Presidential Symposium
Red cells constitute ~70% of all cells in the human body and in healthy individuals their circulatory life span is ~ 120 days. At steady state the bone marrow produces 2.5 million red cells per second to maintain normal hemoglobin levels. Anemia characterized by decreased hemoglobin levels is a major global health problem affecting nearly 2 billion individuals. Decreased red cell life span and/or decreased red cell production in the bone marrow account for anemia in various inherited and acquired hemolytic anemias. Significant progress has been and is continuing to be made in our understanding of the mechanistic basis for anemia. The three presentations in the symposium will highlight recent advances in our understanding of red cell biology and of anemia.
Dr. Patrick Gallagher will discuss recent advances which have expanded understanding of the many roles of the erythrocyte membrane. An update on the diagnosis and treatment of membrane disorders and potential emerging therapies will be discussed.
Dr. Naomi Taylor will highlight the pivotal role of metabolite transporters and fuel choice in erythroid lineage commitment and terminal erythroid differentiation. The importance of metabolic reprogramming in diseases of disordered and ineffective erythropoiesis will be discussed.
Dr. Olivier Hermine will explain the mechanisms that control red cell production during terminal erythroid differentiation, focusing on the processes that determine the fate of erythroid precursors between differentiation or cell death. The discussion will also touch upon how these mechanisms are impacted in hemoglobinopathies and myelodysplastic disorders, which can result in ineffective erythropoiesis and anemia. Additionally, therapeutic implications arising from these insights will be emphasized.
Chair:
MohandasNarla,DSc
New York Blood Center
New York,
NY
Speakers:
Patrick GGallagher,MD
Abigail Wexner Research Institute at Nationwide Children's Hospital
Columbus,
OH
Mature Red Cell Membrane Disorders (including genome-wide screening and PK activators)
NaomiTaylor,MD
National Institutes of Health
Bethesda,
MD
Metabolism and Erythropoiesis (including metabolism, IDH mutations and relevance to MDS, sideroblastic anemia)
OlivierHermine,MD,PhD
IMAGINE institute Paris France
Paris,
France
Ineffective Erythropoiesis in Thalassemia and Sickle Cell Disease
Meet the Scientist
CAR-T and CAR-NK in Therapy of Hematologic Malignancies
Epigenetic Regulation in Bone Marrow Failure
Mechanisms of Drug Resistance in Acute Myeloid Leukemia
Microenvironment Regulation of Hematopoietic Stem Cells
Pluripotent Stem Cell-Based Modeling of Hematologic Malignancies
Production of Functional Hematopoietic Stem Cells from Pluripotent Cells
Therapy-Related Myeloid Neoplasms
Transferrin Receptor Physiology and Iron Metabolism
What Does the Future Hold for Management of Hemophilia?
Scientific Program
Crosstalk Between Iron Homeostasis and Metabolism
Scientific Committee on Iron and Heme
Maintaining iron balance is fundamental to preserve metabolic functions and energy requirements. This session reflects the current understanding of the reciprocal relationship existing between iron homeostasis and energetic metabolism. It aims to highlight the regulatory role of heme and iron on glucose and lipid metabolism as well as the impact of metabolism on the modulation of the iron status. Novel findings will be presented about the physiologic and pathologic implications of iron-mediated regulation of metabolism, and metabolite-driven control of iron and heme homeostasis. The session will focus on b-thalassemia, sickle cell disease and obesity, and will have broad relevance to all hematologic and non-hematological diseases.
Dr. Antonella Nai will discuss the role of Transferrin Receptor2 (TFR2) in the reciprocal regulation between iron homeostasis, erythropoiesis, and glucose metabolism. TFR2 is an iron sensor acting as a brake of erythropoietin signaling in erythroid cells. Its genetic inactivation in the hematopoietic compartment enhances erythropoiesis and improves anemia in ß-thalassemia. She will present unpublished data demonstrating that Tfr2 deficiency increases the metabolic activity of erythroid cells, thus promoting glucose consumption and reducing blood glycemia. This is particularly relevant in ß-thalassemia, whereby glucose intolerance and diabetes are common and invalidating complications.
Dr. Wei Ying will focus on the connection between iron homeostasis and lipid metabolism. He will present findings related to the role of iron homeostasis in regulating hepatocyte lipogenesis and neighboring cell responses, including hepatic stellate cells, and describe how alterations of these mechanisms drive non-alcoholic fatty liver disease, steatohepatitis and obesity.
Dr. Leitinger will share how heme triggers a unique bioenergetic switch in macrophages, characterized by a metabolic shift from oxidative phosphorylation towards glucose consumption, and its critical role in the effective clearance and detoxification of heme in sickle cell disease. Based on the previous identification of the phosphofructokinase PFKFB3 as key mediator of the metabolic switching in heme-detoxifying macrophages, he will present data about a potential therapeutic strategy involving the inhibition of PFKFB3 in a mouse model of sickle cell disease. Furthermore, the general clinical relevance of these processes for patients with hemolytic disorders will be discussed.
Chair:
FrancescaVinchi,PhD
New York Blood Center
New York,
NY
Speakers:
AntonellaNai,PhD
IRCCS San Raffaele Scientific Institute
Milan,
Italy
Iron, Erythropoiesis, and Glucose Metabolism
WeiYing,PhD
University of California San Diego
La Jolla,
CA
Iron and Lipid Metabolism
NorbertLeitinger
University of Virginia
Charlottesville,
VA
Heme and Macrophage Metabolism.
Host Factors Driving Anti-Leukemia Immunotherapy Outcomes
Scientific Committee on Immunology and Host Defense
This session will cover how the immune microenvironment of the host interacts with leukemia cells and how the donor immune system can exert graft-versus-leukemia (GVL) effects. The speakers will focus on the characterization of immune effector cells and leukemia cells using high resolution RNA and protein analysis, the characterization of metabolites that impact the GVL effect and kinase inhibition strategies to overcome immune escape mechanisms of leukemia cells.
Dr. Catherine Wu will discuss the components critical to devising effective immunotherapy for the treatment of myeloid leukemia, namely the identification of myeloid malignancy antigen targets, and the detection of critical immune cell effectors. The analysis of GvL responses following allogeneic stem cell transplant for AML/MDS, through single cell transcriptome and spatial analysis of marrow specimens, is a particularly instructive setting from which to detect key antigens and cell subpopulations implicated in anti-leukemia responses. The insights gained from the study of such GVL settings promise to provide a roadmap for devising new immunotherapeutic approaches for myeloid malignancies.
Dr. Takanori Teshima will discuss mechanisms of leukemia relapse after allogeneic hematopoietic stem cell transplantation and novel strategies to prevent relapse by inhibiting immune escape of leukemic cells, restoring immune cell dysfunction, and turning “COLD” into “HOT” immune microenvironment. In addition, novel strategies to separate GVL from GVHD by controlling migration and activation of donor T cells in the vicinity of leukemic cells.
Chair:
RobertZeiser,MD
ԾäٲԾܳ Freiburg
Freiburg,
Germany
Speakers:
Catherine J.Wu,MD
Harvard Medical School
Boston,
MA
Immune Microenvironment and GVL Effects
TakanoriTeshima,MD,PhD
Hokkaido University
Sapporo,
Hokkaido,Japan
Firing Up COLD Tumor Microenvironment to Facilitate GVL
FranziskaBlaeschke,MD,PhD
German Cancer Research Center (DKFZ)
Heidelberg,
Germany
Immune Metabolism in T Cells Acting Against Leukemia Cells
Ineffective Erythropoiesis: Insights Into Molecular Mechanisms and Disease Pathophysiology
Scientific Committee on Red Cell Biology
Ineffective erythropoiesis is the leading cause of red cell-related diseases, including anemia, which stands as the most prevalent hematologic disease, affecting millions of individuals worldwide. Understanding the underlying mechanisms of ineffective erythropoiesis is pivotal for advancing diagnostic and therapeutic approaches in hereditary anemias and adult-onset conditions. This session will explore recent breakthroughs in research related to ineffective erythropoiesis, focusing on areas of hemoglobinopathies, malaria infection, and myeloid neoplasms. By bringing together experts at the forefront of these investigations, the session will not only enhance understanding of the pathogenesis of ineffective erythropoiesis but also catalyze the development of innovative approaches to treat related diseases.
Chair:
PengJi,MD,PhD
Northwestern University Medical School
Chicago,
IL
Speakers:
WassimEl Nemer,PhD
French Blood Establishment (EFS)
Marseille,
France
Post-Transcriptional and Signaling Mechanisms in Ineffective Erythropoiesis in Hemoglobinopathies
Elizabeth S.Egan,MD, PhD
Stanford University School of Medicine
Stanford,
CA
Plasmodium Falciparum Influences Erythropoiesis
SergeiDoulatov,PhD
Division of Hematology, Department of Medicine
Seattle,
WA
Ineffective Erythropoiesis in Myeloid Neoplasms
JOINT SESSION: Emerging Therapeutic Strategies Targeting Epigenetic, Transcriptomic, and Metabolic Mechanisms
Scientific Committee on Epigenetics and Genomics + Scientific Committee on Myeloid Neoplasia
Recent developments in therapeutic targeting of various mechanisms of epigenetic, transcriptomic, and metabolic vulnerabilities in cancer utilize novel technologies and may provide future breakthroughs. Given the extensive amount of knowledge derived from high throughput methodologies in the last decade, rational targeting is now possible, with sophisticated mechanistic studies to study the effects of targeting. This session will focus on novel research aimed at identifying and targeting these molecules, including novel targeting approaches such as heterobifunctional molecules and others.
CoChair:
Speakers:
Hannah JUckelmann,PhD
Frankfurt Cancer Institute
Frankfurt,
Germany
Novel Inhibitors of Transcriptional Mechanisms
Gerald R.Crabtree,MD
Stanford University
Stanford,
CA
Heterobifunctional Molecules Targeting Epigenetic Mechanisms
BenjaminCravatt,PhD
The Scripps Research Institute
San Diego,
CA
Inhibitors of RNAs and RNA Binding Proteins.
CourtneyJones,PhD
Cincinnati Children's Hospital
Cincinnati,
OH
Targeting Metabolic Vulnerabilities
JOINT SESSION: Molecular Characterization of Lymphomas in Children, Adolescents, and Young Adults
Scientific Committee on Blood Disorders in Childhood + Scientific Committee on Lymphoid Neoplasia
Dynamic advances in the molecular characterization of lymphomas continue to shape how these malignancies are classified and inform therapeutic targeting. This joint session will provide a state-of-the-science update on next-generation technologies used to explore that special group of lymphoma subtypes that are most prevalent in pediatric, adolescents, and young adults. The speakers represent experts in these methods and will highlight exciting applications in elucidating lymphoma biology (especially age-related differences in pathogenesis), including enhancing clinical management.
Dr. Lisa Roth will discuss ongoing efforts to delineate the genomic landscape of classic Hodgkin lymphoma (cHL). Historically, genetic evaluation of cHL has been limited by the scarcity of Hodgkin and Reed-Sternberg (HRS) cells in cHL tumors. This has been overcome in recent years using fluorescence-activated cell sorting to isolate HRS cells from cHL tissues and evaluation of circulating tumor DNA, which have revealed tumors with high mutational burden, complex structural variants, and genomic subtypes with distinct clinical and molecular characteristics. The applicability of these findings to develop prognostic biomarkers and novel therapeutics will be discussed.
Dr. Tomohiro Aokiwill discuss emerging single-cell technologies that have enabled better understanding of the comprehensive interactions within the cHL tumor microenvironment at an unprecedented resolution. Considering current pathogenesis models where HRS cells “recruit and re-educate” their microenvironment to create an immuno-suppressive milieu, cHL has emerged as one of the most exciting fields for application of these cutting-edge technologies. Dr. Aoki will summarize new insights gained using CyTOF, single-cell RNA sequencing and multiplexed imaging techniques, and discuss potential implications for clinical decisions.
Dr. Birgit Burkhardtwill provide a comprehensive update of recurrent genetic variants reported in Burkitt lymphoma (BL) in several recent studies. Covering both endemic and sporadic BL, Dr. Burkhardt will highlight the impact of patient age at diagnosis on molecular characteristics and its implications for pathogenesis. Incorporation of specific variants as potential biomarkers for risk group stratification in upcoming BL clinical trials will also be discussed.
Dr. Björn Chapuywill discuss novel (epi)genomic analyses employed to define molecular heterogeneity in B-cell lymphoma subtypes and identify clinically actionable alterations, with a focus on primary mediastinal large B-cell lymphomas (PBMLs). With biometric features that often overlap with cHL, PMBLs are distinguished by their typical manifestation in young female patients and sensitivity to PD-1 blockade. Dr. Chapuy will present evolving approaches to comprehensive genetic analysis used to inform and test response to therapies that target such mechanisms of immune escape.
CoChair:
Speakers:
Lisa GiulinoRoth,MD
Weill Cornell Medicine
New York,
NY
Genomic Landscape in Hodgkin Lymphoma
TomohiroAoki,MD, PhD
Princess Margaret Cancer Center
Toronto,
ON,Canada
Sequencing Technologies in Hodgkin Lymphoma
BirgitBurkhardt,MD,PhD
University Hospital Münster
Muenster,
Germany
Age-Related Molecular Changes in Burkitt Lymphoma
BjörnChapuy
Charité - University Medical Center Berlin, Campus Benjamin Franklin
Berlin,
Germany
Functional Genomics of Non-Hodgkin Lymphoma in Children, Adolescents, and Young Adults
JOINT SESSION: Newly Described Functions in the Vascular Space
Scientific Committee on Megakaryocytes and Platelets + Scientific Committee on Thrombosis and Vascular Biology
Dysregulated interactions between platelets, immune cells, endothelial cells, and their plasma environment underlie numerous age-related diseases. This joint session will provide an integrated view of the vascular space and will highlight the cellular and molecular mechanisms underlying diseases that primarily afflict the elderly. Specifically, the session will also on novel discoveries addressing how platelet and endothelial aging may affect neurodegenerative disorders and thrombotic disease, and immune thrombocytopenia (ITP), and will shed light into the role of fibrinolytic factors in shaping the pro-atherogenic plasma lipid profile.
Dr. Claus Nerlov, will discuss how aging affects hematopoietic stem cells (HSCs). He will describe how increased HSC platelet bias due to how age-related increases in TGFbeta signaling is an evolutionarily conserved feature of murine and human hematopoiesis. The role of HSC platelet bias in suppressing lymphoid cell production during aging and how TGFbeta receptor inhibition can increase the ability of aged HSCs to support antiviral immunity will also be discussed.
Dr. Nichola Cooper, will discuss the current understanding of ITP pathogenesis and how the results from novel treatments in ITP may depict different disease types in ITP. ITP is a common bleeding disorder with an increase in incidence after age 60. Understanding the disease phenotype and evolution is needed to improve patient outcomes. However, the diagnosis remains presumptive, and treatment is largely empiric, with many patients rotating through several treatments before having a platelet response.
Dr. Lisa Lesniewski will discuss the phenotype of the aging vasculature and the hematopathology underlying mechanisms and potential therapeutic strategies being explored to reverse arterial aging to reduce cardiovascular (CVD) risk in older adults. This is important since several factors contributing to dysfunction of the endothelium (i.e., oxidative stress and inflammation, deregulated nutrient sensing, and cellular senescence) increase with aging and could impact CVD risk.
Dr. Ze Zheng will discuss research demonstrating that hepatocytes are an unappreciated source of tissue-type plasminogen activator (tPA), sense metabolic stresses, and impact the production of tPA and its inhibitor PAI1, thereby influencing the extent of fibrinolysis in obesity. She will introduce findings that tPA binds directly to hepatocyte apoB, preventing it from being loaded with lipids and assembled into lipoproteins. Conversely, tPA's inhibitor, PAI1, has the opposite effect, sequestering free tPA and preventing its interaction with apoB to promote VLDL assembly and increase apoB-lipoprotein cholesterol levels.
CoChair:
Speakers:
ClausNerlov,PhD
University of Oxford
Oxford,
United Kingdom
Platelets and Aging
NicholaCooper,MD
Imperial College
London,
ENG,United Kingdom
New Insights in MK/PLT Functions and Diseases.
LisaLesniewski,PhD
University of Utah Health
Salt Lake City,
UT
Age-Related Endothelial Function
ZeZheng,MBBS,PhD
Medical College of Wisconsin; Versiti Blood Research Institute
Milwaukee,
WI
Novel Functions of Fibrinolytic Factors in Shaping the Pro-Atherogenic Lipid Profile in Plasma.
JOINT SESSION: The Fuel & Physiology of Regeneration
Scientific Committee on Hematopoiesis + Scientific Committee on Stem Cells and Regenerative Medicine
The regulation of hematopoietic stem cell (HSC) regeneration involves a sophisticated interplay between signals from the niche and the nuclear regulatory machinery. Extensive work has been done to identify many key players in both areas. However, conveying the signal to the nucleus is not sufficient without the “doers,” the machineries that execute the cellular processes critical for regeneration. Recent studies have identified several vulnerable processes in HSC physiology, such as proteostasis and energy metabolism, which become imbalanced during HSC exhaustion or dysfunction, i.e., processes involved in HSC culture expansion or aging. This session will closely examine the critical physiological processes and their interplay with other regulatory cues, including nutrient-derived signals (minerals and vitamins) crucial for maintaining healthy regeneration without malignant transformation.
Dr. Robert Signer, will discuss how protein homeostasis has emerged as fundamentally and preferentially important in HSCs. He will review how the protein homeostasis network is uniquely configured to promote hematopoietic stem cell self-renewal. Dr. Signer will further discuss how mechanisms of translational control, protein folding, and protein degradation are rewired throughout life to preserve stem cell fitness and will evaluate consequences of protein homeostasis disruption.
Dr. Marie-Dominique Filippi, will discuss the role of metabolism in HSC functions and how HSCs are highly responsive to changes in metabolite availability. New mechanisms will be presented on how HSC metabolic needs are remodeled during regenerative conditions. Additionally, Dr. Filippi will discuss the usage of branch chain amino acids as a new cell-autonomous metabolic checkpoint that influences HSC replicative lifespan.
Dr. Nina Cabezas-Wallscheid, will discuss how mouse and human HSCs and multipotent progenitors are metabolically regulated from intrinsic to dietary-derived metabolites. Through her work using integrated low-input multi-layer omics data, she will highlight research demonstrating distinct metabolic and epigenetic hubs that are essential in HSCs (and not for their downstream progenitors)
Dr. Britta Will, will discuss integrating nutrients into HSC regulation and iron homeostasis in HSCs. Her lab has uncovered a key role of the readily accessible intracellular labile iron pool in instructing HSC self-renewal. More recently, she has focused on identifying the molecular mechanisms of action, particularly focusing on metabolic and non-enzymatic pathways that rely on iron.
CoChair:
Speakers:
RobertSigner,PhD
University of California San Diego
La Jolla,
CA
Proteomic Health in Hematopoietic Stem Cells
Marie-DominiqueFilippi,PhD
Cincinnati Children's Hospital Research Foundation
Cincinnati,
OH
Energy Management in Hematopoietic Stem Cells
NinaCabezas-Wallscheid,PhD
ETH Zürich
Zürich,
Switzerland
Integrating Nutrients to Hematopoietic Stem Cell Regulation
BrittaWill,PhD
Albert Einstein College of Medicine
Bronx,
NY
Iron Homeostasis in Hematopoietic Stem Cells.
JOINT SESSION: Therapeutic Gene Editing of Stem Cells in Classical and Malignant Hematology
Scientific Committee on Bone Marrow Failure + Scientific Committee on Transplantation Biology and Cellular Therapies
Gene editing is a novel technology to change specific nucleotides or knockouts in cells, and these are starting to be used clinically. This joint-scientific committee session will include 4 talks that span from basic science to clinical use of gene-edited stem cell products and CAR-T products in malignant and classical hematology.
Dr. Justin Eyquem will discuss his latest work using novel gene editing technologies to improve CAR T-cell function and facilitate their manufacturing. He will present new gene edits associated with improved CAR T-cell functional persistence and novel types of vectors for the generation of CAR T cell in vivo.
Dr. Paulo Rio will present the latest results in optimizing novel genome editing tools, including prime editing, to correct hematopoietic stem cells (HSCs) from Fanconi Anemia (FA) patients. She will discuss the latest advances from her lab in optimizing prime editing technology to efficiently target long-term repopulating HSCs and correct the most common FA mutations in both cell lines and primary HSCs from FA patients.
Dr. Pietro Genovese will present the innovative “epitope editing” strategy for overcoming on-target/off-tumor toxicities in acute myeloid leukemia (AML) immunotherapy. Epitope mapping and library screenings have identified specific amino acid changes that have avoided antibody binding. These have now been introduced into HSPCs via base-editing techniques. Epitope-edited HSPC’s were resistant to CAR-T cell therapy, and enabled specific eradication of patient-derived AML xenografts. Dr. Genovese will discuss the potential of precision immunotherapy for relapsed/refractory AML, non-genotoxic conditioning approaches, and advances in multiplex engineering of HSPCs.
Dr. Julia Skokowa will review recent efforts to establish clinical genome editing to correct severe congenital neutropenia-associated mutations as well as gene editing efforts to inhibit mutated genes in patients' HSCs that may be applicable to other bone marrow failure syndromes. She will also discuss key considerations that are particularly important for gene therapy of pre-leukemic bone marrow syndromes, where gene editing of HSCs should be extremely safe so as not to potentiate the leukemogenic transformation of hematopoiesis. Finally, Dr. Skokowa will present her thoughts on the ethics of gene editing for pre-leukemic bone marrow failure.
CoChair:
Speakers:
JustinEyquem,PhD
University of California San Francisco
San Fransisco,
CA
New Gene Editing Technologies
PaulaRio,PhD
IIS-FJD, UAM
Madrid,
Spain
Gene Editing for Fanconi Anemia Bone Marrow Failure
PietroGenovese,PhD
Boston Children's Hospital
Boston,
MA
Stem Cell Gene Editing
JuliaSkokowa,MD, PhD
University Hospital Tübingen
Tübingen,
Germany
Gene Editing for Severe Congenital Neutropenia – Current Advances and Critical Considerations
Leveraging Single Cell Multi-Omics to Understand Mechanisms of Myeloid Lineage Expansion in Aging and Disease.
Scientific Committee on Myeloid Biology
Single cell multi-omic studies of normal and malignant hematopoiesis highlight how hematology remains an ideal testing ground for technologic innovation. Continued advancements in single cell sequencing and the analysis of these complex datasets have informed functional experiments that have enabled the field to improve its understanding of hematopoietic stem cell behavior and myeloid differentiation in response to aging, inflammation, and malignant transformation. This session will showcase innovative transcriptomic and functional genomic studies of the pathways that govern myeloid differentiation in response to aging, inflammation, and malignancy. The talks will focus on how advances in single cell lineage tracing have improved the fields’ understanding of hematopoietic stem cell commitment to the myeloid lineage early in life; explore how aging and inflammatory conditions impact myelopoiesis; and address how the tumor microenvironment can impact the function of mature myeloid cells.
Chair:
Esther A.Obeng,MD,PhD
St. Jude Children's Research Hospital
Memphis,
TN
Speakers:
ElisaLaurenti,PhD
University of Cambridge
Cambridge,
ENG,United Kingdom
Hematopoietic Stem Cell Commitment to the Myeloid Lineage
John E.Dick,PhD
Princess Margaret Cancer Centre, University Health Network
Toronto,
ON,CAN
Hematopoietic Stem Cell and Myeloid Progenitor Cell Response to Inflammation
Allon MosheKlein,PhD
Harvard Medical School
Boston,
MA
Myeloid Progenitor and Mature Neutrophil Responses in Cancer.
Metabolic Deregulation in Hematopoietic Neoplasia: Tumor, The Environment, and Therapies.
Scientific Committee on Hematopathology and Clinical Laboratory Hematology
Cellular metabolism and its role in the pathogenesis of hematologic malignancies is an emerging area of research. Recent studies implicate various cellular mechanisms by which oncogenic activation of metabolic pathways contribute to lymphoid and myeloid malignancies as well as their respective tumor environment. In this session, the speakers will discuss the role of deregulated cellular metabolism that contributes to lymphoid and myeloid malignancies and how they may provide novel insights with therapeutic relevance. The metabolic control of T cell differentiation and their function in immunity will also be discussed. This session highlights the opportunities for gaining novel mechanistic insights of hematologic malignancies through global metabolomic studies that has potential to impact the field of T-cell immunology, immunotherapies and facilitate translation to clinical practice.
Chair:
Megan S. SLim,MD,PhD
Memorial Sloan Kettering Cancer Center
New York City,
NY
Speakers:
Jürgen MaximilianRuland
Technical University of Munich
Munich,
Germany
Novel Insights in Metabolic Deregulation in Lymphoid Malignancies
PaoloGallipoli,MD
Queen Mary University of London
London,
United Kingdom
Targeting Metabolic Deregulation in Acute Myeloid Leukemia
AnandaGoldrath,PhD
Allen Institute
Seattle,
WA
Metabolic Control of T Cell Differentiation and Function in Tumor Immunity
Paradigm Shifts in Hemostasis: From Mechanisms to Therapies and Back
Scientific Committee on Hemostasis
Coagulation is not a linear process that ends at clot formation. Rather, coagulation is a network of ever-growing complexity with many mechanisms and pathways for regulation and feedback. The consequences of coagulation extend well beyond clot formation and into processes related to immunity, inflammation, vascular biology and regeneration. This session will highlight three examples for how bi-directional interactions from bench to bedside and back have paved the way to paradigm shifts in mechanistic insights, diagnosis, and treatment options for bleeding disorders and thrombotic complications.
Dr. Annette von Drygalski will discuss the most recent therapeutic paradigms in hemophilia. The continued unraveling of genetic and biochemical mechanisms underlying impaired blood clotting remains critical to inform the development of groundbreaking therapeutic strategies for Hemophilia A and B. Such strategies include extended half-life clotting factor preparations, non-factor-based molecules modifying hemostasis and, lastly, gene therapy. The new therapies have great potential to improve joint bleed prevention and reduce the sequelae of hemophilic arthropathy, which remains one of the most prominent aspects of clinical management in daily practice. Dr. von Drygalski will discuss pathophysiological mechanisms contributing to hemophilic arthropathy, new imaging modalities and joint outcome measures, paving the way for more targeted and individualized treatment strategies.
Dr. Daniël Verhoef will discuss the discovery and (pre)clinical development of a modified [PR1] recombinant form of coagulation factor X, called VMX-C001, which can bypass factor Xa direct oral anticoagulants (DOACs) in patients requiring immediate reversal of anticoagulation. It carries a unique 16 amino acid insertion that was derived from a snake venom factor X that makes VMX-C001 insensitive to inhibition by FXa DOACs. A single intravenous administration of VMX-C001 was shown to restore coagulation assays in animals and human volunteers on FXa-DOACs. VMX-C001 also prevented rivaroxaban induced bleeding in a primate liver injury model. VMX-C001 holds promise as an effective FXa DOAC reversal agent given its favorable half-life, short infusion time, FXa DOAC independent dosing and lack of a prothrombotic effect.
Dr. Cristina Puy will present a comprehensive exploration of coagulation factor XI dynamic interaction with diverse ligands, substrates, and endothelial cell receptors. Delving into the intricate mechanisms, Dr. Puy will elucidate factor XI pivotal role in modulating endothelial cell permeability and barrier function, shedding light on its implications in thrombotic and inflammatory conditions. This presentation will deepen our understanding of factor XI multifaceted involvement in health and disease.
Chair:
Laurent O.Mosnier,PhD
The Scripps Research Institute
La Jolla,
CA
Speakers:
Annettevon Drygalski,MD, PharmD, RMSK
University of California San Diego (UCSD)
SAN DIEGO,
CA
Paradigm Shifts in Hemophilia.
DaniëlVerhoef,MSc, PhD
VarmX B.V.
Leiden,
Netherlands
Paradigm Shifts in the Reversal of DOACs
CristinaPuy Garcia,PhD
Oregon Health and Science University
Portland,
OR
New Mechanisms That May Fuel the Paradigm Shifts of the Future
Proteo-Genomics to Better Study Multiple Myeloma Biology and Evolution
Scientific Committee on Plasma Cell Neoplasia
Cancer proteogenomics provides new biological and diagnostic knowledge that can improve our understanding of malignant transformation and therapeutic outcomes. This area is new in plasma cell neoplasia. In this session the speakers will discuss how proteogenomics can lead to a better study of multiple myeloma (MM) biology and support the development of novel therapeutic targets in MM.
Dr. Jan Krönke will discuss the impact of proteogenomic studies on our understanding of MM biology. He will outline how proteomics improve risk stratification, and reveal deregulated proteins and pathways that can be exploited for new therapies in MM.
Dr. Francesco Maura will present the genomic landscape of MM and its precursor conditions, with a particular focus on the temporal acquisition of various combinations of genomic drivers. He will highlight the relevance of these genomic patterns in predicting MM progression and identifying the most effective immunotherapy for MM patients.
Dr. Fabiana Perna will describe a strategy for probing the MM surface proteome (surfaceome) with mass-spectrometry and transcriptomic analyses to identify novel immunotherapeutic targets. She will discuss the contribution that the surfaceome makes to MM biology as well as the pre-clinical development of novel chimeric antigen receptor platforms for MM.
Chair:
PaolaNeri,MD,PhD
Arnie Charbonneau Cancer Institute, University of Calgary
Calgary,
AB,Canada
Speakers:
JanKronke,MD
Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health
Berlin,
Germany
Defining the Proteomic Landscape of Multiple Myeloma
FrancescoMaura,MD
University of Miami
Palmetto Bay,
FL
Genomic Drivers Involved in Myeloma Progression and Development of Resistance
FabianaPerna,MD, PhD
H. Lee Moffitt Cancer Center and Research Institute
Tampa,
FL
Proteo-Genomics to Better Study Cell Surfaceome in Multiple Myeloma
Understanding the Impact of Donor and Recipient Metabolic Variability on Blood Transfusion Outcomes
Scientific Committee on Transfusion Medicine
Blood transfusion requires the donation of blood products from a diverse array of individuals with unique genetics and environmental inputs. This results in the quality and overall behavior of the blood products being less standardized and predictable, with direct consequences on transfused recipients. This session will focus on how recently recognized unique genetic and environmental backgrounds of both the blood donor and the transfusion recipient influence the outcomes of patients. Newly applied metabolic tools reveal metabolic variability in donors and recipients, shedding light on fundamental aspects of these differential responses of transfusion in patients, which could guide future strategies for more personalized and effective blood transfusions.
Chair:
Cassandra DorothyJosephson,MD
Johns Hopkins All Children’s Hospital
St. Petersburg,
FL
Speakers:
AngeloD'Alessandro,PhD
University of Colorado Anschutz Medical Campus
Aurora,
CO
Blood Donor Genetics and Biology Impact Red Blood Cell Transfusion Outcomes
MoritzStolla,MD
Bloodworks and University of Washington, Pathology and Laboratory Medicine
Seattle,
WA
Unveiling Platelet Metabolism: Implications for Storage and Transfusion
CherylLobo,PhD
Laboratory of Blood-Borne Parasites, Lindsley F. Kimball Research Institute, New York Blood Center
New York,
NY
Impact of RBC Metabolism on the Disease Outcomes of Transfusion Dependent Patients
Scientific Spotlight Sessions
Fulfilling the Promise: Pluripotent Stem Cells as Models for Human Blood Development and Disease
Generation of self-renewing hematopoietic stem cells (HSCs) from human pluripotent stem cells (PSCs) for transplantation and disease modeling has been a long-standing goal in the field, but has been hampered by the difficulty in differentiating bona fide HSCs in culture. In recent years there has been tremendous progress in the field, and investigators have been able to define the developmental cues to direct mesodermal differentiation to definitive HSC fate rather than defaulting to embryonic type progenitors. These studies have been further fueled by the advances in single cell transcriptomic technologies, which has made it possible to compare in vitro HSC development to human HSCs developing in vivo. Advances in this area of research will be highlighted in this session.
CoChair:
Speakers:
Elizabeth W.Ng,MD
Kansas City Cancer Center
Overland Park,
KS
Hematopoietic Stem Cell Development from Human Pluripotent Stem Cells
EiriniPapapetrou,MD,PhD
Icahn School of Medicine at Mount Sinai
New York,
NY
Modeling Blood Disorders Using Human Pluripotent Stem Cells
Biology Underlying Disparities in Lymphoid Malignancies
Significant disparities in outcomes have been described for several lymphoma subtypes, most notably related to race and HIV status. Although socioeconomic factors often play a role, new approaches are needed to determine whether distinct pathogenic mechanisms underlie such disparities. The modern era has been marked by major advances in understanding lymphoma pathobiology, but populations affected by disparities are woefully under-represented in most of these pivotal studies. This session will highlight recent, innovative work dedicated to closing this knowledge gap and identifying molecular targets for improving outcomes in vulnerable populations.
CoChair:
Speakers:
Christopher R.Flowers,MD, MS
The University of Texas MD Anderson Cancer Center
Houston,
TX
Tumor Sequencing to Investigate Disparities in Lymphoma
WendyCozen,DO, MPH
UCI, School of Medicine
Orange,
CA
Tumor Microenvironment Profiling to Investigate Disparities in Hodgkin Lymphoma and Multiple Myeloma
Inflammation as a Regulator of Hematopoietic Homeostasis in Disease and Clonal Selection
Hematopoietic stem and progenitor cells (HSPCs) are responsible for integrating inflammatory cues into cellular responses and establishing a demand-adapted axis between peripheral stresses and hematopoietic responses in the bone marrow. This session will describe how the pro-inflammatory environment/response and systemic inflammation act on and subsequently shape HSPC and hematopoietic homeostasis.
CoChair:
Speakers:
HitoshiTakizawa,PhD
Kumamoto University
Kumamoto,
Japan
Inflammation As a Regulator of Hematopoietic Homeostasis in Disease
SerineAvagyan,MD, PhD
University of California San Francisco
San Francisco,
CA
Inflammation As a Regulator of Hematopoietic Homeostasis in Clonal Selection
Iron at the Crossroads Between Erythropoiesis and Megakaryopoiesis
This session will highlight the importance of iron balance for a healthy and effective erythropoiesis and thrombopoiesis. All mammalian cells rely on iron for normal functioning, with the erythropoietic compartment consuming the majority given the high iron requirements for hemoglobin synthesis. Recent evidence on the crosstalk between erythropoiesis and iron metabolism shed light on the consequences of insufficient as well as excess iron and heme on erythroid lineage proliferation and differentiation. In this session, the contribution of heme and iron excess to ineffective erythropoiesis will be described, with a focus on erythroid cell trajectories during differentiation, metabolic shifts, and erythroid cell-macrophage interaction within erythroblastic islands (EBIs). The session will also describe the role iron plays in other hematopoietic processes, including megakaryopoiesis and platelet formation.
CoChair:
Speakers:
Janis L.Abkowitz,MD
University of Washington
Seattle,
WA
Role of Heme and Iron in Effective and Ineffective Erythropoiesis
Radek C.Skoda,MD
University Hospital Basel
Basel,
Switzerland
Impact of Iron Availability on Megakaryopoiesis
Phylogenetic Reconstruction of Hematopoiesis
Hematopoiesis is a complex and highly regulated process that has been increasingly understood through advances in genetics, epigenetics, and single-cell genomics technologies. Recent work has focused on increasingly nuanced and detailed phylogenies of hematopoietic cells in normal and aged individuals, and multidimensional understanding of phylogenetic trees of stem cells, progenitors, and mature progeny. Genomics, epigenetics, advanced computational analyses, large scale datasets, and single-cell approaches are all integral in this effort. This session will present some of the latest advances in the field and serve to educate the audience of how these may inform our understanding of physiological and pathological mechanisms in hematopoiesis.
CoChair:
Speakers:
JyotiNangalia,MBBChir
Wellcome Sanger Institute
Hinxton,
United Kingdom
Incorporating Genetic and Epigenetic Marks in Phylogenetic Reconstruction of Blood Cells
CharlesGawad,MD
Stanford University
Memphis,
TN
Novel Single-Cell Genomics Technologies to Reconstruct Phylogenetics of Human Blood Cells
Scientific Symposia
Cellular Heterogeneity and Relationship to Clinical Outcomes
Cellular therapies are quite heterogeneous by nature, but regulatory and industry groups have focused on defining particular products with "critical product attributes" while minimizing heterogeneity. This session will highlight the potential benefits of cellular heterogeneity, in both immune effector cells and within post-transplant cell populations.
Chair:
CraigByersdorfer,MD
University of Pittsburgh
Pittsburgh,
PA
Speakers:
ZinaidaGood,PhD
Stanford University School of Medicine
Stanford,
CA
Heterogeneity of CD19 CAR T Cells
JuliaCarnevale,MD
University of California San Francisco
San Francisco,
CA
Purposeful Heterogeneity of CAR T Cells
MeganLevings,PhD
University of British Columbia, Canada
Vancouver,
BC,CAN
Heterogeneity of Cells in Transplantation
Interface of Complement and Coagulation
The complement system and coagulation pathways are the main pillars of immunity and hemostasis respectively that undergo significant activation with injury. While appearing distinct, it is recognized that significant crosstalk exists between the two systems and recently established molecular mechanisms provide insights into a wide variety of disorders. This session will focus on new molecular links identified in complement activation in specific and highly relevant clinical disorders.
Chair:
DavidKavanagh,PhD
New Castle University
Newcastle Upon Tyne,
United Kingdom
Speakers:
DavidKavanagh,PhD
New Castle University
Newcastle Upon Tyne,
United Kingdom
Complement and the Prothrombotic State
EfthymiaVlachaki,MD, PhD
Hippokrateon Hospital
Thessaloniki,
Greece
Complement Activation and Preclampsia
Lubka TRoumenina,PhD
INSERM UMRS1138 Cordeliers Research Center
Paris,
France
Sickle Cell Disease and Complement Activation
Interrogating the Impact of the Intestinal Microbiome on Transplant and Cellular Therapies
Fundamental advances have been achieved in the treatment of patients with hematologic malignancies through transplant and cellular therapy (TCT), including hematopoietic cell transplant and chimeric antigen receptor (CAR) T cell therapy. However, the therapies have limitations, such as relapses and toxicity. TCT outcomes have been associated with the intestinal microbiome. This session will focus on the intestinal microbiome in relation to TCT, from correlative research to interventional studies.
Chair:
MelodySmith,MD,MS
Stanford University School of Medicine
Stanford,
CA
Speakers:
FlorentMalard,M.D., Ph.D.
Sorbonne Université, Hôpital Saint-Antoine, AP-HP, Service d'Hématologie Clinique et Thérapie Cellulaire,Centre de Recherche Saint-Antoine UMRs938
Paris,
France
Fecal Microbiota Transplant As a Strategy to Mitigate Infection and Gvhd Following TCT
Lawrence ADavid,PhD
Duke University
Durham,
NC
Deciphering Nutritional Intake from Metagenomic Data Using Computational Tools
TessaAndermann,MD,MPH
University of North Carolina, Chapel Hill
Chapel Hill,
NC
Impact of Antibiotic Exposure on Outcomes Following TCT
Newly Discovered Functions of Megakaryocytes and Platelets
This session will reveal new mechanisms of diseases related to platelet formation and function. Specifically, it will address glycosylation in megakaryocytes (Mks)/platelet functions and diseases; and highlight new insights in thromboinflammation, functions, and diseases of Mks and platelets.
Chair:
AlessandraBalduini,MD
Tufts University
Medford,
MA
Speakers:
Karin M.Hoffmeister,M.D.
Versiti Blood Research Institute, Milwaukee, WI
Milwaukee,
WI
Glycans and New Pathogenic Mechanisms of ITP
TobiasPetzold,MD,MSc
Charité – Universitätsmedizin Berlin
Berlin,
Germany
Regulation of Platelet Function During Immobilty
Anna S.Nam,MD
Weill Cornell Medicine
New York,
NY
Platelet ER Stress in Thrombosis
Placing the Brakes on Accelerated Aging
Hematologic disorders disproportionately affect older adults; despite this, our understanding of the implications of age on the pathogenesis and treatment of these diseases remains limited. The geroscience field is actively investigating geriomics to aid in distinguishing biological and chronological aging. This session will highlight biological aging assessments for hematologic disease which will be crucial for the identification of targets and development of therapies for this specific population.
Chair:
AshleyRosko,MD
The Ohio State University
Columbus,
OH
Speakers:
ElsMansell,PhD
Erasmus Medical Center
Rotterdam,
Netherlands
Ageing of Hematopoietic Stem Cells and Their Niche
Christin EBurd,PhD
Ohio State
Columbus,
OH
Geroscience and Geri-Omics in Hematologic Malignancies
Marcel R.M.van den Brink,MD, PhD
City of Hope National Medical Center
Duarte,
CA
Targeting Rejuvenation Therapies to Decelerate Aging
Special-Interest Sessions
Artificial Intelligence in Hematology: From Generative AI to Ethics and Applications
The session will address important and timely topics related to the application of artificial intelligence (AI) to hematology, ranging from generative AI's potential and pitfalls, modern ethical consideration for AI in biomedical research and examples of practical use of AI in hematology research and clinical care.
Chair:
OlivierElemento,PhD
Weill Cornell Medicine
New York,
NY
Speakers:
JamesZou,PhD
Stanford University
Stanford,
CA
The Potential and Pitfalls of Generative AI in Basic and Clinical Research
CamilleNebeker,EdD
University of California San Diego
San Diego,
CA
From Principles to Practice: Ensuring Ethical Integrity in AI-Driven Biomedical Research
ClaudiaHaferlach,MD
MLL Munich Leukemia Laboratory
Munich,
Germany
The Application of Artificial Intelligence in Hematological Diagnostics
ASH Clinical Practice Guidelines on Acute Lymphoblastic Leukemia (ALL) in Adolescents and Young Adults
This session will preview recommendations for initial therapy and management of remission and relapse in adolescents and young adults with ALL.
Chair:
SumitGupta,MD, PhD
Hospital for Sick Children
Toronto,
ON,Canada
Speakers:
JulieWolfson,MD, MSHS
The University of Alabama at Birmingham
Birmingham,
AL
Management of Frontline ALL in AYA
Jennifer L.McNeer,MD
University of Chicago
Chicago,
IL
Management of Frontline ALL in AYA
Kristen M.O'Dwyer,MD
University of Rochester
Rochester,
NY
Management of Refractory and Relapse of ALL in Adolescents and Young Adults
Lena EWinestone,MD
University of California San Francisco
San Francisco,
CA
Management of Refractory and Relapse of ALL in Adolescents and Young Adults
ASH Clinical Practice Guidelines on Amyloidosis
This session will review the scope and goals of the upcoming guidelines on amyloidosis, and will provide insights on risk factors, selecting a target site versus a surrogate site for diagnostic biopsies, and using Congo Red stain screening.
Chair:
VishalKukreti
University Health Network
Toronto,
ON,Canada
Speakers:
AngelaDispenzieri,MD
Mayo Clinic
Rochester,
MN
Target Site vs. Surrogate Site Biopsy for Diagnosis
JoselleCook,MBBS
Mayo
Rochester,
MN
Increasing Awareness of Risk Factors for AL Amyloidosis
NareshBumma,MD
The Ohio State University
Columbus,
OH
Congo Red Stain Screening for AL Amyloidosis
HiraShaikh,MD
University of Iowa Caver College of Medicine
Coralville,
IA
Target Site Vs. Surrogate Site Biopsy for Diagnosis
ASH Clinical Practice Guidelines on Pediatric Venous Thromboembolism (VTE)
This session will highlight new and revised recommendations for the treatment of VTE in pediatric patients, including addressing asymptomatic VTE, duration of therapy for provoked and unprovoked VTE, and use of anticoagulants.
Chair:
PaulMonagle
University of Melbourne Royal Children's Hospital
Parkville,
VIC,Australia
Speakers:
LeslieRaffini,MD
Children's Hospital of Philadelphia
Philadelphia,
PA
Why Revise the Guidelines?
RukhmiBhat,MD,MS
Lurie Children's Hospital
Chicago,
IL
Asymptomatic VTE in Pediatric Patients
MarisolBetensky,MD
Johns Hopkins All Children's Hospital
Saint Petersburg,
FL
Duration of Therapy for Provoked and Unprovoked VTE in Pediatric Patients
TinaBiss,MD
The Newcastle upon Tyne Hospitals NHS Trust
Newcastle Upon Tyne,
ENG,United Kingdom
Use of Anticoagulants in Children
ASH Quality Improvement Champions
This new session merges the ASH Choosing Wisely Champions and the ASH Guideline Implementation Champions into a single, 90-minute session. Speakers will be selected from a pool of applicants. In addition to projects that combat overuse (previously the focus of the Choosing Wisely Champions session) and projects that highlight successful guideline implementation strategies (previously the focus of the Guideline Implementation Champions session), the call for applications for this session considers any quality improvement project (e.g., combating underuse, improving stewardship of resources, improving processes, reducing or eliminating healthcare disparities, etc.). The goal of this change is to expand opportunities to highlight high-quality quality improvement work while concentrating the focus into a single session.
CoChair:
Speakers:
JosieFernandez Sanchez,MD
Texas Children’s Hospital, Baylor College of Medicine
Houston,
TX
Standardizing Emergency Department Management of Iron Deficiency Anemia from Heavy Menstrual Bleeding
PaoloLopedote,MD
City of Hope National Medical Center
Monrovia,
CA
Reduced Blood Transfusions in Patients with Chronic Liver Disease Undergoing Paracentesis
Asinamai MNdai,BPharm, MS
University of Florida Health Physicians
Gainesville,
FL
Optimized Management of Hemophilia in the Emergency Department
Early Faculty Career Development Session
In this Junior Faculty Career Development Session, attendees will hear a series of lectures focused on Mentorship. These didactic lectures will feature mentoring experts sharing their experiences in how to receive, provide, and optimize mentoring. Mentor/Mentee relationships can be hard to foster, and in this session, we will focus on empowering junior faculty with the tools to get the most out of this relationship. Junior faculty will hear from mentors and mentees both in the clinical and basic research fields and gain a better understanding on what it is to be a good mentor and mentee.
CoChair:
Speakers:
Betty S.Pace,MD
Augusta University
Augusta,
GA
Identifying a Mentor and Optimizing the Mentor/Mentee Relationship, How to be a Good Mentee?
Adam ScottKittai,MD
The Ohio State University
Columbus,
OH
Identifying a Mentor and Optimizing the Mentor/Mentee Relationship, How to be a Good Mentee?
JosephMikhael,MD, MeD, FRCPC, FACP
Translational Genomics Research Institute
Phoenix,
AZ
The Warning Signs of a Problematic Mentoring Relationship and How to Fix it
ShannonElf,PhD
The University of Chicago
Chicago,
IL
The Warning Signs of a Problematic Mentoring Relationship and How to Fix it
LeidyIsenalumhe
Moffitt Cancer Center
Lutz,
FL
Transitioning from Being a Mentee to Becoming a Mentor
RaquelEspin Palazon,PhD
Iowa State University
Ames,
IA
Transitioning from Being a Mentee to Becoming a Mentor
Medical Educators Symposium
The Medical Educators Symposium (previously called the Hematology Course Directors Workshop) is open to all medical educators across the medical student, resident, and fellow continuum. The Medical Educators Symposium highlights cutting edge teaching techniques and theories while also showcasing participants of the ASH Medical Educators Institute. The symposium is two hours long and will begin with an hour of general sessions focused on medical education principles and then followed by simultaneous breakout sessions that happen twice.
Chair:
Hetty E.Carraway,MD,MBA
Cleveland Clinic
Cleveland,
OH
Speakers:
AlisonLoren,MD
University of Pennsylvania
Philadelphia,
PA
General Session 1: Paving a Career in Medical ѻý & Scholarship
MeganDupuis
Vanderbilt University
Durham,
NC
General Session 2: Utilizing Humanities to Influence and Tailor Hematology Curriculum for Adult Learners
LaylaVan Doren
Yale University
New York,
NY
General Session 3: Incorporating Health Equity ѻý in UME/GME Curriculum
Alexander ABoucher,MD
University of Minnesota
Minneapolis,
MN
General Session 3: Incorporating Health Equity ѻý in UME/GME Curriculum
BeverlySchaefer,MD
University of Buffalo
Buffalo,
NY
Breakout 1: Challenges for Course Development
Ariela L.Marshall,MD
University of Minnesota
Rochester,
MN
Breakout 2: Developing Your Teaching Portfolio
Jason AFreed,MD
Beth Israel Deaconess
Boston,
MA
Breakout 3: Cutting-Edge Technology in ѻý Delivery
Thomas W.LeBlanc,MD, MA, MSH
Duke Cancer Center
Durham,
NC
Breakout 4: Developing a Palliative Care/Difficult Discussion Curriculum
Race and Ancestry in Precision Medicine
Race and ancestry, historically, have been poorly considered in basic and translational research design and clinical diagnoses. This session will describe how race and ancestry can inform hematology research conduct, specifically in clinical and genetic population profiling, interpretation of common hematologic tests, development of diagnostics, and overall precision medicine. The speakers selected in this session have incorporated race and ancestry in their own research and will be sharing their insights to help educate hematology investigators and clinicians understand how to consider race and ancestry into their own research and practice.
CoChair:
Speakers:
KeoluFox
University of California, San Diego
San Diego,
CA
Incorporating Indigenous Perspectives into Population Genetics
Ann-KathrinEisfeld,MD
The Ohio State University Comprehensive Cancer Center
Columbus,
OH
Risk Re-Stratification Based on Black AML Patient Exome Data
MaureenAchebe
Brigham and Women's Hospital
Boston,
MA
How Inappropriate Reference Ranges Can Propagate Systemic Racism
Sickle Cell Disease Centers Session
To ensure high-quality care for patients with sickle cell disease (SCD), it is imperative that providers and SCD care leaders have the tools to establish comprehensive clinical care centers for patients with SCD. Over the last several years, ASH has developed a program and blueprint for the creation of sickle cell disease centers. This special interest session to address how sickle cell disease care centers can leverage the recent, relevant changes in quality metrics to deliver high quality care and demonstrate the financial value of centers to institutional leaders.
CoChair:
Symposium for Mid-Career Hematologists
This symposium aims to guide the audience through the common challenges faced by mid-career hematologists. Some examples of unique challenges for mid-career hematologists include negotiating the first leadership position, principles of leadership, promotion, strategies for managing individuals and teams, conflict management, setting up a successful research program, time management, funding beyond career development awards, performance and compensation metrics, self-care and opportunities to contribute to the Society’s mission. Speakers will include a diverse pool of successful physicians and scientists from academia, regulatory agencies, and the pharmaceutical industry. It is envisioned that this educational session will be organized by a steering committee of Society members who will identify a longitudinal curriculum for the session and speakers and topics.
Chair:
Juan PabloAlderuccio,MD
Sylvester Comprehensive Cancer Center University of Miami
Miami,
FL
ShrutiChaturvedi,MBBS
Johns Hopkins University
Baltimore,
MD
Speakers:
Ruben A.Mesa,MD
Atrium Health Wake Forest Baptist
Winston-Salem,
NC
Negotiating Your First Leadership Position
Allison A.King,MD,PhD,MPH
Washington University School of Medicine
Saint Louis,
MO
Negotiating Your First Leadership Position
Robert F.Sidonio, Jr.,MD, MSc
Emory University
Atlanta,
GA
Your Next Job - How to Identify Academic Opportunities with the Best Payback
Jeffrey DLebensburger,DO
University of Alabama at Birmingham
Birmingham,
AL
Your Next Job - How to Identify Academic Opportunities with the Best Payback
NinaShah,MD
AstraZeneca
South San Francisco,
CA
Making the Jump - Careers Outside Academia
David P.Steensma,MD, FACP
Ajax Therapeutics
Lincoln,
MA
Making the Jump - Careers Outside Academia
Symposium on Quality: Treating Fairly - The Role of Quality Improvement in Combating Health Care Disparities
This year's Quality Symposium will focus on practical strategies for combatting healthcare disparities. First, Dr. Melissa Creary will discuss the Michigan Social Health Interventions to Eliminate Disparities (MSHIELD) program, a statewide data-driven, community-partnered, and equity-centered quality improvement effort. Then Dr. Michelle Sholzberg will review the development and impact of the "Raise the Bar" project, which aims to eliminate disparities in the recognition and management of iron deficiency by adjusting reference ranges. The session will conclude with a talk by Dr. Thomas Greg Knight on mitigating the impact of financial toxicity in patients with hematologic malignancies.
CoChair:
Speakers:
MelissaCreary
University of Michigan School of Public Health
Ann Arbor,
MI
MSHIELD - Michigan Social Health Interventions to Eliminate Disparities
MichelleSholzberg,MDCM, MSc
University of Toronto
Toronto,
ON,Canada
Raise the Bar - Combatting Disparities in the Recognition and Management of Iron Deficiency
Thomas G.Knight,MD
Atrium Health
Charlotte,
NC
Cancer and Poverty - Mitigating the Impact of Financial Toxicity in Patients with Hematologic Malignancies
Systems-Based Hematology ѻý and Networking Session: Anticoagulation Stewardship and AI-Assisted Management
This session will feature two talks on systems-level approaches to anticoagulation management, followed by a networking session where attendees will meet with the speakers and with established systems-based hematologists over light hors d'oeuvres and drinks. The first talk with feature Dr. Greg Barnes discussing how to improve systems-level management of anticoagulants within and across care settings. For the second talk, Dr. Damon E. Houghton will discuss the use of artificial intelligence (AI) and machine learning (ML) in the context of anticoagulation management.
Chair:
CamilaMasias,MD,MPH
Miami Cancer Institute
Miami,
FL
Speakers:
Geoffrey DBarnes,MD, MSc
University of Michigan
Ann Arbor,
MI
Improving Systems-Level Management of Anticoagulants Within and Across Care Settings
Damon E.Houghton,MD,MS
Mayo Clinic Rochester
Rochester,
MN
Artificial Intelligence (AI) and Machine Learning (ML) in the Context of Anticoagulation Management
Training Program Directors Workshop
The Training Program Director’s Workshop is held each year before the ASH annual meeting and is designed for training program directors, associate program directors, and others involved with hematology training. The workshop is designed for hematology program directors to share lessons learned, best practice, and explore opportunities to improve their leadership skills. Through experiential learning techniques, breakout sessions, and interactive lectures, program directors can learn from peers and build their network. At this year’s TPDW, we will focus on three opportune topics. First, we will discuss how to design and implement innovative curriculums which can prepare trainees to excel at various aspects of hematology oncology practice beyond just knowledge of the subject matter. Examples of such curriculums include ‘leadership training’, ‘how to be a good educator’, and ‘business of hematology-oncology’. Second, we will focus on best practices for a training program to leverage social media and build their ‘brand’. Lastly, we will discuss practical ways in which programs can help trainees land their dream job.
Chair:
PallawiTorka
Roswell Park Cancer Center
Buffalo,
NY
Speakers:
ScottMoerdler,MD
Rutgers Cancer Institute
New Brunswick,
NJ
Innovative Fellowship Curriculum
Layla NVan Doren,MD, MBA
Yale School of Medicine
New Haven,
CT
Innovative Fellowship Curriculum
Angela CWeyand,MD
University of Michigan
Ann Arbor,
MI
Leveraging and Enriching Social Media
GeraldHsu,MD,PhD
University of California, San Francisco
San Francisco,
CA
Best Practices to Support Fellows in the Job Search
SunandanaChandra,MD
Northwestern University
Chicago,
IL
Best Practices to Support Fellows in the Job Search
66th ASH Annual Meeting and exposition
Registration for ASH members will open on July 17, 2024, at 11:00 a.m. Eastern time.
Registration for non-members, groups, exhibitors, and media opens on August 7, 2024.