Publication

Long-Term Sustained Disease Control in Patients With Mantle Cell Lymphoma With or Without Active Disease After Treatment With Allogeneic Hematopoietic Cell Transplantation After Nonmyeloablative Conditioning

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Last modified
  • 02/25/2025
Type of Material
Authors
    Jennifer E. Vaughn, Fred Hutchinson Cancer Research CenterMohamed L. Sorror, Fred Hutchinson Cancer Research CenterBarry E. Storer, Fred Hutchinson Cancer Research CenterThomas R. Chauncey, Fred Hutchinson Cancer Research CenterMichael A. Pulsipher, Primary Children's HospitalRichard T. Maziarz, OHSU Knight Cancer InstituteMichael B. Maris, Colorado Blood Cancer InstituteParameswaran Hari, Medical College of WisconsinGinna G. Laport, Stanford UniversityGeorg N. Franke, University of LeipzigEdward D. Agura, Baylor UniversityAmelia Langston, Emory UniversityAndrew Rezvani, Stanford UniversityRainer Storb, Fred Hutchinson Cancer Research CenterBrenda M. Sandmaier, Fred Hutchinson Cancer Research CenterDavid G. Maloney, Fred Hutchinson Cancer Research Center
Language
  • English
Date
  • 2015-07-24
Publisher
  • Wiley-Blackwell
Publication Version
Copyright Statement
  • © 2015 American Cancer Society.
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 121
Issue
  • 20
Start Page
  • 3709
End Page
  • 3716
Grant/Funding Information
  • This study was supported by grants CA018029, CA15704, CA078902, HL088021 and 5T32HL007093-38 from the National Heart Lung Blood Institute, the National Institutes of Health.
  • M.L.S. is also supported by a Research Scholar Grant No. RSG-13- 084-01-CPHPS from the American Cancer Society; and by Patient-Centered Outcome Research Institute Contract No. CE-1304-7451.
Abstract
  • BACKGROUND Previously, early results were reported for allogeneic hematopoietic cell transplantation (HCT) after nonmyeloablative conditioning with 2 Gy of total body irradiation with or without fludarabine and/or rituximab in 33 patients with mantle cell lymphoma (MCL). METHODS This study examined the outcomes of 70 patients with MCL and included extended follow-up (median, 10 years) for the 33 initial patients. Grafts were obtained from human leukocyte antigen (HLA)-matched, related donors (47%), unrelated donors (41%), and HLA antigen-mismatched donors (11%). RESULTS The 5-year incidence of nonrelapse mortality was 28%. The relapse rate was 26%. The 5-year rates of overall survival (OS) and progression-free survival (PFS) were 55% and 46%, respectively. The 10-year rates of OS and PFS were 44% and 41%, respectively. Eighty percent of surviving patients were off immunosuppression at the last follow-up. The presence of relapsed or refractory disease at the time of HCT predicted a higher rate of relapse (hazard ratio [HR], 2.94; P =.05). Despite this, OS rates at 5 (51% vs 58%) and 10 years (43% vs 45%) were comparable between those with relapsed/refractory disease and those undergoing transplantation with partial or complete remission. A high-risk cytomegalovirus (CMV) status was the only independent predictor of worse OS (HR, 2.32; P =.02). A high-risk CMV status and a low CD3 dose predicted PFS (HR, 2.22; P =.03). CONCLUSIONS Nonmyeloablative allogeneic HCT provides a long-term survival benefit for patients with relapsed MCL, including those with refractory disease or multiple relapses.
Author Notes
  • Correspondence to: Mohamed L. Sorror, M.D., Clinical Research Division (D1-100), Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Seattle, WA 98109-1024, Telephone: 206-667-2765, Fax: 206-667-6124, Email:msorror@fredhutch.org
Keywords
Research Categories
  • Health Sciences, Oncology
  • Health Sciences, General
  • Biology, Cell

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