恶性胸膜间皮瘤的免疫治疗:一个漫长的故事以成功告终

IF 1.4 Q4 ONCOLOGY
Alberto Bongiovanni, A. Frassoldati, L. Calabrò
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引用次数: 1

摘要

恶性胸膜间皮瘤(MPM)是一种罕见的侵袭性疾病,主要由石棉暴露引起,其特点是预后差。近二十年来,铂类化疗一直是唯一被批准的一线MPM治疗方案,总生存期为12个月。在过去的几年中,由于免疫检查点抑制,包括MPM在内的不同类型肿瘤的治疗方案发生了巨大的变化。这种方法的有希望的结果促进了临床研究的新努力,许多研究新的治疗组合的试验目前正在进行中。本综述的目的是提供目前正在研究的晚期MPM最有前途的基于免疫治疗的策略的全面概述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunotherapy in malignant pleural mesothelioma: a long story ended in success
Malignant pleural mesothelioma (MPM) is an aggressive and rare disease, mainly due to asbestos exposure, characterized by a poor prognosis. For almost two decades, platinum-based chemotherapy has been the only approved therapeutic regimen for first-line MPM, with an overall survival of 12 months. In the last years, the therapeutic scenario of different tumor types, including MPM, has dramatically changed due to immune checkpoint inhibition. The promising results of this approach have promoted new efforts into clinical research, and many trials investigating novel therapeutic combinations are currently ongoing. The aim of the present review is to provide a comprehensive overview of the most promising immunotherapeutic-based strategies currently under investigation for advanced MPM.
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CiteScore
3.20
自引率
5.30%
发文量
460
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