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单倍体相合或非血缘供者造血干细胞移植治疗重型再生障碍性贫血的临床分析

[Clinical analysis of haploidentical or unrelated donor hematopoietic stem cell transplantation for patients with severe aplastic anemia].

作者信息

Chen Hui-Ren, Lou Jing-Xing, Zhang Yuan, Liu Xiao-Dong, Yang Kai, Chen Peng, Liu Bing, He Xue-Peng, Guo Zhi, Liu Dan

机构信息

Department of Hematology, General Hospital of Beijing Millitary Area, Beijing, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2012 Aug;20(4):959-64.

Abstract

Objective of this study was to evaluate the efficacy and safety of haploidentical or unrelated donor hematopoietic stem cell transplantation (HSCT) for patients with severe aplastic anemia (SAA). Twenty patients with SAA received allogeneic HSCT from haploidentical or unrelated donors (14 from haploidentical donors and 6 from unrelated donors) from November 2005 to May 2011. Conditioning regimen consisted of fludarabine (FLU), cyclophosphamide (Cy) and anti-thymocyte immunoglobulin (ATG). The patients were administrated with G-CSF-primed bone marrow and mobilized peripheral blood as grafts from haploidentical donor or only mobilized peripheral blood from the unrelated donor. The results showed that the median time of neutrophil and platelet engraftment were 14 (11 - 20) d and 17 (13 - 31) d respectively. All patients who achieved engraftment had complete hematologic recovery with complete donor chimerism, except for two patients who developed graft failure in 2 months after transplantation. Four cases developed acute grade IIGVHD. The chronic GVHD occurred in 7 of the 16 evaluable cases (6 limited, 1 extensive). 14 patients got disease-free survival with follow-up to January 2012. The disease-free survival rate was 68.9%. It is concluded that the haploidentical or unrelated donor hematopoietic stem cell transplantation may become a viable therapeutic option for severe aplastic anemia patients who lack suitable human leukocyte antigen-matched donors and fail immunosuppressive therapy.

摘要

本研究的目的是评估单倍体相合或非血缘供者造血干细胞移植(HSCT)治疗重型再生障碍性贫血(SAA)患者的疗效和安全性。2005年11月至2011年5月,20例SAA患者接受了来自单倍体相合或非血缘供者的异基因HSCT(14例来自单倍体相合供者,6例来自非血缘供者)。预处理方案包括氟达拉滨(FLU)、环磷酰胺(Cy)和抗胸腺细胞免疫球蛋白(ATG)。患者接受了经粒细胞集落刺激因子(G-CSF)动员的单倍体相合供者骨髓和外周血移植物,或仅接受非血缘供者的外周血移植物。结果显示,中性粒细胞和血小板植入的中位时间分别为14(11 - 20)天和17(13 - 31)天。所有实现植入的患者均获得了完全血液学缓解和完全供者嵌合,除了2例在移植后2个月发生移植物失败的患者。4例发生急性Ⅱ度移植物抗宿主病(GVHD)。16例可评估病例中有7例发生慢性GVHD(6例局限性,1例广泛性)。截至2012年1月,14例患者无病生存。无病生存率为68.9%。结论是,对于缺乏合适的人类白细胞抗原匹配供者且免疫抑制治疗失败的重型再生障碍性贫血患者,单倍体相合或非血缘供者造血干细胞移植可能成为一种可行的治疗选择。

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