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成人 T 细胞白血病:当前和有前途的治疗方法的全面概述。

Adult T-Cell Leukemia: a Comprehensive Overview on Current and Promising Treatment Modalities.

机构信息

Department of Internal Medicine, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.

Department of Anatomy, Cell Biology and Physiological Sciences, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.

出版信息

Curr Oncol Rep. 2021 Nov 4;23(12):141. doi: 10.1007/s11912-021-01138-3.

Abstract

PURPOSE OF THE REVIEW

Adult T-cell leukemia (ATL) is an aggressive chemo-resistant malignancy secondary to HTLV-1 retrovirus. Prognosis of ATL remains dismal. Herein, we emphasized on the current ATL treatment modalities and their drawbacks, and opened up on promising targeted therapies with special focus on the HTLV-1 regulatory proteins Tax and HBZ.

RECENT FINDINGS

Indolent ATL and a fraction of acute ATL exhibit long-term survival following antiviral treatment with zidovudine and interferon-alpha. Monoclonal antibodies such as mogamulizumab improved response rates, but with little effect on survival. Allogeneic hematopoietic cell transplantation results in long-term survival in one third of transplanted patients, alas only few patients are transplanted. Salvage therapy with lenalidomide in relapsed/refractory patients leads to prolonged survival in some of them. ATL remains an unmet medical need. Targeted therapies focusing on the HTLV-1 viral replication and/or viral regulatory proteins, as well as on the host antiviral immunity, represent a promising approach for the treatment of ATL.

摘要

目的综述

成人 T 细胞白血病(ATL)是一种由 HTLV-1 逆转录病毒引起的侵袭性、耐药性恶性肿瘤。ATL 的预后仍然很差。在此,我们强调了目前 ATL 的治疗方法及其缺点,并探讨了有前途的靶向治疗方法,特别关注 HTLV-1 调节蛋白 Tax 和 HBZ。

最新发现

接受齐多夫定和干扰素-α抗病毒治疗后,惰性 ATL 和一部分急性 ATL 可长期生存。单克隆抗体如 mogamulizumab 可提高缓解率,但对生存影响不大。异基因造血细胞移植可使三分之一的移植患者长期生存,但只有少数患者接受移植。对于复发/难治性患者,用来那度胺进行挽救治疗可使其中一些患者的生存期延长。ATL 仍然是一个未满足的医疗需求。针对 HTLV-1 病毒复制和/或病毒调节蛋白以及宿主抗病毒免疫的靶向治疗方法,代表了治疗 ATL 的一种很有前途的方法。

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