Department of Oncology and Hematology, Azienda Ospedaliero-Universitaria di Modena, 41124 Modena, Italy.
Department of Medical and Surgical Sciences, University of Modena and Reggio Emilia, 41124 Modena, Italy.
Genes (Basel). 2023 Mar 9;14(3):684. doi: 10.3390/genes14030684.
Hereditary cancer syndromes are inherited disorders caused by germline pathogenic variants (PVs) that lead to an increased risk of developing certain types of cancer, frequently at an earlier age than in the rest of the population. The germline PVs promote cancer development, growth and survival, and may represent an ideal target for the personalized treatment of hereditary tumors. PARP inhibitors for the treatment of BRCA and PALB2-associated tumors, immune checkpoint inhibitors for tumors associated with the Lynch Syndrome, HIF-2α inhibitor in the VHL-related cancers and, finally, selective RET inhibitors for the treatment of MEN2-associated medullary thyroid cancer are the most successful examples of how a germline PVs can be exploited to develop effective personalized therapies and improve the outcome of these patients. The present review aims to describe and discuss the personalized systemic therapies for inherited cancer syndromes that have been developed and investigated in clinical trials in recent decades.
遗传性癌症综合征是由种系致病性变异(PVs)引起的遗传疾病,导致某些类型的癌症风险增加,通常比普通人群更早发病。种系 PVs 促进癌症的发展、生长和存活,可能是遗传性肿瘤个体化治疗的理想靶点。PARP 抑制剂治疗 BRCA 和 PALB2 相关肿瘤、免疫检查点抑制剂治疗 Lynch 综合征相关肿瘤、VHL 相关癌症的 HIF-2α 抑制剂,以及最后用于治疗 MEN2 相关甲状腺髓样癌的选择性 RET 抑制剂,这些都是如何利用种系 PVs 开发有效个体化治疗方法并改善这些患者预后的最成功例子。本综述旨在描述和讨论近几十年来在临床试验中开发和研究的遗传性癌症综合征的个体化系统治疗方法。