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无关供者脐血移植治疗儿童和青少年非恶性疾病

Unrelated donor cord blood transplantation for non-malignant disorders in children and adolescents.

作者信息

Park Meerim, Lee Young Ho, Kang Hae-Ryong, Lee Ji Won, Kang Hyoung Jin, Park Kyung Duk, Shin Hee Young, Ahn Hyo Seop, Baek Hee Jo, Kook Hoon, Hwang Tai Ju, Lee Jae Wook, Chung Nack-Gyun, Cho Bin, Kim Hack-Ki, Lee Soo Hyun, Yoo Keon Hee, Sung Ki Woong, Koo Hong Hoe, Koh Kyung Nam, Im Ho Joon, Seo Jong Jin, Park Jun Eun, Lim Yeon Jung, Lyu Chuhl Joo, Lee Jae Min, Hah Jeong Ok

机构信息

Department of Pediatrics, Chungbuk National University College of Medicine, Cheongju, South Korea.

出版信息

Pediatr Transplant. 2014 Mar;18(2):221-9. doi: 10.1111/petr.12213. Epub 2013 Dec 30.

Abstract

This study analyzes the data reported to the Korean Cord Blood Registry between 1994 and 2008, involving children and adolescents with non-malignant diseases. Sixty-five patients were evaluated in this study: SAA (n = 24), iBMFS, (n = 16), and primary immune deficiency/inherited metabolic disorder (n = 25). The CI of neutrophil recovery was 73.3% on day 42. By day 100, the CI of acute grade II-IV graft-versus-host disease was 32.3%. At a median follow-up of 71 months, five-yr OS was 50.7%. The survival rate (37.5%) and CI of neutrophil engraftment (37.5%) were lowest in patients with iBMFS. Deaths were mainly due to infection, pulmonary complications, and hemorrhage. In a multivariate analysis, the presence of >3.91 × 10(5) /kg of infused CD34 + cells was the only factor consistently identified as significantly associated with neutrophil engraftment (p = 0.04) and OS (p = 0.03). UCBT using optimal cell doses appears to be a feasible therapy for non-malignant diseases in children and adolescents for whom there is no appropriate HLA-matched related donor. Strategies to reduce transplant-related toxicities would improve the outcomes of UCBT in non-malignant diseases.

摘要

本研究分析了1994年至2008年期间向韩国脐血库报告的数据,这些数据涉及患有非恶性疾病的儿童和青少年。本研究共评估了65例患者:严重再生障碍性贫血(SAA,n = 24)、先天性骨髓衰竭综合征(iBMFS,n = 16)以及原发性免疫缺陷/遗传性代谢紊乱(n = 25)。中性粒细胞恢复的置信区间在第42天为73.3%。到第100天,急性II-IV级移植物抗宿主病的置信区间为32.3%。在中位随访71个月时,5年总生存率为50.7%。iBMFS患者的生存率(37.5%)和中性粒细胞植入的置信区间(37.5%)最低。死亡主要归因于感染、肺部并发症和出血。在多变量分析中,输注的CD34 +细胞>3.91×10(5)/kg是唯一始终被确定与中性粒细胞植入(p = 0.04)和总生存率(p = 0.03)显著相关的因素。对于没有合适的HLA匹配相关供者的儿童和青少年,使用最佳细胞剂量的脐血移植似乎是治疗非恶性疾病的一种可行疗法。降低移植相关毒性的策略将改善脐血移植治疗非恶性疾病的疗效。

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