Department of Biostatistics and Computing, Yonsei University College of Medicine, Seoul, South Korea; Songdang Institute for Cancer Research, Yonsei University College of Medicine, Seoul, South Korea.
Department of Preventive Medicine, Yonsei University College of Medicine, Seoul, South Korea.
Eur J Cancer. 2021 Feb;144:49-60. doi: 10.1016/j.ejca.2020.10.030. Epub 2020 Dec 15.
The most effective agent for the third-line treatment of advanced/metastatic gastric cancer (AGC) has not yet been determined. The aim of this network meta-analysis is to compare the relative efficacy and tolerability of third-line treatments for AGC.
We conducted a comprehensive literature review of randomised clinical trials (RCTs) using four electronic databases. Overall survival (OS), progression-free survival (PFS), objective response rate (ORR) and adverse events (AEs) were used as efficacy or tolerability outcomes. A Bayesian network meta-analysis with a random-effects model was used.
Seven RCTs involving 2601 patients and nine treatments were included. The results suggested that 1 mg/kg nivolumab (nivolumab1) + 3 mg/kg ipilimumab (ipilimumab3) (hazard ratio [HR] 0.59, 95% credible interval [Crl] 0.38-0.91) was the most effective treatment, followed by nivolumab (HR 0.63, 95% Crl 0.50-0.79), for prolonging OS. Regorafenib (HR 0.40, 95% Crl 0.28-0.58) was most likely to improve PFS, followed by apatinib (HR 0.45, 95% Crl 0.33-0.60). Nivolumab1 + ipilimumab3 and nivolumab were better at improving ORR, whereas nivolumab1 + ipilimumab3 had the highest toxicity based on the AEs. For benefit-risk ratio, nivolumab, apatinib or regorafenib appeared to be the best options. Chemotherapy or two different dose combinations of nivolumab and ipilimumab were ranked as the next options because of poor tolerability, despite good efficacy.
Immunotherapy (nivolumab) or antiangiogenic agents (regorafenib and apatinib) are associated with benefits for benefit-risk ratio as third-line monotherapy. This study might serve as a guideline to aid in the selection of third-line treatments for AGC.
目前尚未确定晚期/转移性胃癌(AGC)三线治疗的最有效药物。本网络荟萃分析旨在比较 AGC 三线治疗的相对疗效和耐受性。
我们对四个电子数据库中的随机临床试验(RCT)进行了全面文献检索。总生存期(OS)、无进展生存期(PFS)、客观缓解率(ORR)和不良事件(AEs)被用作疗效或耐受性结局。使用具有随机效应模型的贝叶斯网络荟萃分析。
纳入 7 项 RCT,共 2601 例患者,涉及 9 种治疗方案。结果表明,1mg/kg 纳武利尤单抗(nivolumab1)+3mg/kg 伊匹单抗(ipilimumab3)(风险比[HR]0.59,95%可信区间[Crl]0.38-0.91)是延长 OS 最有效的治疗方法,其次是纳武利尤单抗(HR 0.63,95% Crl 0.50-0.79)。regorafenib(HR 0.40,95% Crl 0.28-0.58)最有可能改善 PFS,其次是阿帕替尼(HR 0.45,95% Crl 0.33-0.60)。nivolumab1+ipilimumab3 和 nivolumab 改善 ORR 的效果更好,而 nivolumab1+ipilimumab3 基于 AEs 的毒性最高。基于获益-风险比,nivolumab、阿帕替尼或 regorafenib 似乎是最佳选择。由于耐受性差,尽管疗效良好,但化疗或两种不同剂量的 nivolumab 和 ipilimumab 联合治疗被列为下一个选择。
免疫治疗(nivolumab)或抗血管生成药物(regorafenib 和阿帕替尼)作为三线单药治疗与获益-风险比相关。本研究可为 AGC 的三线治疗选择提供指导。