Multisite 11-year experience of less-intensive vs intensive therapies in acute myeloid leukemia

Mohamed L. Sorror(University of Washington Medical Center), Barry E. Storer(University of Washington), Amir T. Fathi(Harvard University), Andrew M. Brunner(Harvard University), Aaron T. Gerds(Cleveland Clinic), Mikkael A. Sekeres(Cleveland Clinic), Sudipto Mukherjee(Cleveland Clinic), Bruno C. Medeiros(Stanford University), Eunice S. Wang(Roswell Park Comprehensive Cancer Center), Pankit Vachhani(Roswell Park Comprehensive Cancer Center), Paul J. Shami(University of Utah), Esteban Peña(University of Utah), Mahmoud Elsawy(Dalhousie University), Kehinde Adekola(Northwestern University), Selina M. Luger(University of Pennsylvania), Maria R. Baer(University of Maryland, Baltimore), David A. Rizzieri(Duke Medical Center), Tanya M. Wildes(Washington University in St. Louis), Jamie Koprivnikar(Hackensack University Medical Center), Julie Smith(Wenatchee Valley Hospital & Clinics), Mitchell Garrison(Wenatchee Valley Hospital & Clinics), Kiarash Kojouri(Skagit Valley Hospital), Wendy M. Leisenring(Fred Hutch Cancer Center), Lynn Onstad(Fred Hutch Cancer Center), Jennifer E. Nyland(Penn State Milton S. Hershey Medical Center), Pamela S. Becker(University of Washington), Jeannine S. McCune(Fred Hutch Cancer Center), Stephanie J. Lee(University of Washington Medical Center), Brenda M. Sandmaier(University of Washington Medical Center), Frederick R. Appelbaum(University of Washington Medical Center), Elihu H. Estey(University of Washington)
Blood
April 28, 2021
Cited by 46Open Access
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Abstract

Less-intensive induction therapies are increasingly used in older patients with acute myeloid leukemia (AML). Using an AML composite model (AML-CM) assigning higher scores to older age, increased comorbidity burdens, and adverse cytogenetic risks, we defined 3 distinct prognostic groups and compared outcomes after less-intensive vs intensive induction therapies in a multicenter retrospective cohort (n = 1292) treated at 6 institutions from 2008 to 2012 and a prospective cohort (n = 695) treated at 13 institutions from 2013 to 2017. Prospective study included impacts of Karnofsky performance status (KPS), quality of life (QOL), and physician perception of cure. In the retrospective cohort, recipients of less-intensive therapies were older and had more comorbidities, more adverse cytogenetics, and worse KPS. Less-intensive therapies were associated with higher risks of mortality in AML-CM scores of 4 to 6, 7 to 9, and ≥10. Results were independent of allogeneic transplantation and similar in those age 70 to 79 years. In the prospective cohort, the 2 groups were similar in baseline QOL, geriatric assessment, and patient outcome preferences. Higher mortality risks were seen after less-intensive therapies. However, in models adjusted for age, physician-assigned KPS, and chance of cure, mortality risks and QOL were similar. Less-intensive therapy recipients had shorter length of hospitalization (LOH). Our study questions the survival and QOL benefits (except LOH) of less-intensive therapies in patients with AML, including those age 70 to 79 years or with high comorbidity burdens. A randomized trial in older/medically infirm patients is required to better assess the value of less-intensive and intensive therapies or their combination. This trial was registered at www.clinicaltrials.gov as #NCT01929408.


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