Dartford and Gravesham NHS Trust, Dartford.
Specialist Centre for Kidney Cancer, Royal Free London NHS Foundation Trust.
Curr Opin Urol. 2021 May 1;31(3):262-269. doi: 10.1097/MOU.0000000000000868.
Immune checkpoint inhibitor (ICI) combination therapy has revolutionized therapy of metastatic renal cancer. The success of immunotherapy has renewed an interest to study these agents in adjuvant and neoadjuvant settings and prior to cytoreductive nephrectomy. This narrative review will give an overview of ongoing trials and early translational research outcomes.
In nonmetastatic renal cell carcinoma (RCC), five phase 3 adjuvant and neoadjuvant trials with ICI monotherapy or combinations are ongoing with atezolizumab (IMmotion 010; NCT03024996), pembrolizumab (KEYNOTE-564; NCT03142334), nivolumab (PROSPER; NCT03055013), nivolumab with or without ipilimumab (CheckMate 914; NCT03138512) and durvalumab with or without tremelimumab (RAMPART; NCT03288532). Phase 1b/2 neoadjuvant trials demonstrate safety, efficacy and dynamic changes of immune infiltrates and provide rationales for neoadjuvant trial concepts as well as prediction of response to therapy. In primary metastatic RCC, two phase 3 trials investigate the role of deferred cytoreductive nephrectomy following pretreatment with ICI combination (NORDICSUN; NCT03977571 and PROBE; NCT04510597).
The outcomes of the major phase 3 trials are awaited as early as 2023. Meanwhile, translational data from phase 1b/2 studies enhance our understanding of the tumour immune microenvironment and its dynamic changes.
免疫检查点抑制剂(ICI)联合治疗彻底改变了转移性肾细胞癌的治疗模式。免疫治疗的成功重新激发了人们在辅助和新辅助环境以及细胞减灭性肾切除术前研究这些药物的兴趣。本文将概述正在进行的临床试验和早期转化研究结果。
在非转移性肾细胞癌(RCC)中,正在进行五项ICI 单药或联合新辅助和辅助治疗的 3 期临床试验,包括阿替利珠单抗(IMmotion 010;NCT03024996)、帕博利珠单抗(KEYNOTE-564;NCT03142334)、纳武利尤单抗(PROSPER;NCT03055013)、纳武利尤单抗联合或不联合伊匹单抗(CheckMate 914;NCT03138512)和度伐利尤单抗联合或不联合替西木单抗(RAMPART;NCT03288532)。1b/2 期的新辅助临床试验显示了安全性、疗效和免疫浸润的动态变化,并为新辅助试验概念以及预测对治疗的反应提供了依据。在原发性转移性 RCC 中,两项 3 期试验研究了 ICI 联合预处理后延迟细胞减灭性肾切除术的作用(NORDICSUN;NCT03977571 和 PROBE;NCT04510597)。
主要 3 期试验的结果最早将于 2023 年公布。与此同时,来自 1b/2 期研究的转化数据增强了我们对肿瘤免疫微环境及其动态变化的理解。