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采用 CliniMACs 分选的超大剂量 CD34+细胞和固定 CD3+剂量的单倍体相关供者造血细胞移植治疗儿童

Haploidentical related-donor hematopoietic cell transplantation in children using megadoses of CliniMACs-selected CD34(+) cells and a fixed CD3(+) dose.

机构信息

Department of Pediatrics, Division of Allergy, Immunology, and Blood and Marrow Transplant, UCSF Benioff Children's Hospital, University of California San Francisco, San Francisco, CA 94143-1278, USA.

出版信息

Bone Marrow Transplant. 2013 Apr;48(4):508-13. doi: 10.1038/bmt.2012.186. Epub 2012 Nov 26.

Abstract

We conducted a prospective phase II trial utilizing the CliniMACs system to perform CD34(+)-cell selection of PBSCs from haploidentical donors to evaluate engraftment and hematoimmunological reconstitution. In total, 21 children with hematological malignancies or nonmalignant conditions underwent conditioning with 1200 cGy TBI, thiotepa, fludarabine and Thymoglobulin. Patients received megadoses of CD34(+) cells (median: 22 × 10(6)/kg) with a fixed dose of 3 × 10(4)/kg CD3(+) cells/kg, and engraftment occurred in 90% with prompt recovery of neutrophils and platelets. Grade II acute GVHD (aGVHD) was seen in 32% (95% confidence interval (CI), 15-54%) of evaluable patients, there was no grade III-IV aGVHD, and chronic extensive GVHD was seen in 35% (95% CI, 17-59%) of patients. The estimated 2-year EFS was 62% (95% CI, 48-83%) with a median survivor follow-up of 49 months (range: 18-119 months). Patients with nonmalignant diseases had an estimated 2-year EFS of 100% (95% CI, 56-100%) and patients with malignancies in remission had an estimated 2-year EFS of 56% (95% CI, 22-89%). Megadose CD34(+) cells with a fixed CD3(+) cell dose from haploidentical related donors resulted in good outcomes for pediatric patients with nonmalignant diseases and those with malignant diseases transplanted in remission.

摘要

我们进行了一项前瞻性 II 期试验,使用 CliniMACs 系统从半相合供者的 PBSC 中进行 CD34(+)细胞选择,以评估植入和血液免疫重建。共有 21 名患有血液系统恶性肿瘤或非恶性疾病的儿童接受了 1200cGyTBI、噻替哌、氟达拉滨和 Thymoglobulin 的预处理。患者接受了大量 CD34(+)细胞(中位数:22×10(6)/kg)和固定剂量的 3×10(4)/kg CD3(+)细胞/kg,90%的患者发生了植入,中性粒细胞和血小板迅速恢复。32%(95%可信区间(CI),15-54%)可评估患者出现 II 级急性移植物抗宿主病(aGVHD),无 III-IV 级 aGVHD,35%(95%CI,17-59%)的患者出现慢性广泛型 GVHD。估计 2 年无事件生存率(EFS)为 62%(95%CI,48-83%),中位随访时间为 49 个月(范围:18-119 个月)。非恶性疾病患者的估计 2 年 EFS 为 100%(95%CI,56-100%),缓解期恶性疾病患者的估计 2 年 EFS 为 56%(95%CI,22-89%)。来自半相合相关供者的大量 CD34(+)细胞与固定的 CD3(+)细胞剂量相结合,为非恶性疾病和缓解期恶性疾病的儿科患者带来了良好的结果。

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