恶性胸膜间皮瘤全身治疗的最新进展:集中于抗血管生成抑制剂和免疫检查点抑制剂

Fumie Onishi, N. Fujimoto
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引用次数: 0

摘要

恶性胸膜间皮瘤(MPM)是一种与过去接触石棉密切相关的肿瘤。一般情况下,MPM患者预后较差;然而,近年来,已经报道了一些令人鼓舞的全身治疗MPM的结果。在一项随机III期研究中,与标准的铂基化疗相比,nivolumab和ipilimumab联合治疗提高了总生存率。一个重要的临床问题是免疫疗法联合细胞毒性化疗和/或血管生成抑制剂是否可以进一步改善MPM患者的预后。本章涵盖了系统治疗的最新发现,包括细胞毒性化疗、抗血管生成抑制剂和/或免疫检查点抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent Advances in Systemic Therapy for Malignant Pleural Mesothelioma: Focus on Anti-Angiogenic Inhibitors and Immune Checkpoint Inhibitors
Malignant pleural mesothelioma (MPM) is a neoplasm strongly associated with past exposure to asbestos. In general, the prognosis of patients with MPM is poor; however, in recent years, some encouraging results have been reported for systemic therapies for MPM. In a randomized phase III study, the combination of nivolumab and ipilimumab improved overall survival, compared to the standard platinum-based chemotherapy. An important clinical issue is whether the outcome of patients with MPM might be further improved by combining immunotherapies with cytotoxic chemotherapy and/or angiogenesis inhibitors. This chapter covers recent findings on systemic therapies, including cytotoxic chemotherapy, anti-angiogenic inhibitors, and/or immune checkpoint inhibitors.
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