Combination of haploidentical haematopoietic stem cell transplantation with an unrelated cord-blood unit in patients with severe aplastic anemia: a report of 146 cases

被引:16
作者
Liu, Limin [1 ]
Zhang, Yanming [2 ,3 ]
Jiao, Wenjing [4 ]
Zhou, Huifen [1 ]
Wang, Qingyuan [1 ]
Qiu, Huiying [1 ]
Tang, Xiaowen [1 ]
Han, Yue [1 ]
Fu, Chengcheng [1 ]
Jin, Zhengming [1 ]
Chen, Suning [1 ]
Sun, Aining [1 ]
Miao, Miao [1 ]
Wu, Depei [1 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Natl Clin Res Ctr Hematol Dis, Jiangsu Inst Hematol, Suzhou, Peoples R China
[2] Xuzhou Med Univ, Affiliated Huaian Hosp, Dept Hematol, 62 Huaihai Rd S, Huaian, Peoples R China
[3] Second Peoples Hosp Huaian, 62 Huaihai Rd S, Huaian, Peoples R China
[4] Xian Yang Cent Hosp, Dept Hematol, Xianyang, Shanxi, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
MARROW-TRANSPLANTATION; ANTITHYMOCYTE GLOBULIN; CONDITIONING REGIMEN; DEPLETION; MULTICENTER; CONSENSUS; CHILDREN; COTRANSPLANTATION; RECONSTITUTION; ADOLESCENTS;
D O I
10.1038/s41409-020-0874-9
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We analyzed the outcomes of 146 severe aplastic anemia (SAA) patients who received a combination of haploidentical haematopoietic stem cell transplantation (haplo-HSCT) and an unrelated cord-blood (UCB) unit between September 2011 and December 2017. One hundred and seventeen patients underwent transplantation as first-line therapy. Seven patients experienced early mortality, and among the evaluable 139 patients, one patient experienced primary graft failure (GF), while the other 138 patients achieved successful haploidentical donor engraftment; additionally, three patients experienced secondary GF. Six patients demonstrated delayed platelet recovery, and three patients demonstrated platelet GF. The median time for myeloid and platelet engraftment was 11 (range: 9-28) days and 15 (range: 9-330) days, respectively. With a median follow-up of 40 (range: 18-93) months, the cumulative incidences were 31.43% and 10.00% for grades II-IV and grades III-IV acute graft-versus-host disease (GVHD), respectively. The cumulative incidences of chronic GVHD (cGVHD) and moderate-severe cGVHD were 36.23% and 11.71%, respectively. There was no patient relapse. The probabilities of 4-year overall survival and GVHD-free, failure-free survival were 81.4 +/- 3.3% and 69.2 +/- 3.9%, respectively. These encouraging preliminary results indicated that haplo-HSCT combined with the infusion of UCB is a feasible choice for SAA patients without matched donors.
引用
收藏
页码:2017 / 2025
页数:9
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