Fanale Daniele, Corsini Lidia Rita, Piraino Paola, Pedone Erika, Brando Chiara, Bazan Russo Tancredi Didier, Ferraro Pietro, Simone Alisia, Contino Silvia, Prestifilippo Ornella, Randazzo Ugo, Giurintano Ambra, Ferrante Bannera Carla, Galvano Antonio, Incorvaia Lorena, Pernice Gianfranco, Vieni Salvatore, Pantuso Gianni, Cipolla Calogero, Giannone Antonino Giulio, Badalamenti Giuseppe, Russo Antonio, Bazan Viviana
Section of Medical Oncology, Department of Precision Medicine in Medical, Surgical and Critical Care (Me.Pre.C.C.), University of Palermo, Palermo, Italy.
U.O. Oncologia, Fondazione Istituto G. Giglio, Palermo, Italy.
Front Oncol. 2025 Aug 27;15:1633260. doi: 10.3389/fonc.2025.1633260. eCollection 2025.
Endometrial carcinoma (EC) is one of the most common gynecological cancers showing a survival rate of 15-17% in the case of advanced disease. Based on the mutational burden and copy number alteration, EC is classified into four different molecular subgroups: -mutated (ultramutated), microsatellite unstable (hypermutated), low copy number (endometrioid), and high copy number (serous-like). Despite the high tumor grading, the ultramutated subtype, accounting for about 8-10% of all ECs, showed favorable prognostic potential, enhanced immune response, and excellent clinical outcomes. Somatic POLE alterations have been found in 6-10% of ECs, whereas germline pathogenic variants have been reported only in 0.25-4% of cases. Germline alterations are linked to genome instability and are associated with onset of hereditary tumors, including colorectal cancer and EC. Emerging data suggests that knowledge of mutational status could be clinically important, as ultramutated ECs may be more likely to respond to immunotherapy. In this Review, we will investigate the role of germline/somatic genetic alterations in EC, discussing the potential future theranostic applications and evaluating the benefit of performing a routine genetic testing, in order to adopt prevention and surveillance strategies in germline mutation carriers.
子宫内膜癌(EC)是最常见的妇科癌症之一,晚期疾病的生存率为15%-17%。根据突变负担和拷贝数改变,EC被分为四个不同的分子亚组:POLE突变型(超突变型)、微卫星不稳定型(高突变型)、低拷贝数型(子宫内膜样)和高拷贝数型(浆液性样)。尽管肿瘤分级高,但超突变亚型约占所有EC的8%-10%,显示出良好的预后潜力、增强的免疫反应和出色的临床结果。在6%-10%的EC中发现了体细胞POLE改变,而种系致病性变异仅在0.25%-4%的病例中报道。种系改变与基因组不稳定有关,并与遗传性肿瘤的发生有关,包括结直肠癌和EC。新出现的数据表明,了解突变状态可能具有临床重要性,因为超突变EC可能更有可能对免疫疗法产生反应。在本综述中,我们将研究种系/体细胞基因改变在EC中的作用,讨论潜在的未来治疗诊断应用,并评估进行常规基因检测的益处,以便在种系突变携带者中采取预防和监测策略。