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程序性死亡 1 和程序性死亡配体 1 抑制剂在晚期和复发性尿路上皮癌中的应用:单药研究的荟萃分析。

Programmed Death 1 and Programmed Death Ligand 1 Inhibitors in Advanced and Recurrent Urothelial Carcinoma: Meta-analysis of Single-Agent Studies.

机构信息

USC Institute of Urology and Catherine & Joseph Aresty Department of Urology, University of Southern California, Keck School of Medicine, Los Angeles, CA; Department of Urology, University of Verona, Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.

Biostatistics Division, Mercy Lab Foundation, Irvine, CA.

出版信息

Clin Genitourin Cancer. 2020 Oct;18(5):351-360.e3. doi: 10.1016/j.clgc.2020.01.004. Epub 2020 Jan 31.

Abstract

We performed a systematic review and meta-analysis on the response rates of patients with treatment-refractory urothelial carcinoma treated with programmed cell death 1 (PD-1) and programmed death ligand 1 (PD-L1) inhibitors. We reviewed the literature for prospective studies evaluating PD-1/PD-L1 inhibitors in refractory urothelial carcinoma patients, which formed the basis for US Food and Drug Administration approval of 5 different antagonistic antibodies targeting PD-1 or PD-L1 (atezolizumab, durvalumab, avelumab, nivolumab, and pembrolizumab). We considered studies examining PD-1/PD-L1-treated patients, which we identified using the following key terms in the Pubmed, Scopus, Web of Science, ClinicalTrial.gov, and Cochrane Library databases. Eligible studies had ≥ 20 patients each and reported response rates, duration of response, and overall survival (OS). We performed fixed and random-effects meta-analyses to model the point estimates for objective response rate and complete response. The median progression-free survival (PFS) and OS for studies reporting these statistics were evaluated. We found 10 eligible studies that met our inclusion criteria, providing extractable numerators and denominators for response rates, PFS, and OS for 1934 patients with metastatic urothelial carcinoma. The objective response rate was 18% (95% confidence interval, 15-22) for second-line or later therapies. The random-effects estimate for complete response was 4% (95% confidence interval, 3-5), including all disease locations and all PD-1 and PD-L1 inhibitors. Median OS and PFS were < 13 months and 3 months, respectively, across all studies, irrespective of PD-L1 expression. We found that the estimated response rates of agents included in this meta-analysis seem to be more favorable than other salvage therapies.

摘要

我们对治疗难治性尿路上皮癌患者的程序性细胞死亡 1(PD-1)和程序性死亡配体 1(PD-L1)抑制剂的反应率进行了系统评价和荟萃分析。我们查阅了评估 PD-1/PD-L1 抑制剂在难治性尿路上皮癌患者中的前瞻性研究文献,这些研究为美国食品和药物管理局批准 5 种不同的针对 PD-1 或 PD-L1 的拮抗抗体提供了依据(阿替利珠单抗、度伐利尤单抗、avelumab、纳武利尤单抗和帕博利珠单抗)。我们考虑了使用 Pubmed、Scopus、Web of Science、ClinicalTrial.gov 和 Cochrane Library 数据库中的以下关键词来检查接受 PD-1/PD-L1 治疗的患者的研究。合格的研究每个研究都有≥20 名患者,并报告了反应率、反应持续时间和总生存期(OS)。我们进行了固定效应和随机效应荟萃分析,以对客观反应率和完全缓解的点估计进行建模。评估了报告这些统计数据的研究的中位无进展生存期(PFS)和 OS。我们发现了 10 项符合纳入标准的合格研究,为 1934 名转移性尿路上皮癌患者提供了可提取的反应率、PFS 和 OS 的分子和分母。二线或二线以上治疗的客观反应率为 18%(95%置信区间,15-22)。包括所有疾病部位和所有 PD-1 和 PD-L1 抑制剂的完全缓解的随机效应估计值为 4%(95%置信区间,3-5)。无论 PD-L1 表达如何,所有研究的中位 OS 和 PFS 均<13 个月和 3 个月。我们发现,纳入本荟萃分析的药物的估计反应率似乎比其他挽救疗法更有利。

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