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Intensive Induction Chemotherapy versus Hypomethylating Agents in Combination with Venetoclax in NPM1-mutant AML.
Bewersdorf, Jan Philipp; Shimony, Shai; Shallis, Rory M; Liu, Yiwen; Berton, Guillaume; Schaefer, Eva Johanna; Zeidan, Amer M; Goldberg, Aaron D; Stein, Eytan M; Marcucci, Guido; Bystrom, Rebecca; Lindsley, R Coleman; Chen, Evan C; Ramos Perez, Jorge Miguel; Stein, Anthony S; Pullarkat, Vinod A; Aldoss, Ibrahim; DeAngelo, Daniel J; Neuberg, Donna S; Stone, Richard M; Garciaz, Sylvain; Ball, Brian J; Stahl, Maximilian.
Afiliação
  • Bewersdorf JP; Memorial Sloan Kettering Cancer Center, New York, New York, United States.
  • Shimony S; Dana-Farber Cancer Institute, Boston, Massachusetts, United States.
  • Shallis RM; Yale University School of Medicine, New Haven, Connecticut, United States.
  • Liu Y; Dana Farber Cancer Institute, Boston, Massachusetts, United States.
  • Berton G; Department of Hematology, Institut Paoli-Calmettes, INSERM UMR 1068, CNRS UMR725, CNRS, Aix-Marseille University, Marseille, France, Marseille, France.
  • Schaefer EJ; Dana-Farber Cancer Institute, Boston, Massachusetts, United States.
  • Zeidan AM; Yale University, New Haven, Connecticut, United States.
  • Goldberg AD; Memorial Sloan Kettering Cancer Center, New York, New York, United States.
  • Stein EM; Memorial Sloan Kettering Cancer Center, New York, New York, United States.
  • Marcucci G; Hematologic Malignancies Translational Science, Gehr Family Center for Leukemia Research, City of Hope Medical Center and Beckman Research Institute, Duarte, California, United States.
  • Bystrom R; Dana-Farber Cancer Institute, Boston, Massachusetts, United States.
  • Lindsley RC; Dana-Farber Cancer Institute, Boston, Massachusetts, United States.
  • Chen EC; Dana-Farber Cancer Institute, Boston, Massachusetts, United States.
  • Ramos Perez JM; City of Hope Medical Center, Duarte, CA, United States, United States.
  • Stein AS; City of Hope National Medical Center, Duarte, California, United States.
  • Pullarkat VA; City of Hope Medical Center, Duarte, California, United States.
  • Aldoss I; City of Hope National Medical Center, Duarte, California, United States.
  • DeAngelo DJ; Dana-Farber Cancer Institute, Boston, Massachusetts, United States.
  • Neuberg DS; Dana-Farber Cancer Institute, Boston, Massachusetts, United States.
  • Stone RM; Dana-Farber Cancer Institute, Boston, Massachusetts, United States.
  • Garciaz S; Département d'hématologie, Institut Paoli-Calmettes, Université d'Aix-Marseille, INSERM U1068, CNRS, Marseille, France, MARSEILLE, France.
  • Ball BJ; City of Hope National Medical Center, Duarte, California, United States.
  • Stahl M; Dana-Farber Cancer Institute, Boston, Massachusetts, United States.
Blood Adv ; 2024 Jun 28.
Article em En | MEDLINE | ID: mdl-38941537
ABSTRACT
While intensive induction chemotherapy (IC) remains the standard of care for younger patients with acute myeloid leukemia (AML), data from older patients shows that hypomethylating agents + venetoclax (HMA/VEN) can lead to durable remissions among patients with NPM1 mutations. Whether IC or HMA/VEN is superior in patients ≥60 years-old with NPM1-mutant AML is unknown. To compare IC and HMA/VEN, we performed an international, multicenter retrospective cohort study of patients with newly diagnosed, NPM1-mutant AML.We included 221 patients (147 IC, 74 HMA/VEN) with previously untreated NPM1-mutant AML. Composite complete remission (cCR; defined as CR + CR with incomplete count recovery [CRi]) rate was similar for IC and HMA/VEN (cCR 85% vs. 74%; p=0.067). While OS was favorable with IC in unselected patients compared to HMA/VEN (24-month OS 59% [95% CI 52-69%] vs. 38% [95% CI 27-55%]; p=0.013), it was not statistically different among patients 60-75 years-old (60% [95% CI 52-70%] vs. 44% [95% CI 29-66%]; p=0.069) and patients who received an allogeneic stem cell transplant (70% [95% CI 58-85%] vs. 66% [95% CI 44-100%]; p=0.56). Subgroup analyses suggested that patients with normal cytogenetics (24-month OS with IC 65% [95% 56-74%] vs. 40% [95% CI 26-60%] with HMA/VEN; p=0.009) and without FLT3-ITD mutations might benefit from IC compared with HMA/VEN (24-month OS 68% [95% CI 59-79%] vs. 43% [95% CI 29-63%]; p=0.008). In multivariable analysis, OS was not statistically different for patients treated with IC and HMA/VEN (hazard ratio for death HMA/VEN vs. IC 0.71; 95% CI 0.40-1.27; p=0.25).

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article