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首页> 外文期刊>International Journal of Hematology >Allogeneic hematopoietic stem cell transplantation for ATL with central nervous system involvement: The Nagasaki Transplant Group experience
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Allogeneic hematopoietic stem cell transplantation for ATL with central nervous system involvement: The Nagasaki Transplant Group experience

机译:涉及中枢神经系统的ATL同种异体造血干细胞移植:长崎移植小组的经验

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Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is regarded as a curative option for aggressive adult T cell leukemia-lymphoma (ATL). However, the efficacy and safety of allo-HSCT for ATL with central nervous system (CNS) involvement, which is highly resistant to chemotherapy, remain controversial. We analyzed 10 ATL patients with CNS involvement who received allo-HSCT at three institutions in Nagasaki prefecture between 2000 and 2007. The 3-year overall survival rate was 40%, and the median observation time of the four surviving patients was 1532 days (range 945–2212 days). Two of four surviving patients received highly intensive local treatment for the CNS; one with 26 intrathecal injections of antineoplastic agents, and the other with whole cerebrospinal irradiation before transplantation. However, the other two patients received conventional or reduced-intensity conditioning with standard intrathecal chemotherapy. Three of the four surviving patients experienced chronic GVHD, and two of three patients with grade 3 or 4 acute GVHD were free from CNS relapse. From these data, it seems that both intensive local treatment for CNS disease and systemic GVHD contributed to the long-term control of CNS involvement. Although our data suggest that allo-HSCT is a therapeutic option for ATL with CNS disease, high transplant-related mortality (six cases) indicates the need for further studies to develop more effective procedures for CNS disease, and to reduce transplant-related morbidity.
机译:异基因造血干细胞移植(allo-HSCT)被认为是侵袭性成人T细胞白血病-淋巴瘤(ATL)的治疗选择。然而,对于对化疗高度耐药的中枢神经系统(CNS)的ATL,异源HSCT的疗效和安全性仍存在争议。我们分析了2000年至2007年之间在长崎县的3个机构中接受allo-HSCT的10名CNS参与的ATL患者。3年总生存率为40%,四名幸存患者的中位观察时间为1532天(范围945-2212天)。四名幸存的患者中有两人接受了高度强化的中枢神经系统局部治疗。一种在鞘内注射抗肿瘤药26次,另一种在移植前进行全脑脊髓照射。但是,其他两名患者接受了常规鞘内化疗或强度降低的标准鞘内化疗。幸存的四名患者中有三名患有慢性GVHD,三名具有3或4级急性GVHD的患者中有2名没有CNS复发。从这些数据来看,似乎中枢神经系统疾病的局部强化治疗和全身性GVHD都有助于中枢神经系统受累的长期控制。尽管我们的数据表明同种异体造血干细胞移植是具有中枢神经系统疾病的ATL的治疗选择,但是高的移植相关死亡率(6例)表明需要进一步研究以开发出更有效的中枢神经系统疾病程序,并减少与移植相关的发病率。

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