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Improved outcome of refractory Langerhans cell histiocytosis in children with hematopoietic stem cell transplantation in Japan.

机译:日本造血干细胞移植患儿难治性朗格汉斯细胞组织细胞增生的改善结果。

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摘要

Langerhans cell histiocytosis (LCH) that is refractory to conventional chemotherapy has a poor outcome. Hematopoietic stem cell transplantation (SCT) is a promising approach for refractory LCH because of its immunomodulatory effect. In this study, the outcomes of children with refractory LCH undergoing SCT in Japan were analyzed. Between November 1995 and March 2007, 15 children younger than 15 years (9 males, 6 females) with refractory LCH underwent SCT. The patients' median age at diagnosis was 8 months (range, 28 days to 28 months), and all had failed conventional chemotherapy. The median age at SCT was 23 months (range, 13-178 months). Nine had risk organ involvement at diagnosis, including liver (n=6), spleen (n=5), lung (n=5), and/or hematopoietic system (n=4). For SCT, a myeloablative regimen was used for 10 patients, and a reduced-intensity conditioning regimen (RIC) was used for five. The donor source varied among the patients, but allogeneic cord blood was primarily used (n=10). Subsequently, 11 of 15 patients have survived with no evidence of disease, with a 10-year overall survival (OS) rate (median+/-standard error) of 73.3+/-11.4%. The 10-year OS rate of nine patients with risk organ involvement at diagnosis was 55.6+/-16.6%, whereas six without risk organ involvement have all survived with no evidence of disease (P=0.07). These results indicate that SCT is promising as a salvage approach for children with refractory LCH.
机译:传统化学疗法难治的朗格汉斯细胞组织细胞增生症(LCH)的预后不良。造血干细胞移植(SCT)由于其免疫调节作用,是治疗难治性LCH的有前途的方法。在这项研究中,分析了在日本进行SCT的难治性LCH儿童的结局。在1995年11月至2007年3月之间,对15例15岁以下的难治性LCH儿童(男9例,女6例)进行了SCT。患者的诊断中位年龄为8个月(范围28天至28个月),所有患者均未接受常规化疗。 SCT的中位年龄为23个月(范围13-178个月)。有9个在诊断时有风险器官受累,包括肝脏(n = 6),脾脏(n = 5),肺(n = 5)和/或造血系统(n = 4)。对于SCT,10例患者使用了清髓治疗方案,而5例使用了低强度条件治疗方案(RIC)。不同患者的供体来源不同,但主要使用异体脐带血(n = 10)。随后,在15名患者中有11名幸存下来,没有任何疾病的证据,其10年总生存率(中位数标准误)为73.3 +/- 11.4%。 9名诊断为有风险器官受累的患者的10年OS率为55.6 +/- 16.6%,而6例无风险器官受累的患者全部存活,没有疾病的证据(P = 0.07)。这些结果表明,SCT有望作为顽固性LCH患儿的救治方法。

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