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成人T细胞白血病/淋巴瘤(ATL)

[Adult T cell leukemia/lymphoma (ATL)].

作者信息

Tanosaki Ryuji

机构信息

Division of Laboratory Medicine, National Cancer Center Hospital.

出版信息

Nihon Rinsho. 2003 Sep;61(9):1592-5.

Abstract

Adult T cell leukemia/lymphoma(ATL) is an aggressive, fatal malignancy associated with human T-lymphotropic virus type I(HTLV-I). The median survival time of acute- and lymphoma-type ATL is 6 and 10 months, respectively. According to recent reports, nearly half of the ATL patients who received allogeneic hematopoietic stem cell transplantation could survive without disease for over 3 years. However, the population of patients who are eligible for conventional transplantation is extremely limited. Therefore, a reduced-intensity allogeneic stem cell transplantation(RIST) is applied to ATL patients and a multi-center phase I clinical trial is now underway. In our institute, 5 patients, who received RIST, are all alive, with 1 case relapsed after 6 months. Thus, RIST is considered very promising.

摘要

成人T细胞白血病/淋巴瘤(ATL)是一种侵袭性、致命的恶性肿瘤,与I型人类嗜T淋巴细胞病毒(HTLV-I)相关。急性型和淋巴瘤型ATL的中位生存时间分别为6个月和10个月。根据最近的报告,接受异基因造血干细胞移植的ATL患者中,近一半能够无病存活超过3年。然而,适合传统移植的患者群体极其有限。因此,降低强度的异基因干细胞移植(RIST)被应用于ATL患者,一项多中心I期临床试验正在进行中。在我们研究所,接受RIST的5名患者均存活,其中1例在6个月后复发。因此,RIST被认为非常有前景。

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