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Clinical outcomes of hypomethylating agents plus Venetoclax as frontline treatment in patients 75 years and older with acute myeloid leukemia: Real-world data from eight US academic centers.
Abaza, Yasmin; Winer, Eric S; Murthy, Guru Subramanian Guru; Shallis, Rory M; Matthews, Andrew H; Badar, Talha; Geramita, Emily M; Kota, Vamsi K; Swaroop, Alok; Doukas, Peter; Bradshaw, Danielle; Helenowski, Irene B; Liu, Yingzhe; Zhang, Hui; Im, Annie; Litzow, Mark R; Perl, Alexander E; Atallah, Ehab; Altman, Jessica K.
Afiliación
  • Abaza Y; Division of Hematology and Oncology, Leukemia Program, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
  • Winer ES; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
  • Murthy GSG; Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Shallis RM; Section of Hematology, Department of Internal Medicine, Yale School of Medicine and Yale Cancer Center, New Haven, Connecticut, USA.
  • Matthews AH; Division of Hematology-Oncology, Perelman Center for Advanced Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Badar T; Division of Hematology and Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, Florida, USA.
  • Geramita EM; Division of Hematology Oncology, University of Pittsburgh, UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.
  • Kota VK; Department of Medicine, Hematology-Oncology, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
  • Swaroop A; Division of Hematology and Oncology, Leukemia Program, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
  • Doukas P; Division of Hematology and Oncology, Leukemia Program, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
  • Bradshaw D; Department of Medicine, Hematology-Oncology, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
  • Helenowski IB; Division of Biostatistics, Department of Preventive Medicine, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
  • Liu Y; Division of Biostatistics, Department of Preventive Medicine, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
  • Zhang H; Division of Biostatistics, Department of Preventive Medicine, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
  • Im A; Division of Hematology Oncology, University of Pittsburgh, UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.
  • Litzow MR; Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
  • Perl AE; Division of Hematology-Oncology, Perelman Center for Advanced Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Atallah E; Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Altman JK; Division of Hematology and Oncology, Leukemia Program, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Am J Hematol ; 99(4): 606-614, 2024 04.
Article en En | MEDLINE | ID: mdl-38342997
ABSTRACT
Venetoclax (VEN) combined with hypomethylating agents (HMAs) is the standard of care for the treatment of patients with newly diagnosed acute myeloid leukemia (AML) unfit for intensive chemotherapy. To date, real-world data published on HMAs plus VEN have been either single-center studies or using community-based electronic databases with limited details on mutational landscape, tolerability, and treatment patterns in elderly patients. Therefore, we conducted a multicenter retrospective study to assess the real-world experience of 204 elderly patients (≥75 years) with newly diagnosed AML treated with HMAs plus VEN from eight academic centers in the United States. Overall, 64 patients achieved complete remission (CR; 38%) and 43 CR with incomplete count recovery (CRi; 26%) for a CR/CRi rate of 64%, with a median duration of response of 14.2 months (95% CI 9.43, 22.1). Among responders, 63 patients relapsed (59%) with median overall survival (OS) after relapse of 3.4 months (95% CI, 2.4, 6.7). Median OS for the entire population was 9.5 months (95% CI, 7.85-13.5), with OS significantly worse among patients with TP53-mutated AML (2.5 months) and improved in patients harboring NPM1, IDH1, and IDH2 mutations (13.5, 18.3, and 21.1 months, respectively). The 30-day and 60-day mortality rates were 9% and 19%, respectively. In conclusion, HMAs plus VEN yielded high response rates in elderly patients with newly diagnosed AML. The median OS was inferior to that reported in the VIALE-A trial. Outcomes are dismal after failure of HMAs plus VEN, representing an area of urgent unmet clinical need.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Compuestos Bicíclicos Heterocíclicos con Puentes Tipo de estudio: Clinical_trials / Observational_studies Límite: Aged / Humans Idioma: En Revista: Am J Hematol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Compuestos Bicíclicos Heterocíclicos con Puentes Tipo de estudio: Clinical_trials / Observational_studies Límite: Aged / Humans Idioma: En Revista: Am J Hematol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos