Long-term outcomes in FLT3-mutated acute myeloid leukemia after frontline hypomethylating agent, venetoclax and a FLT3 inhibitor
Triplet regimens with a hypomethylating agent, venetoclax and a FLT3 inhibitor yield high rates of response in newly diagnosed FLT3-mutated AML. However, the long-term outcomes and patterns of relapse with these triplet regimens are not well-established. In this retrospective analysis, 73 patients with newly diagnosed FLT3-mutated AML received a frontline FLT3 inhibitor-containing triplet regimen. The composite complete remission (CR) and CR with incomplete hematologic recovery (CRi) rate was 93%. Next-generation sequencing FLT3-ITD MRD negativity (sensitivity: 0.005%) was achieved in 60% of patients after cycle 2 and 90% after cycle 4. The estimated 3-year relapse-free survival (RFS) for FLT3-ITD-mutated and FLT3 TKD-mutated AML was 38% and 76%, respectively, and the 3-year overall survival (OS) was 45% and 76%, respectively. Neither age, NPM1 co-mutation, ELN 2022 risk, nor allogeneic stem cell transplantation in first remission significantly impacted OS. Baseline RAS pathway mutations were associated with poor long-term survival (3-year OS 22% versus 63% without RAS pathway mutation). FLT3 wild type relapses accounted for 65% of relapses, and new RAS pathway mutations were observed in 24% of relapses. Outcomes were poor after relapse (median OS of 6.1 months), particularly for those with persistently detectable FLT3 mutations. Triplet combinations of an HMA, venetoclax and a FLT3 inhibitor result in durable remission and encouraging long-term OS in older adults with newly diagnosed FLT3-mutated AML. However, better strategies to prevent FLT3 wild type relapses and to overcome RAS pathway-mediated resistance are still needed.
Authors
- Farhad Ravandi (ORCID: https://orcid.org/0000-0002-7621-377X)
- Manuel Maroun
- Keyur P. Patel (ORCID: https://orcid.org/0000-0001-5081-2427)
- Courtney D. DiNardo (ORCID: https://orcid.org/0000-0001-9003-0390)
- Tapan Mahendra Kadia (ORCID: https://orcid.org/0000-0002-9892-9832)
- Marina Konopleva (ORCID: https://orcid.org/0000-0002-9347-2212)
- Mark J. Routbort (ORCID: https://orcid.org/0000-0003-4860-261X)
- Musa Yılmaz (ORCID: https://orcid.org/0000-0002-4498-4895)
- Gautam Borthakur (ORCID: https://orcid.org/0000-0001-7679-6453)
- Elizabeth J. Shpall (ORCID: https://orcid.org/0000-0003-3947-4126)
- Sanam Loghavi (ORCID: https://orcid.org/0000-0001-8980-3202)
- Ghayas C. Issa (ORCID: https://orcid.org/0000-0002-4339-8683)
- Uday Popat (ORCID: https://orcid.org/0000-0002-7592-2224)
- Naval Daver
- Betül Oran (ORCID: https://orcid.org/0000-0003-1264-5968)
- Kunhwa Kim (ORCID: https://orcid.org/0000-0002-9709-6824)
- Omer Karrar (ORCID: https://orcid.org/0000-0001-6026-4073)
- Nicholas J. Short (ORCID: https://orcid.org/0000-0002-2983-2738)
- Hagop Kantarjian
- Joseph Jabbour
Institutions
- Albert Einstein College of Medicine (US)
- The University of Texas MD Anderson Cancer Center (US)
Publication Details
- Journal
- Haematologica
- Published
- 2025-10-02
- DOI
- https://doi.org/10.3324/haematol.2025.288553
- Citations
- 1
- Primary Topic
- Acute Myeloid Leukemia Research
- Type
- article
- Field-Weighted Citation Impact
- 1.77
Funders
- Bristol-Myers Squibb
- Pfizer
- Gilead Sciences
- Astellas Pharma
- National Institutes of Health
- Genentech
- University of Texas MD Anderson Cancer Center
- National Cancer Institute
- Daiichi Sankyo Europe