Risk factors for acute GVHD and survival after hematopoietic cell transplantation

Author:

Jagasia Madan1,Arora Mukta2,Flowers Mary E. D.3,Chao Nelson J.4,McCarthy Philip L.5,Cutler Corey S.6,Urbano-Ispizua Alvaro7,Pavletic Steven Z.8,Haagenson Michael D.9,Zhang Mei-Jie10,Antin Joseph H.6,Bolwell Brian J.11,Bredeson Christopher12,Cahn Jean-Yves13,Cairo Mitchell14,Gale Robert Peter15,Gupta Vikas16,Lee Stephanie J.3,Litzow Mark17,Weisdorf Daniel J.2,Horowitz Mary M.10,Hahn Theresa5

Affiliation:

1. Vanderbilt University Medical Center, Nashville, TN;

2. University of Minnesota, Minneapolis, MN;

3. Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA;

4. Duke University Medical Center, Durham, NC;

5. Roswell Park Cancer Institute, Buffalo, NY;

6. Dana-Farber Cancer Institute, Boston, MA;

7. Hospital Clinico, Barcelona, Spain;

8. Experimental Transplantation and Immunology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD;

9. Center for International Blood and Marrow Transplant Research, Minneapolis, MN;

10. Medical College of Wisconsin, Center for International Blood and Marrow Transplant Research, Milwaukee, WI;

11. Cleveland Clinic Foundation, Cleveland, OH;

12. The Ottawa Hospital Blood and Marrow Transplant Program, University of Ottawa, Ottawa, ON;

13. Hospital A. Michallon, Centre de Hospitalier de Grenoble, Grenoble, France;

14. New York Medical College, Columbia University Medical Center, New York, NY;

15. Center for Advanced Studies in Leukemia, Los Angeles, CA;

16. Princess Margaret Hospital, Toronto, ON; and

17. Mayo Clinic, Rochester, MN

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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference44 articles.

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