Yun Karen M, Bazhenova Lyudmila
Division of Hematology-Oncology, Moores Cancer Center at UC San Diego Health, La Jolla, CA 92093, USA.
Cancers (Basel). 2024 Mar 22;16(7):1252. doi: 10.3390/cancers16071252.
Malignant pleural mesothelioma (MPM) is a heterogeneous cancer composed of distinct molecular and pathologic subtypes. Unfortunately, MPM is aggressive, and current therapies for advanced, unresectable disease remain limited to cytotoxic chemotherapy and immunotherapy. Our understanding of the genomic landscape of MPM is steadily growing, while the discovery of effective targeted therapies in MPM has advanced more slowly than in other solid tumors. Given the prevalence of alterations in tumor suppressor genes in MPM, it has been challenging to identify actionable targets. However, efforts to characterize the genetic signatures in MPM over the last decade have led to a range of novel targeted therapeutics entering early-phase clinical trials. In this review, we discuss the advancements made thus far in targeted systemic therapies in MPM and the future direction of targeted strategies in patients with advanced MPM.
恶性胸膜间皮瘤(MPM)是一种由不同分子和病理亚型组成的异质性癌症。不幸的是,MPM具有侵袭性,目前针对晚期、不可切除疾病的治疗仍局限于细胞毒性化疗和免疫疗法。我们对MPM基因组格局的了解在不断增加,而MPM中有效靶向治疗的发现比其他实体瘤进展得更缓慢。鉴于MPM中肿瘤抑制基因改变的普遍性,确定可操作的靶点一直具有挑战性。然而,在过去十年中对MPM基因特征进行表征的努力已促使一系列新型靶向疗法进入早期临床试验。在这篇综述中,我们讨论了MPM靶向全身治疗迄今取得的进展以及晚期MPM患者靶向治疗策略的未来方向。