PD-1/L1 inhibitors can improve but not replace chemotherapy for advanced urothelial carcinoma: A systematic review and network meta-analysis

Cancer Innovation Pub Date : 2023-05-19 DOI:10.1002/cai2.75
Longkun Mao, Meihua Yang, Xinxiang Fan, Wenjie Li, Xiaodong Huang, Wang He, Tianxin Lin, Jian Huang
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Abstract

Background

Programmed cell death-1/ligand 1 inhibitors are a new treatment strategy for advanced urothelial carcinoma. Therefore, a comparative evaluation of their efficacy and toxicity compared with chemotherapy is necessary.

Methods

We comprehensively searched PubMed, Web of Science, Embase, and Cochrane Library databases and performed a meta-analysis of randomized controlled trials up to July 2021. We considered overall survival as the primary outcome, and progression-free survival, objective response rate, and treatment-related adverse events as secondary outcomes.

Results

Overall, 3584 patients from five studies were evaluated. Compared with first-line chemotherapy, programmed cell death-1/ligand 1 inhibitors were significantly associated with worse progression-free survival (p < 0.001) and adverse objective response rates (p < 0.001). However, the treatments were not significantly different in terms of overall survival (p = 0.33). Compared with second-line chemotherapy, programmed cell death-1/ligand 1 inhibitors significantly improved overall survival (p < 0.001), and there was no statistically significant difference in progression-free survival (p = 0.89) or objective response rate (p = 0.34). Compared with chemotherapy, programmed cell death-1/ligand 1 inhibitors were well tolerated (first-line chemotherapy: p < 0.001; second-line chemotherapy: p < 0.001).

Conclusions

The efficacy of programmed cell death-1/ligand 1 inhibitors in patients with advanced urothelial carcinoma is not superior to that of first-line platinum-based chemotherapy but is better than second-line chemotherapy; however, programmed cell death-1/ligand 1 inhibitors are safer than first- and second-line chemotherapy and have a broader prospect for use in combination therapy.

Abstract Image

PD-1/L1抑制剂可以改善但不能取代晚期尿路上皮癌的化疗:一项系统综述和网络荟萃分析
背景程序性细胞死亡-1/配体1抑制剂是晚期尿路上皮癌的一种新的治疗策略。因此,与化疗相比,有必要对其疗效和毒性进行比较评估。方法我们全面搜索PubMed、Web of Science、Embase和Cochrane Library数据库,并对截至2021年7月的随机对照试验进行荟萃分析。我们认为总生存率是主要结果,无进展生存率、客观缓解率和治疗相关不良事件是次要结果。结果总共对来自5项研究的3584名患者进行了评估。与一线化疗相比,程序性细胞死亡-1/配体1抑制剂与较差的无进展生存率显著相关(p <; 0.001)和不良客观反应率(p <; 0.001)。然而,就总生存率而言,两种治疗没有显著差异(p = 0.33)。与二线化疗相比,程序性细胞死亡-1/配体1抑制剂显著提高了总生存率(p <; 0.001),并且在无进展生存率方面没有统计学上的显著差异(p = 0.89)或客观应答率(p = 0.34)。与化疗相比,程序性细胞死亡-1/配体1抑制剂耐受性良好(一线化疗:p <; 0.001;二线化疗:p <; 0.001)。结论程序性细胞死亡-1/配体1抑制剂治疗晚期尿路上皮癌的疗效并不优于一线铂类化疗,但优于二线化疗;然而,程序性细胞死亡-1/配体1抑制剂比一线和二线化疗更安全,在联合治疗中有更广阔的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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