Department of Biology and Biochemistry, University of Bath, Bath, BA2 7AY, UK.
Department of Medicine, Princess Alexandra Hospital NHS Foundation Trust, Harlow, CM20 1QX, UK.
Cancer Chemother Pharmacol. 2022 Sep;90(3):191-205. doi: 10.1007/s00280-022-04459-7. Epub 2022 Aug 11.
In recent years, considerable progress has been made in increasing the knowledge of tumour biology and drug resistance mechanisms in urothelial cancer. Therapeutic strategies have significantly advanced with the introduction of novel approaches such as immune checkpoint inhibitors and Fibroblast Growth Factor Receptor inhibitors. However, despite these novel agents, advanced urothelial cancer is often still progressive in spite of treatment and correlates with a poor prognosis. The introduction of antibody-drug conjugates consisting of a target-specific monoclonal antibody covalently linked to a payload (cytotoxic agent) is a novel and promising therapeutic strategy. In December 2019, the US Food and Drug Administration (FDA) granted accelerated approval to the nectin-4-targeting antibody-drug conjugate, enfortumab vedotin, for the treatment of advanced or metastatic urothelial carcinomas that are refractory to both immune checkpoint inhibitors and platinum-based treatment. Heavily pre-treated urothelial cancer patients reported a significant, 40% response to enfortumab vedotin while other antibody-drug conjugates are currently still under investigation in several clinical trials. We have comprehensively reviewed the available treatment strategies for advanced urothelial carcinoma and outlined the mechanism of action of antibody-drug conjugate agents, their clinical applications, resistance mechanisms and future strategies for urothelial cancer.
近年来,人们对膀胱癌的肿瘤生物学和耐药机制有了更深入的了解,并取得了相当大的进展。随着免疫检查点抑制剂和成纤维细胞生长因子受体抑制剂等新方法的引入,治疗策略有了显著的进步。然而,尽管有了这些新的药物,晚期膀胱癌在治疗后仍常常进展,并与预后不良相关。抗体药物偶联物的出现是一种新的、有前途的治疗策略,它由与有效载荷(细胞毒性剂)共价连接的靶向特异性单克隆抗体组成。2019 年 12 月,美国食品和药物管理局(FDA)加速批准了一种针对 nectin-4 的抗体药物偶联物——恩妥昔单抗 vedotin,用于治疗对免疫检查点抑制剂和铂类药物治疗均耐药的晚期或转移性膀胱癌。在几项临床试验中,其他抗体药物偶联物仍在研究中,而接受过大量治疗的膀胱癌患者对恩妥昔单抗 vedotin 的反应率高达 40%。我们全面回顾了晚期膀胱癌的现有治疗策略,并概述了抗体药物偶联物的作用机制、临床应用、耐药机制以及膀胱癌的未来治疗策略。