American journal of hematology · 2024
Outcomes of acute myeloid leukemia patients who responded to venetoclax and azacitidine and stopped treatment.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Garciaz Sylvain, Dumas Pierre-Yves, Bertoli Sarah, Sallman David A, Decroocq Justine, Belhabri Amine, Orvain Corentin, Aspas Requena Gaspar, Simand Celestine, Laribi Kamel, Carré Martin, Santagostino Alberto, Himberlin Chantal, Peterlin Pierre, Bonnet Sarah, Chan Onyee, Lancet Jeffrey, Komrokji Rami, Vergez François, Chapuis Nicolas, Raskovalova Tatiana, Plesa Adriana, Lhoumeau Anne-Catherine, Mineur Ariane, Hospital Marie Anne, Pigneux Arnaud, Vey Norbert, Récher Christian
Аннотация
Venetoclax-azacitidine is the standard of treatment for unfit acute myeloid leukemia patients. In the VIALE-A study, treatment was given until progression but there are no data on its optimal duration for responding patients who do not tolerate indefinite therapy. We retrospectively analyzed the outcome of patients who discontinued venetoclax or venetoclax-azacitidine due to poor tolerance. Sixty-two newly diagnosed (ND) AML patients and 22 patients with morphological relapse or refractory AML were included. In the ND cohort (n = 62), 28 patients stopped venetoclax and azacitidine and 34 patients continued azacitidine monotherapy. With a median follow-up of 23 months (IQR, 20-32), median overall survival and treatment-free survival were 44 (IQR, 16-NR) and 16 (IQR, 8-27) months, respectively. Patients who stopped both treatments and those who continued azacitidine monotherapy had the same outcomes. Negative minimal residual disease was associated with a 2-year treatment-free survival of 80%. In the RR cohort (n = 22), median overall survival and treatment-free survival were 19 (IQR, 17-31) and 10 (IQR, 5-NR) months, respectively. Prior number of venetoclax-azacitidine cycles and IDH mutations were associated with increased overall survival. The only factor significantly impacting treatment-free survival was the number of prior cycles. This study suggests that patients who discontinued treatment in remission have favorable outcomes supporting the rationale for prospective controlled trials.