Mielgo-Rubio Xabier, Cardeña Gutiérrez Ana, Sotelo Peña Verónica, Sánchez Becerra Maria Virginia, González López Andrea María, Rosero Adriana, Trujillo-Reyes Juan Carlos, Couñago Felipe
Department of Medical Oncology, Hospital Universitario Fundación Alcorcón, Alcorcón 28922, Madrid, Spain.
Department of Medical Oncology, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Canarias 38010, Spain.
World J Clin Oncol. 2022 Apr 24;13(4):267-275. doi: 10.5306/wjco.v13.i4.267.
Malignant pleural mesothelioma (MPM) is the most common type of malignant mesothelioma. It is a rare tumor linked to asbestos exposure and is associated with a poor prognosis. Until very recently, patients with advanced or unresectable disease had limited treatment options, primarily based on doublet chemotherapy with cisplatin and pemetrexed. In 2020 and 2021, after more than a decade with no major advances or new drugs, two phase III clinical trials published results positioning immunotherapy as a promising option for the first- and second-line treatment of MPM. Immunotherapy has revolutionized the treatment of many cancers and is also showing encouraging results in malignant mesothelioma. Both immune checkpoint inhibition and dual cytotoxic T-lymphocyte-associated antigen 4 and programmed death-ligand 1 pathway blockade resulted in significantly improved overall survival in randomized phase III trials. In the CheckMate 743 trial, first-line therapy with nivolumab plus ipilimumab outperformed standard chemotherapy, while in the CONFIRM trial, nivolumab outperformed placebo in patients previously treated with chemotherapy. These two trials represent a major milestone in the treatment of MPM and are set to position immunotherapy as a viable alternative for treatment-naïve patients and patients with progressive disease after chemotherapy.
恶性胸膜间皮瘤(MPM)是最常见的恶性间皮瘤类型。它是一种与石棉暴露相关的罕见肿瘤,预后较差。直到最近,晚期或不可切除疾病的患者治疗选择有限,主要基于顺铂和培美曲塞的双联化疗。在经历了十多年没有重大进展或新药的情况后,2020年和2021年,两项III期临床试验公布了结果,将免疫疗法定位为MPM一线和二线治疗的有前景选择。免疫疗法彻底改变了许多癌症的治疗方式,在恶性间皮瘤中也显示出令人鼓舞的结果。在随机III期试验中,免疫检查点抑制以及双重细胞毒性T淋巴细胞相关抗原4和程序性死亡配体1通路阻断均导致总生存期显著改善。在CheckMate 743试验中,纳武利尤单抗加伊匹木单抗的一线治疗优于标准化疗,而在CONFIRM试验中,纳武利尤单抗在先前接受化疗的患者中优于安慰剂。这两项试验代表了MPM治疗的一个重要里程碑,并将使免疫疗法成为初治患者和化疗后疾病进展患者的可行替代治疗方法。