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儿科相关和不相关的脐带血移植治疗恶性疾病。

Pediatric related and unrelated cord blood transplantation for malignant diseases.

机构信息

Hôpital Saint Louis, Paris, France.

出版信息

Bone Marrow Transplant. 2009 Nov;44(10):653-9. doi: 10.1038/bmt.2009.291. Epub 2009 Oct 5.

Abstract

The use of umbilical or placental donor cord blood transplantation (CBT) in children with malignant and non-malignant diseases has witnessed important progress, mainly because of better cord blood donor choice and patient selection translating into better patient outcome. Approximately 2000 children with malignant diseases (about 75 % with acute leukemias) have been transplanted with a related (n=199) or unrelated CBT (UCBT, n=1663) and reported to Eurocord registry from 1990-2008. Disease-specific studies have been carried out after UCBT for acute lymphoblastic and myeloid leukemia and myelodysplastic syndromes in others to identify the risk factors that may improve outcomes. Outcomes after CBT have been compared with other alternative allogeneic hematopoietic SCT (HSCT) donors. Briefly, after CBT, myeloid engraftment is delayed, acute and chronic GVHD decreased and disease-free survival was not statistically different when compared with HLA identical and other alternative HSCT donor. Therefore, any physician has to carefully evaluate, for each single pediatric patient in need of an allograft, all the possible alternatives in order to choose the best hematopoietic stem cell donor, taking into account type of disease, urgency of transplantation, donor characteristics and center experience. This review will analyze the current results of CBT for pediatric patients with malignant diseases and the advantages and limitations of using this stem cell source.

摘要

脐带或胎盘供者脐血移植(CBT)在儿童恶性和非恶性疾病中的应用取得了重要进展,主要是因为更好的脐带血供者选择和患者选择转化为更好的患者结果。大约 2000 名患有恶性疾病(约 75%为急性白血病)的儿童已接受相关(n=199)或无关 CBT(UCBT,n=1663)移植,并于 1990 年至 2008 年向 Eurocord 登记处报告。在 UCBT 后进行了急性淋巴细胞白血病和髓性白血病以及其他骨髓增生异常综合征的疾病特异性研究,以确定可能改善结果的危险因素。CBT 后的结果与其他替代同种异体造血干细胞移植(HSCT)供体进行了比较。简而言之,与 HLA 相同和其他替代 HSCT 供体相比,CBT 后骨髓植入延迟,急性和慢性移植物抗宿主病减少,无病生存率无统计学差异。因此,任何医生都必须仔细评估每个需要同种异体移植的儿科患者的所有可能替代方案,以选择最佳的造血干细胞供者,同时考虑疾病类型、移植紧迫性、供者特征和中心经验。这篇综述将分析 CBT 在儿科恶性疾病患者中的当前结果,以及使用这种干细胞来源的优势和局限性。

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