Education Spotlight Sessions
The following contains information pertaining to the 2024 ASH Annual Meeting. Preliminary session information for the 2025 ASH Annual Meeting will be available in June.
Education Spotlight sessions are intended for a smaller audience to focus on a highly specialized topic and to facilitate interactive discussion on current challenges and controversies in a particular clinical field.
Unless otherwise noted, all sessions will take place in person and stream simultaneously on the virtual platform. Session recordings will be available on demand on the virtual platform.
Asparaginase in ALL/LBL: Balancing the Risk/Benefit of New Efficacious Preparations
Asparaginase is a considered a cornerstone of therapy for acute lymphoblastic leukemia/lymphoblastic lymphoma (ALL/LBL). Since its therapeutic potential was first described in the 1960s, the incorporation of asparaginase into treatment protocols beginning in the mid-1970s was associated with significant improvements in outcomes. Over the past several decades, asparaginase formulations have undergone important advancements. The pegylation of E.coli-derived asparaginase enabled less frequent administration, improving patient convenience. The development of asparaginase from Erwinia chrysanthemi provided a non-cross-reactive alternative for patients who develop hypersensitivity to E. coli asparaginase, allowing them to complete their full treatment course safely. More recently, modification to the PEG linker have resulted in a product with a substantially longer in vivo half-life. The introduction of a recombinant form of Erwinia asparaginase has addressed significant drug shortages associated with the native preparation. Despite these advances, like all anti-cancer drugs, asparaginase preparations are associated with toxicities, many of which are distinct from other agents in patients’ treatment regimen. In this session, we will tackle the complexities of balancing the demonstrated benefits of asparaginases with their unique toxicities.
Dr. Birgitte Albersen will focus on hypersensitivity reactions to asparaginase. As a foreign protein, asparaginase can illicit an immune response resulting in life-threatening allergic reactions and neutralization of the drug. Dr. Alberten will discuss the incidence and manifestations of antibody-mediated hypersensitivity reactions, the role of therapeutic drug monitoring, and potential means to distinguish antibody-mediated from infusion reactions. She will also discuss management strategies, emphasizing when it is necessary to switch from E. coli-derived to Erwinia-derived asparaginase.
Dr. Marlise Luskin will review the spectrum of other adverse events that can occur with asparaginase including pancreatitis, hyperglycemia, hyperlipidemia, and thromboses. Dr. Luskin will highlight known risk factors for specific toxicities such as age and obesity and discuss potential prevention strategies and management approaches. Additionally, Dr. Luskin will address criteria for safely rechallenging patients with asparaginase following toxicity.
Chair:
Rachel Rau
Seattle Children's Hospital
Seattle, Washington, United States
Speakers:
Birgitte Klug Albertsen Sr
Aarhus University Hospital and Aarhus University
Aarhus, Central Denmark Region, Denmark
Asparaginase Hypersensitivity Incidence, Manifestations, and Management
Marlise Luskin
Dana-Farber Cancer Institute
Boston, Massachusetts, United States
Beyond Hypersensitivity: The Gamut of Other Asparaginase Associated Toxicities
How to Prevent and Manage infections in Immunocompromised Patients in the Era of Immunotherapy and Growing Antibiotic Resistance?
Chair:
Lidia Gil
Speakers:
Randy Taplitz
City of Hope National Medical Center
Duarte, California, United States
Measures to Minimize Infection Risk in Immunocompromised Patients after Cellular Therapies - How, for Whom, for How Long?
Miguel Angel Perales
Memorial Sloan Kettering Cancer Center
New York, New York, United States
Protection Without Complete Disruption (of the microbiome): Management of Febrile Neutropenia in Immunocompromised Patients in 2025
Joint Session with ASPHO: Transition to Adult Care in Malignant and Classical Hematology
Chair:
Deepa Manwani
Speakers:
Jerlym Porter
St. Jude Children's Research Hospital
Memphis, Tennessee, United States
Quality after Quality Improvement Projects for Improved Transition: Lessons Learned in Sustainability OR Predictors of Success
David Robert Freyer
Children's Hospital Los Angeles
Los Angeles, California, United States
Models and Importance of Successful Transition in Leukemia/Lymphoma Survivors
The Changing Face of Chronic Myelogenous Leukemia
Chronic myelogenous leukemia management has evolved significantly over the past two decades with the approval and development of multiple TKIs including ATP binding site TKIs and recently, the approval of a myristoyl pocket inhibitor, Asciminib. The recent approval of asciminib in the upfront setting continues to change the treatment paradigm for this disease. However, questions remain regarding TKI selection in the upfront setting and beyond. Investigation is ongoing focusing on questions surrounding TKI selection and strategies evaluating combination therapy are emerging. Dr. Jorge Cortes will discuss current recommendations for frontline treatment selection and Dr. Fancois-Xavier Mahon will discuss current data around treatment free remissions and other TKI management strategies, discussing management of long-term TKI-related toxicities (in adult and pediatric patients). Of note, the speakers will ensure the pediatric perspective is incorporated as well.
Chairs:
Gabriela Hobbs
Harvard Medical School
Cambridge, Massachusetts, United States
Gabriela Hobbs
Massachusetts General Hospital
Boston, Massachusetts, United States
Speakers:
Jorge Cortes
Georgia Cancer Center at Augusta University
Augusta, South Carolina, United States
Frontline Treatment Selection for CML in 2025
Francois-Xavier Mahon
Institut Bergonié and Bordeaux university
Bordeaux, Nouvelle Aquitaine, France
Can I Stop Taking My TKI Yet?
Transfusion Medicine for Practicing Hematologists: How to Prevent and Treat Potentially Fatal Reactions in Sickle Cell Disease
Over the decades, due to advances in infectious disease testing, blood and blood component transfusions have become remarkably safe; however, non-infectious complications remain a concern. Some of these complications are uncommon and may, therefore, be overlooked in clinical practice. This session will focus on some of these uncommon but potentially fatal complications seen in patients with sickle cell anemia (SCA), many of whom are transfusion dependent.
Dr Chou will review the role of genetic testing in SCA, where Red blood cell (RBC) transfusions are a critical, often lifesaving therapy. However, this population faces a disproportionately high risk of alloimmunization, leading to serious complications such as delayed hemolytic transfusion reactions (DHTRs). In this session, she will explore clinical case studies that illustrate how molecular technologies can be used to reduce alloimmunization and DHTR risk. She will also discuss strategies for selecting compatible donors for patients with complex alloantibody profiles and how DNA-based matching techniques can enhance transfusion safety and improve clinical outcomes.
Dr Weiss will discuss hyperhemolysis syndrome (HHS), which is a rare yet critical condition that poses significant risks of morbidity and mortality associated with blood transfusions. Through an examination of several clinical case studies from the transfusion service perspective, attendees will gain insights into the complexities and nuances of HHS. The session will highlight the vital importance of early recognition and accurate diagnosis, with a focus on patient testing within the transfusion service.Chair:
Ravindra Sarode
UT Southwestern Medical Center
Dallas, Texas, United States
Speakers:
Stella T Chou, MD
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
Incorporation of Genetics into Transfusion Medicine Therapy
Susan Weiss
Atrium Health
Charlotte, North Carolina, United States
Hyperhemolysis Syndrome: A Frequently Overlooked Yet Deadly Transfusion Complication