1. Hypomethylating agent monotherapy in core binding factor acute myeloid leukemia: a French multicentric retrospective study.
- Author
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Gabellier, Ludovic, Peterlin, Pierre, Thepot, Sylvain, Hicheri, Yosr, Paul, Franciane, Gallego-Hernanz, Maria Pilar, Bertoli, Sarah, Turlure, Pascal, Pigneux, Arnaud, Guieze, Romain, Ochmann, Marlène, Malfuson, Jean-Valère, Cluzeau, Thomas, Thomas, Xavier, Tavernier, Emmanuelle, Jourdan, Eric, Bonnet, Sarah, Tudesq, Jean-Jacques, and Raffoux, Emmanuel
- Subjects
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ACUTE myeloid leukemia , *ERYTHROCYTES , *BLOOD platelets , *RETROSPECTIVE studies , *AZACITIDINE - Abstract
Very few data are available about hypomethylating agent (HMA) efficiency in core binding factor acute myeloid leukemias (CBF-AML). Our main objective was to evaluate the efficacy and safety of HMA in the specific subset of CBF-AML. Here, we report the results of a multicenter retrospective French study about efficacy of HMA monotherapy, used frontline or for R/R CBF-AML. Forty-nine patients were included, and received a median of 5 courses of azacitidine (n = 46) or decitabine (n = 3). ORR was 49% for the whole cohort with a median time to response of 112 days. After a median follow-up of 72.3 months, median OS for the total cohort was 10.6 months. In multivariate analysis, hematological relapse of CBF-AML at HMA initiation was significantly associated with a poorer OS (HR: 2.13; 95%CI: 1.04–4.36; p = 0.038). Responders had a significantly improved OS (1-year OS: 75%) compared to non-responders (1-year OS: 15.3%; p < 0.0001). Hematological improvement occurred for respectively 28%, 33% and 48% for patients who were red blood cell or platelet transfusion-dependent, or who experienced grade 3/4 neutropenia at HMA initiation. Adverse events were consistent with the known safety profile of HMA. Our study highlights that HMA is a well-tolerated therapeutic option with moderate clinical activity for R/R CBF-AML and for patients who cannot handle intensive chemotherapy. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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