首页> 外文期刊>Leukemia and lymphoma >A multi-institutional experience of autologous stem cell transplantation in North American patients with human T-cell lymphotropic virus type-1 adult T-cell leukemia/lymphoma suggests ineffective salvage of relapsed patients.
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A multi-institutional experience of autologous stem cell transplantation in North American patients with human T-cell lymphotropic virus type-1 adult T-cell leukemia/lymphoma suggests ineffective salvage of relapsed patients.

机译:在北美患有1型人类T细胞淋巴病毒的成人T细胞白血病/淋巴瘤患者的自体干细胞移植的多机构经验表明,挽救复发患者无效。

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摘要

Adult T-cell leukemia/lymphoma (ATLL) is a rare T-cell neoplasm caused by the human T-cell lympho-tropic virus type-1 (HTLV-1), a retrovirus endemic in Japan, sub-Saharan Africa and the Caribbean basin. In the U.S., ATLL is primarily seen among immigrants from endemic regions. Patients with the acute and lymphomatous subtypes have the poorest prognosis, with a median survival of only 6-13 months despite aggressive combination chemotherapy [1], Without an established curative regimen, high-dose chemotherapy followed by autologous stem cell transplantation (ASCT) has become a salvage treatment in the relapsed setting [2].
机译:成人T细胞白血病/淋巴瘤(ATLL)是一种罕见的T细胞肿瘤,是由人类T细胞淋巴嗜性病毒1型(HTLV-1)引起的,该病毒是日本,撒哈拉以南非洲和加勒比地区的特有逆转录病毒盆地。在美国,ATLL主要见于来自地方病地区的移民。急性和淋巴瘤亚型患者的预后最差,尽管进行了积极的联合化疗,中位生存期仅为6-13个月[1],如果没有确定的治疗方案,则大剂量化疗后进行自体干细胞移植(ASCT)在复发的情况下成为打捞治疗[2]。

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