Department of Oncology, University of Turin, San Luigi Gonzaga Hospital, Orbassano, 10124 Turin, Italy.
Department of Medical Oncology, Cardinal Massaia Hospital, 14100 Asti, Italy.
Cells. 2022 Feb 25;11(5):803. doi: 10.3390/cells11050803.
Significant progress has been achieved over the last decades in understanding the biology and mechanisms of tumor progression in urothelial carcinoma (UC). Although the therapeutic landscape has dramatically changed in recent years with the introduction of immune checkpoint inhibitors, advanced UC is still associated with rapidly progressing disease and poor survival. The increasing knowledge of the pathogenesis and molecular pathways underlying cancer development and progression is leading the introduction of target therapies, such as the recently approved FGFR inhibitor Erdafitinib, or the anti-nectin 4 antibody drug-conjugate Enfortumab vedotin. Antibody drug conjugates represent an innovative therapeutic approach that allows the combination of a tar get-specific monoclonal antibody covalently conjugated via a linker to a cytotoxic agent (payload). UC is a perfect candidate for this therapeutic approach since it is particularly enriched in antigen expression on its surface and each specific antigen can represent a potential therapeutic target. In this review we summarize the mechanism of action of ADCs, their applications in localized and metastatic UC, the main mechanisms of resistance, and future perspectives for their use in clinical practice.
在过去几十年中,人们在理解尿路上皮癌(UC)的生物学和机制方面取得了重大进展。尽管近年来随着免疫检查点抑制剂的引入,治疗领域发生了巨大变化,但晚期 UC 仍然与疾病迅速进展和生存不良有关。对癌症发生和发展的发病机制和分子途径的深入了解正在推动靶向治疗的引入,例如最近批准的 FGFR 抑制剂 Erdafitinib,或抗 nectin 4 抗体药物偶联物 Enfortumab vedotin。抗体药物偶联物代表了一种创新的治疗方法,它允许通过连接子将靶向特异性单克隆抗体与细胞毒性药物(有效载荷)共价连接。UC 是这种治疗方法的理想候选者,因为它在其表面特别富含抗原表达,并且每个特定抗原都可以代表一个潜在的治疗靶点。在这篇综述中,我们总结了 ADC 的作用机制、它们在局限性和转移性 UC 中的应用、主要的耐药机制以及它们在临床实践中的未来应用前景。