Peripheral blood grafts from unrelated donors are associated with increased acute and chronic graft-versus-host disease without improved survival

被引:145
作者
Eapen, Mary
Logan, Brent R.
Confer, Dennis L.
Haagenson, Michael
Wagner, John E.
Weisdorf, Daniel J.
Wingard, John R.
Rowley, Scott D.
Stroncek, David
Gee, Adrian P.
Horowitz, Mary M.
Anasetti, Claudio
机构
[1] Med Coll Wisconsin, Ctr Int Blood & Marrow Transplant Res, Milwaukee, WI 53226 USA
[2] Natl Marrow Donor Program, Minneapolis, MN USA
[3] Univ Minnesota, Minneapolis, MN USA
[4] Univ Florida, Shands Hosp, Gainesville, FL USA
[5] Hackensack Univ Med Ctr, Hackensack, NJ USA
[6] NIH, Dept Transfus Med, Bethesda, MD 20892 USA
[7] Baylor Coll Med, Houston, TX 77030 USA
[8] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL 33612 USA
关键词
peripheral blood graft; graft-versus-host disease; unrelated donor transplant;
D O I
10.1016/j.bbmt.2007.08.006
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
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 B-LA-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. (c) 2007 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:1461 / 1468
页数:8
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