A meta-analysis of adjuvant EGFR-TKIs for patients with resected non-small cell lung cancer

被引:38
作者
Cheng, Hua [1 ]
Li, Xiao-Jian [1 ]
Wang, Xiao-Jin [1 ]
Chen, Zuo-Wen [1 ]
Wang, Rui-Qi [1 ]
Zhong, Hong-Cheng [1 ]
Wu, Tian-Chi [1 ]
Cao, Qing-Dong [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Thorac Surg, Guangzhou, Guangdong, Peoples R China
关键词
Non-small cell lung cancer (NSCLC); Epidermal growth factor receptor-tyrosine; kinase inhibitor (EGFR-TKI); Adjuvant therapy; Targeted therapy; Surgery; Gefitinib; Erlotinib; Osimertinib; Icotinib; Dacomitinib; Meta-analysis; POSTOPERATIVE RADIOTHERAPY; GEFITINIB; CHEMOTHERAPY; PLACEBO; MUTATIONS; AZD9291; PLUS; IIIA; CARE;
D O I
10.1016/j.lungcan.2019.08.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: We performed this meta-analysis to compare adjuvant EGFR-TKIs with a placebo or adjuvant chemotherapy among patients with resected non-small cell lung cancer (NSCLC). Materials and Methods: A literature search was performed using relevant keywords. All randomized controlled trials (RCTs) that compared the survival benefits of adjuvant EGFR-TKIs with those of placebo or adjuvant chemotherapy for resected NSCLC were eligible for inclusion. Results: The literature search yielded five eligible RCTs including three RCTs that compared adjuvant EGFR-TKIs with a placebo, and two RCTs that compared adjuvant EGFR-TKIs with chemotherapy. For unselected intent-to-treat patients who received adjuvant EGFR-TKIs versus a placebo, the hazard ratio (HR) of disease-free survival (DFS) was 0.88 (95% confidence interval (CI): 0.59-1.32; P = 0.54). For patients with an EGFR mutation, the DFS after adjuvant EGFR-TKIs was superior to that after a placebo, with a HR of 0.59 (95% CI: 0.40-0.88; P = 0.009). For patients with an EGFR mutation, the DFS after EGFR-TKIs was greater than that after chemotherapy, with a HR of 0.42 (95% CI: 0.19-0.93; P = 0.03). For patients with wild-type EGFR, the DFS of adjuvant EGFR-TKIs was similar to the placebo, with a RR of 1.00 (95% CI: 0.62-1.60; P = 0.99). Treatment with EGFR-TKIs resulted in more adverse events compared with the placebo, with a risk ratio (RR) of 2.72, (95% CI: 2.23-3.33; P < 0.00001), but fewer adverse events compared with chemotherapy, with an RR of 0.26 (95% CI: 0.18-0.38; P < 0.00001). Conclusions: For patients with resected NSCLC harboring EGFR mutations, treatment with an adjuvant EGFR-TKI was superior to that of a placebo or chemotherapy in terms of DFS. Treatment with adjuvant EGFR-TKIs were not effective among patients with wild type EGFR NSCLC.
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收藏
页码:7 / 13
页数:7
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