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Article Abstract

Introduction: This phase 2 study evaluated magrolimab+venetoclax (VEN)+azacitidine (AZA) in untreated, unfit acute myeloid leukaemia (AML) and magrolimab+mitoxantrone+etoposide+cytarabine in relapsed/refractory (R/R) AML.

Methods: Endpoints included complete remission rate (CRR), overall response rate (ORR), overall survival (OS) and safety.

Results: Eighteen and 36 patients were enrolled into the unfit and R/R AML arms, respectively. CRR was 38.9% and 25.0%, ORR was 66.7% and 38.9%, and median OS was 15.3 and 10.5 months in the unfit AML and R/R AML arms, respectively. No dose-limiting toxicities or magrolimab-related deaths occurred.

Conclusion: Magrolimab was safely combined with existing AML therapies with no new safety signals.

Clinical Trial Registration: This trail was registered at www.clinicaltrials.gov as NCT04778410.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12073901PMC
http://dx.doi.org/10.1002/jha2.70051DOI Listing

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