Journal: American Journal of Hematology
Credit: 1.0 AMA PRA Category 1 CreditTM
Release Date: February 18, 2025
Abstract
Acute myeloid leukemia is a molecularly heterogenous disease caused by the rapid expansion and impaired differentiation of malignant myeloid progenitors. Overall, outcomes remain poor, and more than half of patients develop relapsed or refractory disease after front-line therapy. Allogeneic hematopoietic stem cell transplant (HCT) remains the best chance for cure for eligible patients, and the development of novel therapies including BCL2, FLT3, IDH1/2 and menin inhibitors, which are efficacious yet generally more tolerable, have enabled better bridging to prompt HCT. Despite the early success of targeted therapies, more generalized and efficacious therapeutic approaches remain in need, and numerous targeted immunotherapeutic agents (including CAR-T, bispecific and trispecific antibody therapies) are currently under investigation.
Activity Disclosures
The publication of this supplement has been funded by Abbvie Inc.
A.S. serves as a member on the Amgen Speaker Bureau and is a consultant for Debiopharm. A.T.F. provides clinical trial support for Abbvie, Servier, and BMS, and is a consultant for the following companies: BMS, Servier, Astellas, Abbvie, PureTech, Forma, Daiichi Sankyo, Pfizer, Rigel, Autolus, Amgen, Takeda, Orum, Menarini, Remix, Ipsen, Gilead, Genentech, AstraZeneca, Syndax, Schrodinger, Prelude. The other authors declare no conflicts of interest.
This activity underwent peer review in line with standards of editorial integrity and publication ethics. Conflicts of interest have been identified and resolved in accordance with John Wiley and Sons, Inc.’s Policy on Activity Disclosure and Conflict of Interest.
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