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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Currently, further investigations are underway to explore PD-1 and PD-L1 inhibitors in the initial treatment of aUC.</p></div><div><h3>Patients and methods</h3><p>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).</p></div><div><h3>Results</h3><p>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; <em>P</em> < .01), progression-free survival (HR 0.78; 95% CI 0.70-0.86; <em>P</em> < .01), and objective response rate (RR 1.20; 95% CI 1.06-1.36; <em>P</em> < .01), while elevating the risk of immune-related adverse events (<em>P</em>-value = .02).</p></div><div><h3>Conclusion</h3><p>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.</p></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"Isadora Mamede , Lorena Escalante-Romero , Davi S. Gonçalves Celso , Pedro C. Abrahao Reis , Maria Inez Dacoregio , Ana Caroline Alves , Carlos Stecca\",\"doi\":\"10.1016/j.clgc.2024.102154\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>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.</p></div><div><h3>Patients and methods</h3><p>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).</p></div><div><h3>Results</h3><p>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; <em>P</em> < .01), progression-free survival (HR 0.78; 95% CI 0.70-0.86; <em>P</em> < .01), and objective response rate (RR 1.20; 95% CI 1.06-1.36; <em>P</em> < .01), while elevating the risk of immune-related adverse events (<em>P</em>-value = .02).</p></div><div><h3>Conclusion</h3><p>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.</p></div>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-07-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1558767324001253\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1558767324001253","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
摘要
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。
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
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.