Risk factors for acute GVHD and survival after hematopoietic cell transplantation

Madan Jagasia(Vanderbilt University Medical Center), Mukta Arora(University of Minnesota), Mary E.D. Flowers(University of Washington), Nelson J. Chao(Duke Medical Center), Philip L. McCarthy(Roswell Park Comprehensive Cancer Center), Corey Cutler(Dana-Farber Cancer Institute), Álvaro Urbano-Ispizúa(Hospital Clínic de Barcelona), Steven Z. Pavletic(National Institutes of Health), Michael Haagenson(National Marrow Donor Program), Mei-Jie Zhang(Medical College of Wisconsin), Joseph H. Antin(Dana-Farber Cancer Institute), Brian J. Bolwell(Cleveland Clinic), Christopher Bredeson(University of Ottawa), Jean‐Yves Cahn(Centre Hospitalier Universitaire de Grenoble), Mitchell S. Cairo(New York Medical College), Robert Peter Gale, Vikas Gupta(Princess Margaret Hospital), Stephanie J. Lee(University of Washington), Mark R. Litzow(Mayo Clinic in Arizona), Daniel J. Weisdorf(University of Minnesota), Mary M. Horowitz(Medical College of Wisconsin), Theresa Hahn(Roswell Park Comprehensive Cancer Center)
Blood
October 19, 2011
Cited by 695

Abstract

Abstract Risk factors for acute GVHD (AGVHD), overall survival, and transplant-related mortality were evaluated in adults receiving allogeneic hematopoietic cell transplants (1999-2005) from HLA-identical sibling donors (SDs; n = 3191) or unrelated donors (URDs; n = 2370) and reported to the Center for International Blood and Marrow Transplant Research, Minneapolis, MN. To understand the impact of transplant regimen on AGVHD risk, 6 treatment categories were evaluated: (1) myeloablative conditioning (MA) with total body irradiation (TBI) + PBSCs, (2) MA + TBI + BM, (3) MA + nonTBI + PBSCs, (4) MA + nonTBI + BM, (5) reduced intensity conditioning (RIC) + PBSCs, and (6) RIC + BM. The cumulative incidences of grades B-D AGVHD were 39% (95% confidence interval [CI], 37%-41%) in the SD cohort and 59% (95% CI, 57%-61%) in the URD cohort. Patients receiving SD transplants with MA + nonTBI + BM and RIC + PBSCs had significantly lower risks of grades B-D AGVHD than patients in other treatment categories. Those receiving URD transplants with MA + TBI + BM, MA + nonTBI + BM, RIC + BM, or RIC + PBSCs had lower risks of grades B-D AGVHD than those in other treatment categories. The 5-year probabilities of survival were 46% (95% CI, 44%-49%) with SD transplants and 33% (95% CI, 31%-35%) with URD transplants. Conditioning intensity, TBI and graft source have a combined effect on risk of AGVHD that must be considered in deciding on a treatment strategy for individual patients.


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