Venetoclax and azacitidine for younger acute myeloid leukemia patients independent of fitness for intensive chemotherapy
Venetoclax (ven)+azacitidine (aza) is the standard of care for newly-diagnosed acute myeloid leukemia (AML) patients who are not candidates for intensive chemotherapy (IC). Because prognostic factors for ven/aza and IC differ, an AML patient fit for IC may derive more benefit from ven/aza. We therefore designed a trial for younger, newly-diagnosed AML patients with non-favorable risk disease to receive ven/aza regardless of "fitness" for IC. We aimed to understand toxicity and efficacy in this population, and retrospectively compared outcomes to matched IC patients. Newly-diagnosed non-favorable risk patients ≤60 were enrolled and received ven, dose escalated to 600mg/dailyx28 days, with aza 75mg/m2x7 days on a 28-day cycle. Subjects were encouraged to move expeditiously to allogeneic stem cell transplant (ASCT) in first remission. Thirty-six subjects enrolled. Median age was 49 (22-59). Grade ≥3 neutropenia(42%), anemia(33%), thrombocytopenia(53%) and febrile neutropenia(36%) were common. The overall response rate (ORR) was 25/36 (69%) with 19 (53%) complete remissions; 68% of responders achieved MRD-negativity. Most subjects (53%) bridged to ASCT, and the majority of non-responders were successfully salvaged with IC. The median progressionfree- survival (PFS) and overall survival (OS) have not been reached (median follow-up 2.9 years). Compared to IC matched controls, the ORR, ASCT rate and PFS were significantly improved (69% vs 44% [p=0.0495], 53% vs 28% [p-0.0290] and not reached vs 60.8 months [p=0.007]). Hospital days, transfusions and infectious complications were significantly reduced for ven/aza subjects. Ven/aza is feasible for newly-diagnosed, younger, non-favorable risk AML patients, and appears at least as effective as IC.
Authors
- Ellen Madarang (ORCID: https://orcid.org/0000-0002-9951-9958)
- Justin M. Watts (ORCID: https://orcid.org/0000-0001-5213-5482)
- Sangeetha Venugopal (ORCID: https://orcid.org/0000-0002-8641-6415)
- Alessia Zoso (ORCID: https://orcid.org/0000-0002-6834-4497)
- Nicholas Willard (ORCID: https://orcid.org/0000-0003-4912-201X)
- Jonathan A. Gutman (ORCID: https://orcid.org/0000-0002-1470-0716)
- Dara L. Aisner (ORCID: https://orcid.org/0000-0001-5203-5932)
- Namrata S. Chandhok (ORCID: https://orcid.org/0000-0002-7464-4509)
- C. Estelle Smith (ORCID: https://orcid.org/0000-0002-4981-7105)
- Terrence Bradley
- Ayele Belachew
- Christine M. McMahon (ORCID: https://orcid.org/0000-0001-9745-9595)
- Jeffrey Schowinsky (ORCID: https://orcid.org/0009-0009-8653-3820)
- Connor Sohalski
- Mary Haag
- Mary Berg (ORCID: https://orcid.org/0000-0002-4961-245X)
- J. Richard Taylor
- Jessie Dell-Martin
- Zenggang Pan
- Payton Hart
- Maria L. Amaya
- Craig Jordan
- Mikkael A. Sekeres
- Daniel A. Pollyea
- Diana Abbott
- Marc Schwartz
- Andrew Kent
- Jinjing Zhang
Institutions
- University of Miami (US)
- Children's Hospital Colorado (US)
- Sylvester Comprehensive Cancer Center (US)
- University of Colorado Anschutz Medical Campus (US)
- University of Colorado Denver (US)
Publication Details
- Journal
- Haematologica
- Published
- 2026-02-26
- DOI
- https://doi.org/10.3324/haematol.2025.300374
- Primary Topic
- Acute Myeloid Leukemia Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Leukemia and Lymphoma Society