Evolving trends and outcomes in older patients with acute myeloid leukemia including allogeneic stem cell transplantation

Author:

Bazinet Alexandre1ORCID,Kantarjian Hagop1ORCID,Arani Naszrin2,Popat Uday3,Bataller Alex1ORCID,Sasaki Koji1ORCID,DiNardo Courtney D.1ORCID,Daver Naval1ORCID,Yilmaz Musa1ORCID,Abbas Hussein A.14ORCID,Short Nicholas J.1ORCID,Issa Ghayas1ORCID,Jabbour Elias1ORCID,Pierce Sherry A.1,Chen Julianne3,Garcia Ricky3,Konopleva Marina1,Garcia‐Manero Guillermo1ORCID,Alousi Amin3,Shpall Elizabeth J.3,Champlin Richard E.3,Borthakur Gautam1ORCID,Ravandi Farhad1ORCID,Kadia Tapan1ORCID

Affiliation:

1. Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA

2. Department of Medicine Baylor College of Medicine Houston Texas USA

3. Department of Stem Cell Transplantation and Cellular Therapy The University of Texas MD Anderson Cancer Center Houston Texas USA

4. Department of Genomic Medicine The University of Texas MD Anderson Cancer Center Houston Texas USA

Abstract

AbstractOutcomes in older patients with acute myeloid leukemia (AML) have historically been poor. Given advances in low‐intensity therapy (LIT) and stem cell transplantation (SCT), we performed a retrospective single‐center study to evaluate the contemporary outcomes of this population. We reviewed all patients ≥60 years with newly diagnosed AML between 2012 and 2021 and analyzed treatment and SCT‐related trends and outcomes. We identified 1073 patients with a median age of 71 years. Adverse clinical and cytomolecular findings were frequent within this cohort. In total, 16% of patients were treated with intensive chemotherapy, 51% with LIT alone, and 32% with LIT plus venetoclax. The composite complete remission rate with LIT plus venetoclax was 72%, which was higher than with LIT alone (48%, p < .0001) and comparable to intensive chemotherapy (74%, p = .6). The median overall survival (OS) with intensive chemotherapy, LIT, and LIT plus venetoclax was 20.1, 8.9, and 12.1 months, respectively. 18% of patients received SCT. SCT rates were 37%, 10%, and 22% in patients treated with intensive chemotherapy, LIT, and LIT plus venetoclax, respectively. The 2‐year OS, relapse‐free survival (RFS), cumulative incidence (CI) of relapse, and CI of treatment‐related mortality with frontline SCT (n = 139) were 59%, 52%, 27%, and 22%, respectively. By landmark analysis, patients undergoing frontline SCT had superior OS (median 39.6 vs. 21.4 months, p < .0001) and RFS (30.9 vs. 12.1 months, p < .0001) compared with responding patients who did not. Outcomes in older patients with AML are improving with more effective LIT. Measures should be pursued to increase access to SCT in older patients.

Publisher

Wiley

Subject

Hematology

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