Bertoli Elisa, De Carlo Elisa, Bortolot Martina, Stanzione Brigida, Del Conte Alessandro, Spina Michele, Bearz Alessandra
Department of Medical Oncology, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, 33081 Aviano, Italy.
Department of Medicine, University of Udine, 33100 Udine, Italy.
Cancers (Basel). 2024 May 22;16(11):1971. doi: 10.3390/cancers16111971.
Mesothelioma (MM) is an aggressive and lethal disease with few therapeutic opportunities. Platinum-pemetrexed chemotherapy is the backbone of first-line treatment for MM. The introduction of immunotherapy (IO) has been the only novelty of the last decades, allowing an increase in survival compared to standard chemotherapy (CT). However, IO is not approved for epithelioid histology in many countries. Therefore, therapy for relapsed MM remains an unmet clinical need, and the prognosis of MM remains poor, with an average survival of only 18 months. Increasing evidence reveals MM complexity and heterogeneity, of which histological classification fails to explain. Thus, scientific focus on possibly new molecular markers or cellular targets is increasing, together with the search for target therapies directed towards them. The molecular landscape of MM is characterized by inactivating tumor suppressor alterations, the most common of which is found in CDKN2A, BAP1, MTAP, and NF2. In addition, cellular targets such as mesothelin or metabolic enzymes such as ASS1 could be potentially amenable to specific therapies. This review examines the major targets and relative attempts of therapeutic approaches to provide an overview of the potential prospects for treating this rare neoplasm.
间皮瘤(MM)是一种侵袭性致死性疾病,治疗机会有限。铂类培美曲塞化疗是MM一线治疗的基础。免疫疗法(IO)的引入是过去几十年中唯一的新进展,与标准化疗(CT)相比,可提高生存率。然而,在许多国家,IO尚未被批准用于上皮样组织学类型。因此,复发MM的治疗仍然是未满足的临床需求,MM的预后仍然很差,平均生存期仅为18个月。越来越多的证据揭示了MM的复杂性和异质性,而组织学分类无法解释这些。因此,对可能的新分子标志物或细胞靶点的科学关注日益增加,同时也在寻找针对它们的靶向治疗方法。MM的分子图谱特征是肿瘤抑制因子失活改变,其中最常见的发生在CDKN2A、BAP1、MTAP和NF2中。此外,间皮素等细胞靶点或ASS1等代谢酶可能适合特定治疗。本综述探讨了主要靶点及治疗方法的相关尝试,以概述治疗这种罕见肿瘤的潜在前景。