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

被引:49
|
作者
Mo, Xiao-Dong [1 ,2 ]
Tang, Bao-Lin [3 ]
Zhang, Xiao-Hui [1 ,2 ]
Zheng, Chang-Cheng [3 ]
Xu, Lan-Ping [1 ,2 ]
Zhu, Xiao-Yu [3 ]
Wang, Yu [1 ,2 ]
Liu, Hui-Lan [3 ]
Yan, Chen-Hua [1 ,2 ]
Chu, Xian-Deng [3 ]
Chen, Huan [1 ,2 ]
Geng, Liang-Quan [3 ]
Liu, Kai-Yan [1 ,2 ]
Sun, Zi-Min [3 ]
Huang, Xiao-Jun [1 ,2 ,4 ]
机构
[1] Peking Univ, Peoples Hosp, Inst Hematol, 11 Xizhimen South St, Beijing 100044, Peoples R China
[2] Beijing Key Lab Hematopoiet Stem Cell Transplanta, Beijing, Peoples R China
[3] Anhui Med Univ, Anhui Prov Hosp, Dept Hematol, Lujiang Rd 19, Hefei 230001, Peoples R China
[4] Peking Tsinghua Ctr Life Sci, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
umbilical cord blood transplantation; stem cell transplantation; haploidentical; children; acute lymphoblastic leukemia; VERSUS-HOST-DISEASE; DONOR LYMPHOCYTE INFUSION; BONE-MARROW; MYELOID-LEUKEMIA; NERVOUS-SYSTEM; FREE SURVIVAL; CHRONIC GVHD; DEPLETION; RELAPSE; REMISSION;
D O I
10.1002/ijc.30249
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:2106 / 2115
页数:10
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