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A retrospective analysis of haplo-identical HLA-mismatch hematopoietic transplantation without posttransplantation cyclophosphamide for GVHD prophylaxis in patients with adult T-cell leukemia-lymphoma

机译:重新对成虫预防术治疗成人T细胞白血病淋巴瘤患者GVHD预防后环磷酰胺的回顾性分析

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摘要

Currently, allogeneic hematopoietic stem cell transplantation (allo-HCT) is the only available curative modality for patients with adult T-cell leukemia-lymphoma (ATL). When used in conjunction with posttransplantation cyclophosphamide (PTCY) for graft-versus-host disease prophylaxis, allo-HCT from an HLA haplo-identical donor yields promising outcomes for many diseases other than ATL. However, appropriate comparisons with other donor sources, especially cord blood and conventional HLA haplo-identical donors, are needed to validate the safety and efficacy of this modality. In this study, we retrospectively evaluated the outcome of allo-HCT without PTCY in patients with ATL registered in the Japan Society for Hematopoietic Cell Transplantation TRUMP database between 1985 and 2015. During that period, 46 patients received allo-HCT without PTCY and survivors were followed for a median of 2316.5 days (range: 220-3884 days). Although the estimated 1- and 5-year overall survival rates of the entire cohort were 34.5% and 17.7%, respectively, the cumulative 1- and 5-year non-ATL mortality rates of 41.3% and 55.8%, respectively, were high. The results of our study will serve as a platform for discussions of the safety and efficacy of haplo-HCT for future clinical trials in patients with ATL.
机译:目前,同种异体造血干细胞移植(Allo-HCT)是成人T细胞白血病淋巴瘤(ATL)患者的唯一可用的疗效。当与移植物与宿主疾病预防的接枝腔内环磷酰胺(PTCY)结合使用时,来自HLA HLA的相同供体的Allo-HCT产生了许多除ATL以外的许多疾病的有希望的结果。然而,需要适当比较其他供体源,尤其是脐带血和常规HLA HLA相同的供体,以验证这种模态的安全性和功效。在这项研究中,我们回顾性地评估了在1985年至2015年间日本造血细胞移植特朗普数据库的ATL注册的ATL注册患者的血腥-HCT的结果。在此期间,46名患者接受了没有PTCY和幸存者的allo-hct随访中位数为2316.5天(范围:220-388天)。虽然整个队列的估计1和5年整体生存率分别为34.5%和17.7%,累积1 - 和5年的非ATL死亡率分别为41.3%和55.8%,高。我们的研究结果将作为讨论HAPLO-HCT对ATL患者未来临床试验的安全性和疗效的平台。

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