Division of Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Italy.
Division of Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Italy.
Eur Urol Focus. 2022 Jan;8(1):152-159. doi: 10.1016/j.euf.2021.01.003. Epub 2021 Jan 27.
Immune checkpoint inhibitors (ICIs) have reported durable responses in selected groups of patients with metastatic urothelial carcinoma (mUC). However, identification of biomarkers predictive of response to ICIs remains an unmet need in mUC management, and the role of programmed cell death ligand 1 (PD-L1) expression remains controversial.
In this systematic review and meta-analysis, we aimed at assessing the predictive value of PD-L1 in mUC patients receiving first-line ICIs as monotherapy or in combination with other anticancer agents across randomized controlled clinical trials (RCTs).
We retrieved all the relevant RCTs through PubMed/Medline, Cochrane library, and EMBASE; proceedings of the main international oncological meetings were also searched for relevant abstracts. Eligible studies included RCTs evaluating ICIs versus chemotherapy in PD-L1-positive mUCs; the primary endpoint was overall survival (OS).
Three phase III trials matched our eligibility criteria; a total of 2237 PD-L1-positive mUC patients (ICIs: 1125; chemotherapy: 1112) were included in the analysis. Compared with chemotherapy, ICIs were associated with higher OS in PD-L1-positive patients (hazard ratio [HR] 0.86, 95% confidence interval [CI] 0.78-0.96; p = 0.007); conversely, no differences were observed in the PD-L1-negative patient population (HR 1.03, 95% CI 0.89-1.19; p < 0.001).
Compared with standard chemotherapy, our results suggested a survival benefit in PD-L1-positive mUC patients receiving ICIs; conversely, no benefit was observed in patients with PD-L1-negative disease. Although this systematic review and meta-analysis should be interpreted with caution due to several issues, our results highlight the need for reliable predictive biomarkers of response to ICIs, providing a benchmark for future studies in this setting.
Despite immune checkpoint inhibitors (ICIs) having revolutionized the treatment landscape of metastatic urothelial carcinoma (mUC), an important percentage of patients do not experience clinical benefit or durable responses. Identification of reliable biomarkers of response to ICIs remains a mandatory need in mUC management, and further efforts are needed to standardize the assessment of programmed cell death ligand 1 in urothelial carcinoma.
免疫检查点抑制剂(ICIs)在转移性尿路上皮癌(mUC)的某些患者群体中报告了持久的反应。然而,在 mUC 管理中,识别预测对 ICI 反应的生物标志物仍然是一个未满足的需求,而程序性死亡配体 1(PD-L1)表达的作用仍然存在争议。
在这项系统评价和荟萃分析中,我们旨在评估 PD-L1 在接受一线 ICI 单药治疗或与其他抗癌药物联合治疗的 mUC 患者中的预测价值,这些患者来自随机对照临床试验(RCTs)。
我们通过 PubMed/Medline、Cochrane 图书馆和 EMBASE 检索了所有相关的 RCTs;还搜索了主要国际肿瘤学会议的会议记录,以获取相关摘要。符合条件的研究包括评估 PD-L1 阳性 mUC 中 ICI 与化疗的 RCT;主要终点是总生存期(OS)。
三项 III 期试验符合我们的入选标准;共纳入 2237 例 PD-L1 阳性 mUC 患者(ICI:1125;化疗:1112)进行分析。与化疗相比,ICI 在 PD-L1 阳性患者中与更高的 OS 相关(风险比 [HR] 0.86,95%置信区间 [CI] 0.78-0.96;p = 0.007);然而,在 PD-L1 阴性患者人群中未观察到差异(HR 1.03,95% CI 0.89-1.19;p < 0.001)。
与标准化疗相比,我们的结果表明,接受 ICI 治疗的 PD-L1 阳性 mUC 患者有生存获益;相反,PD-L1 阴性疾病患者未观察到获益。尽管由于存在几个问题,本系统评价和荟萃分析的结果应谨慎解释,但我们的结果强调了需要可靠的预测生物标志物来预测对 ICI 的反应,为该领域的未来研究提供了基准。
尽管免疫检查点抑制剂(ICIs)彻底改变了转移性尿路上皮癌(mUC)的治疗格局,但仍有相当一部分患者没有临床获益或持久反应。在 mUC 管理中,识别预测对 ICI 反应的可靠生物标志物仍然是一项强制性需求,需要进一步努力标准化在尿路上皮癌中评估程序性死亡配体 1。