Department of Radiation Oncology, Yantai Affiliated Hospital of Binzhou Medical University, No 717, Jinbu Road, Yantai, 264000, Shandong, China.
Department of Respiratory, Yantai Affiliated Hospital of Binzhou Medical University, Yantai, 264000, China.
Eur J Med Res. 2023 Aug 27;28(1):302. doi: 10.1186/s40001-023-01272-7.
Previous studies showed that the combination of bevacizumab and erlotinib (combination therapy) significantly prolonged progression-free survival (PFS) but no overall survival (OS) compared to erlotinib alone (monotherapy) for advanced EGFR-mutant non-small cell lung cancer (NSCLC). Two phase III randomized controlled trials (RCTs) had reported the OS results in 2021. This meta-analysis aimed to include the results of the two RCTs to make a decision.
We systematically searched relevant databases for RCTs on the use of bevacizumab plus erlotinib in advanced EGFR-mutant NSCLC. The main outcomes of interest were PFS, OS, and the reported hazard ratio (HR). Fixed-effect model was used to estimate pooled HR.
Total 5 RCTs with 935 patients were eligible for this meta-analysis. All studies reached their primary study endpoints including PFS and OS. Compared to monotherapy, combination therapy remarkably prolonged PFS (HR = 0.60, 95% confidence interval CI 0.51-0.70; p < 0.00001); however, OS was similar between the two groups (HR = 0.90, 95% CI 0.76-1.08; p = 0.26). Subgroup analysis demonstrated that in deletion within exon 19 (19del) mutation subgroup, the combination therapy could only prolong PFS (HR = 0.60, 95% CI 0.47-0.76; p < 0.0001) but not OS (HR = 1.00, 95% CI 0.73-1.37; p = 1.00), and also in leucine-to-arginine substitution in exon 21 (L858R) mutation subgroup (HR = 0.59, p < 0.0001 and HR = 0.80, p = 0.18, respectively). For patients with brain metastasis at baseline, the combination therapy achieved a significant better PFS than the monotherapy (HR = 0.60, 95% CI 0.39-0.90; p = 0.01), and a better OS with the difference marginally significant (HR = 0.69, 95% CI 0.46-1.02; p = 0.06).
Combination of bevacizumab and erlotinib can prolong progression-free survival but not overall survival compared to erlotinib alone in advanced EGFR-mutant non-small cell lung cancer patients. The combination therapy not only can prolong progression-free survival but also has a tendency to prolong overall survival for patients with brain metastasis at baseline.
先前的研究表明,贝伐珠单抗联合厄洛替尼(联合治疗)与厄洛替尼单药治疗(单药治疗)相比,显著延长了晚期 EGFR 突变非小细胞肺癌(NSCLC)患者的无进展生存期(PFS),但未延长总生存期(OS)。两项 III 期随机对照试验(RCT)在 2021 年报告了 OS 结果。本荟萃分析旨在纳入这两项 RCT 的结果以做出决策。
我们系统地检索了有关贝伐珠单抗联合厄洛替尼治疗晚期 EGFR 突变 NSCLC 的 RCT 相关数据库。主要观察终点为 PFS、OS 和报告的风险比(HR)。采用固定效应模型估计汇总 HR。
共有 5 项 RCT 共 935 例患者符合本荟萃分析纳入标准。所有研究均达到了 PFS 和 OS 的主要研究终点。与单药治疗相比,联合治疗显著延长了 PFS(HR=0.60,95%置信区间 CI 0.51-0.70;p<0.00001);然而,两组之间的 OS 无显著差异(HR=0.90,95%置信区间 CI 0.76-1.08;p=0.26)。亚组分析表明,在缺失 19 号外显子(19del)突变亚组中,联合治疗仅能延长 PFS(HR=0.60,95%置信区间 CI 0.47-0.76;p<0.0001),但不能延长 OS(HR=1.00,95%置信区间 CI 0.73-1.37;p=1.00),在 21 号外显子亮氨酸到精氨酸取代(L858R)突变亚组中也有同样的结果(HR=0.59,p<0.0001 和 HR=0.80,p=0.18)。对于基线时有脑转移的患者,联合治疗在 PFS 方面明显优于单药治疗(HR=0.60,95%置信区间 CI 0.39-0.90;p=0.01),OS 也有更好的趋势,但差异无统计学意义(HR=0.69,95%置信区间 CI 0.46-1.02;p=0.06)。
贝伐珠单抗联合厄洛替尼与厄洛替尼单药治疗相比,可延长晚期 EGFR 突变非小细胞肺癌患者的无进展生存期,但不能延长总生存期。对于基线时有脑转移的患者,联合治疗不仅能延长无进展生存期,而且有延长总生存期的趋势。