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Cytogenetic Risk Determines Outcomes After Allogeneic Transplantation in Older Patients With Acute Myeloid Leukemia in Their Second Complete Remission: A Center for International Blood and Marrow Transplant Research Cohort Analysis

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Last modified
  • 05/15/2025
Type of Material
Authors
    Fotios V. Michelis, Princes Margaret Cancer CenterVikas Gupta, Emory UniversityMei-Jie Zhang, Medical College of WisconsinHai-Lin Wang, Medical College of WisconsinMahmoud Aljurf, Medical College of WisconsinUlrike Bacher, University Medicine GoettingenAmer Beitinjaneh, University of MiamiYi-Bin Chen, Massachusetts General HospitalZachariah DeFilipp, Emory University HospitalRobert Peter Gale, Imperial College LondonPartow Kebriaei, University Texas MD Anderson Cancer CenterMohamed Kharfan-Dabaja, H. Lee Moffitt Cancer Center & Research InstituteHillard M. Lazarus, Seidman Cancer CenterTaiga Nishihori, H. Lee Moffitt Cancer Center & Research InstituteRichard F. Olsson, Karolinska InstitutetBetul Oran, Imperial College LondonArmin Rashidi, Washington UniversityDavid A. Rizzieri, Duke UniversityMartin S. Tallman, Memorial Sloan Kettering Cancer CenterMarcos de Lima, Seidman Cancer CenterH Jean Khoury, Emory UniversityBrenda M. Sandmaier, University of WashingtonDaniel Weisdorf, University MinnesotaWael Saber, Medical College of Wisconsin
Language
  • English
Date
  • 2017-06-01
Publisher
  • Wiley: 12 months
Publication Version
Copyright Statement
  • © 2017 American Cancer Society
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0008-543X
Volume
  • 123
Issue
  • 11
Start Page
  • 2035
End Page
  • 2042
Grant/Funding Information
  • The CIBMTR is supported by Public Health Service Grant/Cooperative Agreement 5U24-CA076518 from the National Cancer Institute (NCI), the National Heart, Lung and Blood Institute (NHLBI) and the National Institute of Allergy and Infectious Diseases (NIAID); a Grant/Cooperative Agreement 5U10HL069294 from NHLBI and NCI; a contract HHSH250201200016C with Health Resources and Services Administration (HRSA/DHHS); two Grants N00014-15-1-0848 and N00014-16-1-2020 from the Office of Naval Research; and grants from Alexion; *Amgen, Inc.; Anonymous donation to the Medical College of Wisconsin; Astellas Pharma US; AstraZeneca; Be the Match Foundation; *Bluebird Bio, Inc.; *Bristol Myers Squibb Oncology; *Celgene Corporation; Cellular Dynamics International, Inc.; *Chimerix, Inc.; Fred Hutchinson Cancer Research Center; Gamida Cell Ltd.; Genentech, Inc.; Genzyme Corporation; *Gilead Sciences, Inc.; Health Research, Inc. Roswell Park Cancer Institute; HistoGenetics, Inc.; Incyte Corporation; Janssen Scientific Affairs, LLC; *Jazz Pharmaceuticals, Inc.; Jeff Gordon Children's Foundation; The Leukemia & Lymphoma Society; Medac, GmbH; MedImmune; The Medical College of Wisconsin; *Merck & Co, Inc.; Mesoblast; MesoScale Diagnostics, Inc.; *Miltenyi Biotec, Inc.; National Marrow Donor Program; Neovii Biotech NA, Inc.; Novartis Pharmaceuticals Corporation; Onyx Pharmaceuticals; Optum Healthcare Solutions, Inc.; Otsuka America Pharmaceutical, Inc.; Otsuka Pharmaceutical Co, Ltd. – Japan; PCORI; Perkin Elmer, Inc.; Pfizer, Inc; *Sanofi US; *Seattle Genetics; *Spectrum Pharmaceuticals, Inc.; St. Baldrick's Foundation; *Sunesis Pharmaceuticals, Inc.; Swedish Orphan Biovitrum, Inc.; Takeda Oncology; Telomere Diagnostics, Inc.; University of Minnesota; and *Wellpoint, Inc.
Abstract
  • BACKGROUND: Allogeneic hematopoietic cell transplantation (HCT) offers curative potential to a number of older patients with acute myeloid leukemia (AML) in their first complete remission. However, there are limited data in the literature concerning post-HCT outcomes for older patients in their second complete remission (CR2). METHODS: The purpose of the current study was to retrospectively investigate within the Center for International Blood and Marrow Transplant Research database parameters influencing posttransplant outcomes for patients 60 years of age or older undergoing HCT for AML in CR2. RESULTS: In total, 196 patients from 78 centers were identified; the median age was 64 years (range, 60-78 years). Seventy-one percent had a Karnofsky performance status ≥ 90 at the time of HCT. Reduced-intensity conditioning regimens were used in 159 patients (81%). A univariate analysis demonstrated a 3-year overall survival (OS) rate of 42% (95% confidence interval [CI], 35%-49%), a leukemia-free survival rate of 37% (95% CI, 30%-44%), a cumulative incidence of nonrelapse mortality of 25% (95% CI, 19%-32%), and a cumulative incidence of relapse (CIR) of 38% (95% CI, 31%-45%). A multivariate analysis demonstrated that cytogenetic risk was the only independent risk factor for OS (P =.023) with a hazard ratio (HR) of 1.14 (95% CI, 0.59-2.19) for intermediate-risk cytogenetics and an HR of 2.32 (95% CI, 1.05-5.14) for unfavorable-risk cytogenetics. For CIR, cytogenetic risk was also the only independent prognostic factor (P =.01) with an HR of 1.10 (95% CI, 0.47-2.56) for intermediate-risk cytogenetics and an HR of 2.98 (95% CI, 1.11-8.00) for unfavorable-risk cytogenetics. CONCLUSIONS: Allogeneic HCT is a curative treatment option for older patients with AML in CR2, particularly for those with favorable or intermediate cytogenetic risk. Cancer 2017;123:2035–2042.
Author Notes
  • Corresponding Author Dr. Fotios V. Michelis MD, PhD, Allogeneic Blood and Marrow Transplant Program, Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, 610 University Avenue, Toronto, Ontario, Canada M5G2M9, Tel: +1(416) 946-4501 ext 4013, Fotios.Michelis@uhn.ca
Keywords
Research Categories
  • Health Sciences, Oncology
  • Health Sciences, General

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