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胸膜间皮瘤:发病机制、诊断、治疗、预后及生存情况

Pleural Mesothelioma: Pathogenesis, Diagnosis, Treatment, Prognosis, and Survival.

作者信息

Zhang Libo, Huang Meijuan

机构信息

Division of Thoracic Tumor Multimodality Treatment and Department of Medical Oncology Cancer Center West China Hospital Sichuan University Chengdu Sichuan Province China.

出版信息

MedComm (2020). 2025 Sep 1;6(9):e70327. doi: 10.1002/mco2.70327. eCollection 2025 Sep.

Abstract

Pleural mesothelioma (PM) presents significant challenges in clinical management, with current treatment options such as chemotherapy, anti-angiogenic therapies, and immunotherapies only modestly extending progression-free survival (PFS) and overall survival (OS). Another relevant reason is the absence of subsequent-line therapy strategies following progression of PM after approved therapy. Despite extensive research efforts, the development of effective targeted therapies has proven difficult, as most identified mutations in PM tend to be tumor suppressors rather than the driving mutations seen in other cancers. This review aims to provide an in-depth analysis of the biological mechanisms of PM, focusing on genetic alterations, the tumor's immune microenvironment, and dysregulated signaling pathways that contribute to tumorigenesis and resistance to treatment. Additionally, we discuss the growing importance of biomarkers for patient stratification and the development of personalized therapeutic approaches tailored to individual molecular profiles. We also explore promising avenues for novel therapeutic strategies, such as combination therapies and immunotherapeutic interventions. By integrating insights from both basic and clinical research, this review seeks to present a comprehensive framework for understanding PM and advancing its therapeutic management, ultimately aiming to improve patient outcomes through more effective and targeted treatment approaches.

摘要

胸膜间皮瘤(PM)在临床管理上面临重大挑战,目前的治疗选择如化疗、抗血管生成疗法和免疫疗法仅适度延长了无进展生存期(PFS)和总生存期(OS)。另一个相关原因是在批准的治疗后PM进展后缺乏后续治疗策略。尽管进行了广泛的研究,但事实证明开发有效的靶向疗法很困难,因为在PM中鉴定出的大多数突变往往是肿瘤抑制基因,而不是其他癌症中所见的驱动突变。本综述旨在深入分析PM的生物学机制,重点关注基因改变、肿瘤免疫微环境以及导致肿瘤发生和治疗耐药的失调信号通路。此外,我们讨论了生物标志物在患者分层中的重要性日益增加以及针对个体分子特征开发个性化治疗方法。我们还探索了新型治疗策略的有前景途径,如联合疗法和免疫治疗干预。通过整合基础研究和临床研究的见解,本综述旨在提出一个全面的框架来理解PM并推进其治疗管理,最终目标是通过更有效和有针对性的治疗方法改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5427/12402622/2f4bb729b36a/MCO2-6-e70327-g004.jpg

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