
Faculty, Staff and Student Publications
Publication Date
4-1-2025
Journal
Leukemia
Abstract
Intensive chemotherapy remains the standard for newly diagnosed (ND) acute myeloid leukemia (AML); however, relapse risk remains high. Additionally, most patients with relapsed/refractory (RR) AML have poor outcomes. We report the long-term experience of 138 patients, 77 ND and 61 RR, treated with FLAG-IDA in combination with venetoclax. In the ND cohort, the overall response rate (ORR) was 97%, with a composite complete remission (CRc) rate of 95% and undetectable measurable residual disease (MRD) status by flow cytometry in 90%. The 3-year OS and EFS rates were 66 and 64%, respectively. Outcomes were similar across European LeukemiaNet (ELN) 2022 risk groups. Sixty-four percent transitioned to allogeneic hematopoietic stem cell transplantation (allo-SCT) in CR1. In the RR cohort, the ORR was 67%; CRc rate 41% and flow negative MRD rate 74%; 57% transitioned to allo-SCT. The patients with RR AML in first salvage with wild-type TP53 status had particularly favorable outcomes, with an ORR of 79%, CRc rate of 74% (76% MRD undetectable) and 3-year OS rate of 51%. Infectious and hematologic adverse events were common, with low 30- and 60-day mortality similar to other intensive chemotherapy regimens. FLAG-IDA + VEN is effective for remission induction in both ND and RR AML.ClinicalTrials.gov Identifier: NCT03214562.
Keywords
Humans, Leukemia, Myeloid, Acute, Female, Male, Bridged Bicyclo Compounds, Heterocyclic, Middle Aged, Antineoplastic Combined Chemotherapy Protocols, Sulfonamides, Aged, Adult, Young Adult, Neoplasm Recurrence, Local, Hematopoietic Stem Cell Transplantation, Neoplasm, Residual, Cytarabine, Idarubicin, Remission Induction, Survival Rate, Consolidation Chemotherapy, Drug Resistance, Neoplasm, Follow-Up Studies, Induction Chemotherapy, Prognosis, Adolescent
DOI
10.1038/s41375-025-02531-8
PMID
40000842
PMCID
PMC11978487
PubMedCentral® Posted Date
4-9-2025
PubMedCentral® Full Text Version
Author MSS
Published Open-Access
yes
Included in
Bioinformatics Commons, Biomedical Informatics Commons, Genetic Phenomena Commons, Hematology Commons, Hemic and Lymphatic Diseases Commons, Medical Genetics Commons, Oncology Commons