Cleveland Clinic Taussig Cancer Institute, 9500 Euclid Ave, Desk CA-60, Cleveland, OH, 44195, USA.
Department of Medicine, Division of Oncology, Seattle Cancer Care Alliance, University of Washington and Fred Hutchinson Cancer Research Center, 825 Eastlake Ave E, MS: G4-830, Seattle, WA, 98109, USA.
Curr Oncol Rep. 2018 Apr 11;20(6):48. doi: 10.1007/s11912-018-0693-y.
Advanced urothelial carcinoma (aUC) has long been treated preferably with cisplatin-based chemotherapy, but many patients are cisplatin-ineligible whereas for those who progress on a platinum-based regimen treatment options are limited. We review key recent data regarding immune checkpoint inhibitors that are changing this treatment landscape.
Since May 2016, five different agents targeting the PD-1/PD-L1 pathway (atezolizumab, pembrolizumab, nivolumab, avelumab, durvalumab) have received FDA approval for the treatment of aUC in the platinum-refractory setting, while pembrolizumab and atezolizumab are FDA-approved for cisplatin-ineligible patients in the first-line setting. Clinical outcomes and safety profiles of these agents appear relatively comparable across separate trials; however, only pembrolizumab is supported by level I evidence from a large randomized phase III trial showing overall survival benefit over conventional cytotoxic salvage chemotherapy in the platinum-refractory setting. Pembrolizumab has the highest level of evidence in platinum-refractory aUC, whereas pembrolizumab and atezolizumab have comparable level of evidence in the frontline setting in cisplatin-ineligible patients. Ongoing research is evaluating novel agents, various rational combinations, and sequences, as well as predictive and prognostic biomarkers.
高级尿路上皮癌(aUC)长期以来一直首选顺铂为基础的化疗治疗,但许多患者不能耐受顺铂,而对于那些在铂类方案治疗后进展的患者,治疗选择有限。我们综述了关于免疫检查点抑制剂的最新关键数据,这些数据正在改变这一治疗格局。
自 2016 年 5 月以来,五种不同的靶向 PD-1/PD-L1 通路的药物(阿替利珠单抗、帕博利珠单抗、纳武利尤单抗、avelumab、度伐利尤单抗)已获得 FDA 批准,用于铂类耐药患者的 aUC 治疗,而帕博利珠单抗和阿替利珠单抗则被 FDA 批准用于铂类不耐受患者的一线治疗。这些药物在单独的试验中,其临床疗效和安全性似乎相对相当;然而,只有帕博利珠单抗在一项大型随机 III 期试验中得到了一级证据的支持,该试验显示在铂类耐药患者中,总生存期优于传统细胞毒性解救化疗。帕博利珠单抗在铂类耐药的 aUC 中具有最高水平的证据,而在铂类不耐受患者的一线治疗中,帕博利珠单抗和阿替利珠单抗具有相当水平的证据。正在进行的研究正在评估新型药物、各种合理的联合用药及其顺序,以及预测和预后生物标志物。