Publication

Prior rituximab correlates with less acute graft-versus-host disease and better survival in B-cell lymphoma patients who received allogeneic peripheral blood stem cell transplantation

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Last modified
  • 05/21/2025
Type of Material
Authors
    Voravit Ratanatharathorn, Wayne State UniversityBrent Logan, CIBMTRDan Wang, CIBMTRMary Horowitz, CIBMTRJoseph P. Uberti, Wayne State UniversityOlle Ringden, Karolinska University HospitalRobert Peter Gale, CelgeneHanna Khoury, Emory UniversityMukta Arora, University of MinnesotaStephen Spellman, CIBMTRCorey Cutler, Dana Farber Canc InstJoseph Antin, Dana Farber Canc InstMartin Bornhaeuser, Tech Univ DresdenGregory Hale, St Jude Childrens HospLeo Verdonck, Univ Med Ctr UtrechtMitchell Cairo, Columbia UniversityVikas Gupta, Princess Margaret HospPavletic Steven, National Institute of Health
Language
  • English
Date
  • 2009-06-01
Publisher
  • Wiley: 12 months
Publication Version
Copyright Statement
  • © 2009 Blackwell Publishing Ltd.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0007-1048
Volume
  • 145
Issue
  • 6
Start Page
  • 816
End Page
  • 824
Abstract
  • Prior therapy with rituximab might attenuate disparate histocompatibility antigen presentation by B cells, thus decreased the risk of acute graft-versus-host disease (GVHD) and improved survival. We tested this hypothesis by comparing the outcomes of 435 B-cell lymphoma patients who received allogeneic transplantation from 1999 to 2004 in the Center for International Blood and Marrow Transplant Research database: 179 subjects who received rituximab within 6 months prior to transplantation (RTX cohort) and 256 subjects who did not receive RTX within 6 months prior to transplantation (No-RTX cohort). The RTX cohort had a significantly lower incidence of treatment-related mortality (TRM) [relative risk (RR) = 0·68; 95% confidence interval (CI), 0·47-1·0; P = 0·05], lower acute grade II-IV (RR = 0·72; 95% CI, 0·53-0·97; P = 0·03) and III-IV GVHD (RR = 0·55; 95% CI, 0·34-0·91; P = 0·02). There was no difference in the risk of chronic GVHD, disease progression or relapse. Progression-free survival (PFS) (RR = 0·68; 95% CI 0·50-0·92; P = 0·01) and overall survival (OS) (RR = 0·63; 95% CI, 0·46-0·86; P = 0·004) were significantly better in the RTX cohort. Prior RTX therapy correlated with less acute GVHD, similar chronic GVHD, less TRM, better PFS and OS.
Author Notes
  • Corresponding Author: Voravit Ratanatharathorn, MD, Blood and Marrow Transplantation Program, Karmanos Cancer Institute, Wayne State University School of Medicine, 4100 John R, 4th Floor Hudson-Webber Building, Detroit, MI 48201, Phone: (313) 576-8787, Fax: (3130 576-8766, ratanath@karmanos.org.
Keywords
Research Categories
  • Health Sciences, Oncology
  • Health Sciences, Immunology

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