Immunotherapy Plus Chemotherapy Versus Chemotherapy Alone as First-Line Treatment for Advanced Urothelial Cancer: An Updated Systematic Review and Meta-Analysis of Randomized Controlled Trials
Isadora Mamede , Lorena Escalante-Romero , Davi S. Gonçalves Celso , Pedro C. Abrahao Reis , Maria Inez Dacoregio , Ana Caroline Alves , Carlos Stecca
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引用次数: 0
Abstract
Introduction
Platinum-based chemotherapy (CTX) has historically been the primary treatment for advanced urothelial cancer (aUC), with limited alternative options. The therapeutic landscape experienced a paradigm shift following the results of the EV-302 and Checkmate-901 trials, which led to the approval of Enfortumab vedotin plus pembrolizumab (EV-P) as the preferred first-line treatment, and nivolumab plus CTX for those unable to receive the preferred regimen. Currently, further investigations are underway to explore PD-1 and PD-L1 inhibitors in the initial treatment of aUC.
Patients and methods
We conducted a systematic search across PubMed, Embase, and the Cochrane Library for randomized controlled trials (RCTs) comparing immune checkpoint inhibitors (ICI)-CTX combinations versus CTX alone as first-line treatment for advanced UC. Employing a random-effects model, we pooled hazard ratios (HR) with 95% confidence intervals (CI).
Results
Our analysis encompassed 3 RCTs, involving 2162 participants, with 51.16% randomized to combination therapy with platinum-based CTX. Compared to CTX alone, immune-chemotherapy significantly improved overall survival (HR 0.84; 95% CI 0.75-0.93; P < .01), progression-free survival (HR 0.78; 95% CI 0.70-0.86; P < .01), and objective response rate (RR 1.20; 95% CI 1.06-1.36; P < .01), while elevating the risk of immune-related adverse events (P-value = .02).
Conclusion
In this meta-analysis of RCTs, ICI plus CTX demonstrated a significant association with improved survival at the expense of an increased risk of immune-related adverse events. Therefore, our findings suggest that this combination should be considered as an initial treatment for aUC in platinum-eligible patients who cannot receive EV-P.
导言铂类化疗(CTX)历来是晚期尿路上皮癌(aUC)的主要治疗方法,替代方案有限。在EV-302和Checkmate-901试验结果公布后,治疗模式发生了转变,Enfortumab vedotin加pembrolizumab(EV-P)被批准为首选一线治疗方案,nivolumab加CTX被批准用于无法接受首选方案的患者。患者和方法我们在PubMed、Embase和Cochrane图书馆对随机对照试验(RCT)进行了系统性检索,比较了免疫检查点抑制剂(ICI)-CTX联合治疗与单用CTX作为晚期UC一线治疗的效果。采用随机效应模型,我们汇总了危险比(HR)及95%置信区间(CI)。结果我们的分析包括3项RCT,涉及2162名参与者,其中51.16%的参与者随机接受了铂类CTX联合疗法。与单用CTX相比,免疫化疗能显著提高总生存期(HR 0.84; 95% CI 0.75-0.93; P <.01)、无进展生存期(HR 0.78; 95% CI 0.70-0.86; P <.01)和客观反应率(RR 1.20; 95% CI 1.06-1.36; P <.01)。结论在这项RCT荟萃分析中,ICI加CTX与生存率改善有显著相关性,但以免疫相关不良事件风险增加为代价。因此,我们的研究结果表明,对于符合铂治疗条件但无法接受EV-P治疗的患者,应考虑将这种联合疗法作为aUC的初始治疗方法。
期刊介绍:
Clinical Genitourinary Cancer is a peer-reviewed journal that publishes original articles describing various aspects of clinical and translational research in genitourinary cancers. Clinical Genitourinary Cancer is devoted to articles on detection, diagnosis, prevention, and treatment of genitourinary cancers. The main emphasis is on recent scientific developments in all areas related to genitourinary malignancies. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.