Department of Stomatology, Chinese People's Liberation Army General Hospital, No.28 Fuxing Road, Haidian District, Beijing, 100853, People's Republic of China.
Eur J Clin Pharmacol. 2011 Mar;67(3):235-43. doi: 10.1007/s00228-010-0965-4. Epub 2011 Jan 5.
The epidermal growth factor receptor (EGFR) is one of the four human epidermal receptors. The efficacy and safety of EGFR-targeted therapies for treating non-small-cell lung cancer (NSCLC) remained controversial. The aim of this study was to systematically evaluate EGFR-targeted therapies plus chemotherapy for advanced NSCLC.
Cochrane Central Register of Controlled Trials, PubMed, and Embase were searched for relevant studies. Quantitative analysis was carried out to evaluate survival, response, and toxicity of EGFR-targeted therapies.
Ten randomized controlled trials (RCTs) involving 5,936 patients were identified out of 107 studies. There was no statistical difference in overall (OS) and 1-year (OYS) survival rate when small-molecule tyrosine kinase inhibitors (TKIs) plus platinum-based doublet chemotherapy (PBDC) were compared with PBDC alone. However, progression-free survival [hazard ratio (HR)=0.87, 95% confidence interval (CI) 0.76-0.99] and overall response rate (ORR) were marginally improved. Prolonged OS (HR=0.87, 95% CI 0.78-0.96) and increased ORR and OYS were found when cetuximab plus PBDC was compared with PBDC alone. Adverse events in the combination arms were similar in incidence to those of the chemotherapy-alone arms, with the exception of an increased incidence of rash and diarrhea.
Cetuximab adds benefits to NSCLC patients compared with PBDC alone. Small-molecule TKIs plus PBDC lead to a slightly additive efficacy compared with PBDC alone.
表皮生长因子受体(EGFR)是人类表皮受体的四个之一。EGFR 靶向治疗非小细胞肺癌(NSCLC)的疗效和安全性仍存在争议。本研究旨在系统评估 EGFR 靶向治疗联合化疗治疗晚期 NSCLC。
检索 Cochrane 对照试验中心注册库、PubMed 和 Embase 以获取相关研究。定量分析评估了 EGFR 靶向治疗的生存、反应和毒性。
从 107 项研究中确定了 10 项随机对照试验(RCT),涉及 5936 例患者。与单独使用 PBDC 相比,小分子酪氨酸激酶抑制剂(TKI)联合铂类双药化疗(PBDC)并未改善总生存(OS)和 1 年生存率(OYS)。然而,无进展生存期[风险比(HR)=0.87,95%置信区间(CI)0.76-0.99]和总缓解率(ORR)略有改善。与单独使用 PBDC 相比,西妥昔单抗联合 PBDC 可延长 OS(HR=0.87,95% CI 0.78-0.96),并提高 ORR 和 OYS。联合治疗组的不良反应发生率与化疗组相似,除皮疹和腹泻发生率增加外。
与单独使用 PBDC 相比,西妥昔单抗为 NSCLC 患者带来了获益。与单独使用 PBDC 相比,小分子 TKI 联合 PBDC 具有略微的附加疗效。