Department of Neurology, Shandong Provincial Third Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Shandong Provincial Third Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Front Immunol. 2024 Nov 1;15:1485303. doi: 10.3389/fimmu.2024.1485303. eCollection 2024.
The efficacy and safety of PD-1/PD-L1 inhibitors combined with CTLA-4 inhibitors in the treatment of advanced colorectal cancer is controversial. This meta-analysis aimed to evaluate the efficacy and safety of PD-1/PD-L1 inhibitors combined with CTLA-4 inhibitors for advanced colorectal cancer.
PubMed, Embase, the Cochrane Library, and Web of Science databases were systematically searched for relevant studies. Outcomes including median progression-free survival (mPFS), median overall survival (mOS), overall response rate (ORR), disease control rate (DCR), treatment-related adverse events (TRAEs) and ≥grade 3 TRAEs were extracted for further analysis. The risk of bias was assessed by subgroup analysis.
12 articles with 566 patients were identified and subjected to meta-analysis. With regard to survival analysis, the pooled mOS and mPFS were 6.66 months (95%CI 4.85-9.16) and 2.92 months (95%CI 2.23-3.83), respectively. In terms of tumor response, the pooled ORR and DCR were 21% (95%CI 6%-41%) and 49% (95%CI 27%-71%), respectively. The pooled AEs rate and ≥ grade 3 AEs rate were 94% (95%CI 86%-99%) and 44% (95%CI 30%-58%).
PD-1/PD-L1 inhibitors combined with CTLA-4 inhibitors have shown promising clinical responses in the treatment of colorectal cancer (CRC). Although the incidence of adverse reactions is high, they are generally tolerable.
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PD-1/PD-L1 抑制剂联合 CTLA-4 抑制剂治疗晚期结直肠癌的疗效和安全性存在争议。本荟萃分析旨在评估 PD-1/PD-L1 抑制剂联合 CTLA-4 抑制剂治疗晚期结直肠癌的疗效和安全性。
系统检索 PubMed、Embase、Cochrane 图书馆和 Web of Science 数据库中相关研究。提取中位无进展生存期(mPFS)、中位总生存期(mOS)、总缓解率(ORR)、疾病控制率(DCR)、治疗相关不良事件(TRAEs)和≥3 级 TRAEs 等结局指标进行荟萃分析。采用亚组分析评估偏倚风险。
共纳入 12 篇文献 566 例患者,进行荟萃分析。生存分析结果显示,mOS 和 mPFS 分别为 6.66 个月(95%CI 4.85-9.16)和 2.92 个月(95%CI 2.23-3.83)。肿瘤反应方面,ORR 和 DCR 分别为 21%(95%CI 6%-41%)和 49%(95%CI 27%-71%)。TRAEs 发生率和≥3 级 TRAEs 发生率分别为 94%(95%CI 86%-99%)和 44%(95%CI 30%-58%)。
PD-1/PD-L1 抑制剂联合 CTLA-4 抑制剂治疗结直肠癌具有良好的临床疗效,但不良反应发生率较高,多为可耐受。
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