Alternative-Donor Hematopoietic Stem Cell Transplantation with Post-Transplantation Cyclophosphamide for Nonmalignant Disorders

被引:63
作者
Klein, Orly R. [1 ]
Chen, Allen R. [1 ]
Gamper, Christopher [1 ]
Loeb, David [1 ]
Zambidis, Elias [1 ]
Llosa, Nicolas [1 ]
Huo, Jeffrey [1 ]
Dezern, Amy E. [1 ]
Steppan, Diana [1 ]
Robey, Nancy [1 ]
Holuba, Mary Jo [1 ]
Cooke, Kenneth R. [1 ]
Symons, Heather J. [1 ]
机构
[1] Johns Hopkins Univ Hosp, Pediat Blood & Marrow Transplantat Program, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21287 USA
关键词
Reduced-intensity conditioning; HLA-haploidentical; Cyclophosphamide; Immunodeficiency; Bone marrow failure syndromes; CORD BLOOD TRANSPLANTATION; BONE-MARROW-TRANSPLANTATION; VERSUS-HOST-DISEASE; CHRONIC GRANULOMATOUS-DISEASE; SINGLE-CENTER EXPERIENCE; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; PRIMARY IMMUNODEFICIENCY; PROPHYLAXIS; ALEMTUZUMAB; FLUDARABINE;
D O I
10.1016/j.bbmt.2016.02.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Allogeneic hematopoietic stem cell transplantation (HSCT) is curative for many nonmalignant pediatric disorders, including hemoglobinopathies, bone marrow failure syndromes, and immunodeficiencies. There is great success using HLA-matched related donors for these patients; however, the use of alternative donors has been associated with increased graft failure, graft-versus-host disease (GVHD), and transplant-related mortality (TRM). HSCT using alternative donors with post-transplantation cyclophosphamide (PT/Cy) for GVHD prophylaxis has been performed for hematologic malignancies with engraftment, GVHD, and TRM comparable with that seen with HLA-matched related donors. There are limited reports of HSCT in nonmalignant pediatric disorders other than hemoglobinopathies using alternative donors and PT/Cy. We transplanted 11 pediatric patients with life-threatening nonmalignant conditions using reduced-intensity conditioning, alternative donors, and PT/Cy alone or in combination with tacrolimus and mycophenolate mofetil. We observed limited GVHD, no TRM, and successful engraftment sufficient to eliminate manifestations of disease in all patients. Allogeneic HSCT using alternative donors and PT/Cy shows promise for curing nonmalignant disorders; development of prospective clinical trials to confirm these observations is warranted. (C) 2016 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:895 / 901
页数:7
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