Department of Urology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Department of Medicine, Watford General Hospital, Watford, UK.
Curr Opin Oncol. 2023 May 1;35(3):186-199. doi: 10.1097/CCO.0000000000000942. Epub 2023 Mar 14.
Bladder cancer is the 12th most common cancer worldwide. Historically, the systemic management of urothelial carcinoma has been confined to platinum-based chemotherapy. In this review, we discuss the evolving landscape of systemic treatment for urothelial carcinoma.
Since 2016, when the Food and Drug Administration approved the first immune checkpoint inhibitor (CPI), programmed cell death 1 and programmed cell death ligand 1 inhibitors have been evaluated in the nonmuscle invasive bladder cancer, localized muscle invasive bladder cancer as well as advanced/metastatic bladder cancer settings. Newer approved treatments such as fibroblast growth factor receptor (FGFR) inhibitors and antibody-drug conjugates (ADCs) represent second-line and third-line options. These novel treatments are now being assessed in combination as well as with older traditional platinum-based chemotherapy.
Novel therapies continue to improve bladder cancer outcomes. Personalized approach with well validated biomarkers are important to predict response to therapy.
膀胱癌是全球第 12 大常见癌症。从历史上看,尿路上皮癌的系统治疗仅限于铂类化疗。在这篇综述中,我们讨论了尿路上皮癌系统治疗的不断发展。
自 2016 年美国食品和药物管理局批准首个免疫检查点抑制剂(CPI)以来,程序性细胞死亡 1 和程序性细胞死亡配体 1 抑制剂已在非肌肉浸润性膀胱癌、局部肌肉浸润性膀胱癌以及晚期/转移性膀胱癌中进行了评估。新批准的治疗方法,如成纤维细胞生长因子受体(FGFR)抑制剂和抗体药物偶联物(ADC),代表二线和三线治疗选择。这些新的治疗方法现在正在联合以及与传统的铂类化疗药物进行评估。
新型疗法继续改善膀胱癌的预后。具有良好验证生物标志物的个性化方法对于预测对治疗的反应非常重要。