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Volume 13, Issue 12, Pages 1461-1468 (December 2007)


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Peripheral Blood Grafts from Unrelated Donors Are Associated with Increased Acute and Chronic Graft-versus-Host Disease without Improved Survival

Mary Eapen1Corresponding Author Informationemail address, Brent R. Logan1, Dennis L. Confer2, Michael Haagenson1, John E. Wagner3, Daniel J. Weisdorf3, John R. Wingard4, Scott D. Rowley5, David Stroncek6, Adrian P. Gee7, Mary M. Horowitz1, Claudio Anasetti8

Received 12 April 2007; accepted 23 August 2007. published online 11 October 2007.

Abstract 

Few studies have tested the benefits of using peripheral blood stem cell (PBSC) grafts versus bone marrow (BM) grafts for unrelated donor transplantation. Yet there has been a substantial change in clinical practice, with increasing numbers of adults receiving unrelated donor PBSC grafts. We compared outcomes after 331 PBSC and 586 BM transplants in adults with leukemia and myelodysplastic syndrome (MDS) who were followed for a median of 3 years after transplantation. PBSC recipients were less likely to have chronic myelogenous leukemia (CML) and more likely to have MDS, to have poor performance scores, and to be transplanted more recently. Outcomes were analyzed using Cox regression models. Rates of grades 2-4 acute graft-versus-host disease (GVHD) (58% versus 45%, P < .001) and chronic GVHD (cGVHD) (56% versus 42%, P < .001) were significantly higher with PBSC than with BM transplants. Rates of grade II-IV aGVHD were similar with PBSC and BM transplants. The 3-year probabilities of treatment-related mortality (TRM), leukemia recurrence, leukemia-free, and overall survival (OS) were similar in the 2 groups with 3-year leukemia-free survival rates of 30% and 32% after transplantation of PBSC and BM, respectively. Unlike results after HLA-matched sibling donor PBSC transplants, we did not identify a survival advantage with PBSC grafts in patients receiving unrelated donor transplants for advanced leukemia. The higher rate of cGVHD after PBSC transplants and, consequently, more frequent late adverse events warrant extended follow up of PBSC recipients.

1 Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin

2 National Marrow Donor Program, Minneapolis, Minnesota

3 University of Minnesota, Minneapolis, Minnesota

4 Shands Hospital at the University of Florida, Gainesville, Florida

5 Hackensack University Medical Center, Hackensack, New Jersey

6 National Institutes of Health, Department of Transfusion Medicine, Bethesda, Maryland

7 Baylor College of Medicine, Houston, Texas

8 H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida

Corresponding Author InformationCorrespondence and reprint requests: Mary Eapen, M.D., Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, 8701 Watertown Plank Road, P.O. Box 26509, Milwaukee, WI 53226.

PII: S1083-8791(07)00385-0

doi:10.1016/j.bbmt.2007.08.006


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