Liu Linfeng, Chen Dengzhuo, Wen Liang, Ma Yongli, Li Jinghui, Zhang Guosheng, Hu Hongkai, Huang Chengzhi, Yao Xueqing
Gannan Medical University, Ganzhou, China.
Ganzhou Hospital of Guangdong Provincial People's Hospital, Ganzhou Municipal Hospital, Ganzhou, China.
Expert Rev Anticancer Ther. 2025 Apr;25(4):411-421. doi: 10.1080/14737140.2025.2474736. Epub 2025 Mar 6.
Fruquintinib, a VEGFR1-3 tyrosine kinase inhibitor, is approved for treating refractory metastatic colorectal cancer. Recent clinical practice has shown that combining fruquintinib with programmed cell death protein 1 (PD-1) inhibitors can achieve better efficacy.The objective of this study is to assess the efficacy and safety of combining PD-1inhibitors with fruquintinib.
We systematically searched PubMed, Cochrane Library, Embase, Wanfang, and CNKI up to 28 August 2024 for studies comparing fruquintinib combined with PD-1 inhibitors to fruquintinib alone. RevMan software was used to perform meta-analyses of survival data for the included studies.
A total of 9 retrospective cohort studies and 1 randomized controlled trial were included, involving a total of 716 patients. Compared with the monotherapy group, the combination therapy group had a greater Overall Response Rate [RR = 2.45,95% CI (1.83, 3.56), < 0.00001], Disease Control Rate [RR = 1.37,95% CI (1.64,4.79), = 0.0002], and progression-free survival [HR = 0.64,95% CI (0.49, 0.84), = 0.001]. However, there was no significant difference in overall survival between the two groups. The incidence of adverse effects was identical in both groups.
Fruquintinib combined with PD-1 inhibitors was more effective than fruquintinib alone in the treatment of advanced colorectal cancer, with acceptable safety.
PROSPERO (registration number CRD42024583116).
呋喹替尼是一种血管内皮生长因子受体1-3(VEGFR1-3)酪氨酸激酶抑制剂,已被批准用于治疗难治性转移性结直肠癌。近期临床实践表明,将呋喹替尼与程序性细胞死亡蛋白1(PD-1)抑制剂联合使用可取得更好的疗效。本研究的目的是评估PD-1抑制剂与呋喹替尼联合使用的疗效和安全性。
我们系统检索了截至2024年8月28日的PubMed、Cochrane图书馆、Embase、万方和中国知网,以查找比较呋喹替尼联合PD-1抑制剂与单用呋喹替尼的研究。使用RevMan软件对纳入研究的生存数据进行荟萃分析。
共纳入9项回顾性队列研究和1项随机对照试验,涉及716例患者。与单药治疗组相比,联合治疗组的总缓解率更高[风险比(RR)=2.45,95%置信区间(CI)(1.83,3.56),P<0.00001]、疾病控制率更高[RR=1.37,95%CI(1.64,4.79),P=0.0002]和无进展生存期更长[风险比(HR)=0.64,95%CI(0.49,0.84),P=0.001]。然而,两组的总生存期无显著差异。两组的不良反应发生率相同。
在治疗晚期结直肠癌方面,呋喹替尼联合PD-1抑制剂比单用呋喹替尼更有效,且安全性可接受。
国际前瞻性系统评价注册库(PROSPERO)(注册号CRD42024583116)