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免疫疗法在晚期尿路上皮癌中的新作用。

Emerging Role of Immunotherapy in Advanced Urothelial Carcinoma.

机构信息

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.

出版信息

Curr Oncol Rep. 2018 Apr 11;20(6):48. doi: 10.1007/s11912-018-0693-y.

Abstract

PURPOSE OF REVIEW

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.

RECENT FINDINGS

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.

摘要

目的综述

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。

最新发现

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。

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