Campbell Matthew T, Siefker-Radtke Arlene O, Gao Jianjun
From the Department of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX.
Cancer J. 2016 Mar-Apr;22(2):96-100. doi: 10.1097/PPO.0000000000000175.
Immune checkpoint inhibition will be the first treatment breakthrough in recurrent and metastatic urothelial carcinoma since the introduction of combination chemotherapy more than 30 years ago. Monoclonal antibodies that target cytotoxic T-lymphocyte antigen 4, programmed death receptor 1, and programmed death receptor ligand 1 are furthest along in clinical development. Specific antibodies targeting either programmed death receptor 1 or programmed death receptor ligand 1 have demonstrated significant single-agent activity with impressive safety and tolerability for heavily pretreated patients in early-phase clinical trials. In our review, we discuss the rationale for immunotherapy in urothelial cancer, completed and ongoing studies with immune checkpoint therapy, the development of molecular subtypes of urothelial carcinoma with the potential impact of immunotherapy in these new groupings, and future directions of exploration with these agents in both early- and late-stage disease.
自30多年前联合化疗引入以来,免疫检查点抑制将成为复发性和转移性尿路上皮癌的首个治疗突破。靶向细胞毒性T淋巴细胞抗原4、程序性死亡受体1和程序性死亡受体配体1的单克隆抗体在临床开发方面进展最为显著。在早期临床试验中,针对程序性死亡受体1或程序性死亡受体配体1的特异性抗体已显示出显著的单药活性,对经过大量预处理的患者具有令人印象深刻的安全性和耐受性。在本综述中,我们讨论了尿路上皮癌免疫治疗的基本原理、免疫检查点治疗的已完成和正在进行的研究、尿路上皮癌分子亚型的发展以及免疫治疗在这些新分类中的潜在影响,以及这些药物在早期和晚期疾病中的未来探索方向。