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The European Hematology Association (EHA)
The European Hematology Association (EHA)
The
European Hematology Association
(
EHA
) is a non-governmental and not-for-profit membership organization that is guided by its mission to promote excellence in patient care, research, and education in hematology.
Wrap-Up
COMMANDS Trial in Transfusion-Dependent, Erythropoiesis-Stimulating Agent–Naïve Patients With Very Low-, Low-, or Intermediate-Risk MDS: Multilineage and Safety Results
EHA 2024 - Wrap-Up: Myelodysplastic Syndrome
At the 2024 European Hematology Association Annual Congress, researchers presented the multilineage and safety results from the COMMANDS trial of transfusion-dependent, erythropoiesis-stimulating agent–naïve patients with very low-, low-, or intermediate-risk myelodysplastic syndromes.
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Wrap-Up
Transfusion-Dependent Patients With Lower-Risk MDS Receiving Luspatercept or Epoetin Alfa: Hb and QOL
EHA 2024 - Wrap-Up: Myelodysplastic Syndrome
At the European Hematology Association 2024 Annual Conference, researchers analyzed the relationship between hemoglobin and the quality of life of transfusion-dependent patients with lower-risk myelodysplastic syndromes receiving luspatercept or epoetin alfa.
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Wrap-Up
Luspatercept in Clinical Practice: Real-World Dose Escalation and Outcomes Among Patients With Lower-Risk MDS Receiving Luspatercept in Clinical Practice
EHA 2024 - Wrap-Up: Myelodysplastic Syndrome
At the European Hematology Association 2024 Annual Conference, researchers presented the real-world dose escalation of luspatercept and its outcomes among patients with lower-risk myelodysplastic syndromes.
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Wrap-Up
Transfusion-Dependent Lower-Risk MDS: The Humanistic and Economic Burden on Patients in North America and Europe
EHA 2024 - Wrap-Up: Myelodysplastic Syndrome
At the European Hematology Association 2024 Annual Conference, researchers explored the emotional, physical, and financial burden experienced by patients with transfusion-dependent lower-risk myelodysplastic syndromes based in North America and Europe.
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Wrap-Up
Lower-Risk MDS: The Value of Early Luspatercept Use
EHA 2024 - Wrap-Up: Myelodysplastic Syndrome
Researchers presented a model to compare treatment outcomes for patients with lower-risk myelodysplastic syndromes who rely on red blood cell transfusions starting from first-line treatment initiation throughout their lifetime.
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Ixazomib, Daratumumab, and Low-Dose Dexamethasone Induction in Frail Elderly Newly Diagnosed MM Patients
EHA 2020 – Multiple Myeloma
Induction with ixazomib, daratumumab, and low-dose dexamethasone in frail elderly newly diagnosed multiple myeloma patients in the HOVON 143 study was meaningfully effective regarding ORR and PFS, but with continued toxicity concerns.
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Melflufen plus Dexamethasone in Patients with RRMM Refractory to Pomalidomide and/or an Anti-CD38 Monoclonal Antibody
EHA 2020 – Multiple Myeloma
Melflufen/dexamethasone demonstrated meaningful activity and manageable safety profile in patients with relapsed/refractory multiple myeloma who had ≥2 prior lines of therapy and were also refractory to pomalidomide and/or an anti-CD38 monoclonal antibody.
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DREAMM-2: Belantamab Mafodotin in Relapsed/Refractory Multiple Myeloma – Prior Therapy Analysis
EHA 2020 – Multiple Myeloma
In the DREAMM-2 study of belantamab mafodotin in heavily pretreated relapsed/refractory multiple myeloma patients, comparable overall response rates (~30%) were observed between patients who had 3 to 6 prior therapies and those with ≥7.
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Venetoclax vs Placebo in Combination with Bortezomib/Dexamethasone in Relapsed/Refractory Multiple Myeloma
EHA 2020 – Multiple Myeloma
Addition of venetoclax to bortezomib/dexamethasone in relapsed/refractory multiple myeloma patients (BELLINI phase 3 study) improves progression-free survival, but also results in higher mortality, with t(11;14) or
BCL2
high
gene expression patients benefiting most.
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Defining and Predicting Unsustained Complete Remission in Transplant-Eligible Multiple Myeloma Patients
EHA 2020 – Multiple Myeloma
In patients with multiple myeloma who undergo frontline optimized induction followed by ASCT, MRD assessment and clinical response time kinetics were predictive of unsustained complete remission, based on a subgroup analysis of PETHEMA/GEM2012MENOS65.
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