Modern management of malignant pleural mesothelioma

IF 5.1 Q1 ONCOLOGY
Shivani Patel, J. Dowell
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引用次数: 32

Abstract

Malignant pleural mesothelioma (MPM) is a deadly disease that produces a significant worldwide health care burden. The majority of cases are associated with prior asbestos exposure, but recent studies have identified a possible genetic predisposition in a minority of patients. Historically, obtaining a pathologic diagnosis of MPM was challenging, but with current pathological techniques, a secure diagnosis is possible in the majority of patients. Curative therapy for MPM remains elusive, and the primary treatment option for fit patients is platinum-based chemotherapy. Encouraging recent reports suggest that there may be a benefit to the addition of bevacizumab to standard chemotherapy as well as with the use of immune checkpoint inhibitors in MPM. Selected patients may be considered for aggressive surgical approaches, but there is considerable controversy regarding the true benefit of surgery and multimodality therapy in this disease.
恶性胸膜间皮瘤的现代治疗
恶性胸膜间皮瘤(MPM)是一种致命的疾病,在世界范围内产生了重大的卫生保健负担。大多数病例与以前接触石棉有关,但最近的研究发现,少数患者可能存在遗传易感性。从历史上看,获得MPM的病理诊断是具有挑战性的,但在目前的病理技术下,大多数患者可以获得可靠的诊断。MPM的治疗方法仍然难以捉摸,适合患者的主要治疗选择是基于铂的化疗。最近令人鼓舞的报道表明,在标准化疗中加入贝伐单抗以及在MPM中使用免疫检查点抑制剂可能有好处。选定的患者可以考虑采用积极的手术方法,但对于这种疾病的手术和多模式治疗的真正益处存在相当大的争议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.10
自引率
0.00%
发文量
10
审稿时长
16 weeks
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