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高危急性淋巴细胞白血病患儿脐带血与未处理单倍体造血干细胞移植后结局的比较

Comparison of outcomes after umbilical cord blood and unmanipulated haploidentical hematopoietic stem cell transplantation in children with high-risk acute lymphoblastic leukemia.

作者信息

Mo Xiao-Dong, Tang Bao-Lin, Zhang Xiao-Hui, Zheng Chang-Cheng, Xu Lan-Ping, Zhu Xiao-Yu, Wang Yu, Liu Hui-Lan, Yan Chen-Hua, Chu Xian-Deng, Chen Huan, Geng Liang-Quan, Liu Kai-Yan, Sun Zi-Min, Huang Xiao-Jun

机构信息

Peking University People's Hospital, Peking University Institute of Hematology, Beijing, China.

Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.

出版信息

Int J Cancer. 2016 Nov 1;139(9):2106-15. doi: 10.1002/ijc.30249. Epub 2016 Jul 15.

DOI:10.1002/ijc.30249
PMID:27356906
Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) is an effective therapy for children with high-risk acute lymphoblastic leukemia (ALL). Human leukocyte antigen (HLA)-haploidentical HSCT (haplo-HSCT) or umbilical cord blood transplantation (UCBT) are both important alternative sources of stem cells for those without an HLA-identical sibling donor or unrelated matched donor. We aimed to compare the therapeutic effects of single UCBT and unmanipulated haplo-HSCT in high-risk ALL children (n = 129). Hematopoietic recovery was significantly faster in haplo-HSCT recipients than in UCBT recipients. The 2-year cumulative incidences of relapse in the haplo-HSCT and UCBT groups were 16.1% and 24.1%, respectively (p = 0.169). The 2-year cumulative incidences of non-relapse mortality in the haplo-HSCT and UCBT groups were 12.8% and 18.8%, respectively (p = 0.277). The 2-year probabilities of overall survival in the haplo-HSCT and UCBT groups were 82.0% and 69.6%, respectively (p = 0.071), and the 2-year probability of disease-free survival in the haplo-HSCT group was higher than in the UCBT group (71.0% vs. 57.2%, p = 0.040). However, several variables (such as leukocyte count and cytogenetics at diagnosis) were different between the groups, and a possible center effect should also be considered. In addition, only mild and moderate chronic graft-versus-host disease (GVHD) was associated with significantly improved survival compared to those without chronic GVHD in multivariate analysis. Thus, our results show that both unmanipulated haplo-HSCT and UCBT are valid for high-risk ALL children lacking a HLA matched donor, and both strategies expand the donor pool for children in need.

摘要

异基因造血干细胞移植(HSCT)是治疗高危急性淋巴细胞白血病(ALL)患儿的有效方法。对于没有 HLA 全相合同胞供者或无关匹配供者的患者,人类白细胞抗原(HLA)单倍体相合 HSCT(单倍体 HSCT)或脐带血移植(UCBT)都是重要的干细胞替代来源。我们旨在比较单份 UCBT 和未处理的单倍体 HSCT 对高危 ALL 患儿(n = 129)的治疗效果。单倍体 HSCT 受者的造血恢复明显快于 UCBT 受者。单倍体 HSCT 组和 UCBT 组的 2 年累积复发率分别为 16.1%和 24.1%(p = 0.169)。单倍体 HSCT 组和 UCBT 组的 2 年累积非复发死亡率分别为 12.8%和 18.8%(p = 0.277)。单倍体 HSCT 组和 UCBT 组 的 2 年总生存率分别为 82.0%和 69.6%(p = 0.071),单倍体 HSCT 组的 2 年无病生存率高于 UCBT 组(71.0%对 57.2%,p = 0.040)。然而,两组之间存在几个变量差异(如诊断时的白细胞计数和细胞遗传学),并且还应考虑可能的中心效应。此外,在多变量分析中,与没有慢性移植物抗宿主病(GVHD)的患者相比,只有轻度和中度慢性 GVHD 与生存率显著提高相关。因此,我们的结果表明,未处理的单倍体 HSCT 和 UCBT 对缺乏 HLA 匹配供者的高危 ALL 患儿均有效,这两种策略都扩大了有需要儿童的供者库。

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