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

Author:

Abaza Yasmin1ORCID,Winer Eric S.2,Murthy Guru Subramanian Guru3,Shallis Rory M.4,Matthews Andrew H.5ORCID,Badar Talha6ORCID,Geramita Emily M.7,Kota Vamsi K.8ORCID,Swaroop Alok1ORCID,Doukas Peter1,Bradshaw Danielle8ORCID,Helenowski Irene B.9,Liu Yingzhe9,Zhang Hui9,Im Annie7ORCID,Litzow Mark R.10ORCID,Perl Alexander E.5ORCID,Atallah Ehab3,Altman Jessica K.1

Affiliation:

1. Division of Hematology and Oncology, Leukemia Program, Robert H. Lurie Comprehensive Cancer Center Northwestern University, Feinberg School of Medicine Chicago Illinois USA

2. Department of Medical Oncology Dana‐Farber Cancer Institute Boston Massachusetts USA

3. Division of Hematology and Oncology Medical College of Wisconsin Milwaukee Wisconsin USA

4. Section of Hematology, Department of Internal Medicine Yale School of Medicine and Yale Cancer Center New Haven Connecticut USA

5. Division of Hematology‐Oncology, Perelman Center for Advanced Medicine University of Pennsylvania Philadelphia Pennsylvania USA

6. Division of Hematology and Oncology, Blood and Marrow Transplantation Program Mayo Clinic Jacksonville Florida USA

7. Division of Hematology Oncology University of Pittsburgh, UPMC Hillman Cancer Center Pittsburgh Pennsylvania USA

8. Department of Medicine, Hematology‐Oncology, Medical College of Georgia Augusta University Augusta Georgia USA

9. Division of Biostatistics, Department of Preventive Medicine Northwestern University, Feinberg School of Medicine Chicago Illinois USA

10. Division of Hematology Mayo Clinic Rochester Minnesota USA

Abstract

AbstractVenetoclax (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.

Publisher

Wiley

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