Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, People's Republic of China.
Environ Mol Mutagen. 2012 Jan;53(1):78-82. doi: 10.1002/em.20680. Epub 2011 Aug 29.
Mounting evidence has suggested somatic mutations in the EGFR gene are associated with better responsiveness to EGFR tyrosine kinase inhibitors (TKIs) in patients with non-small-cell lung cancer (NSCLC). Some, but not all, studies have reported that the mutations were more frequently observed in patients without a smoking history. To comprehensively address this issue, we performed a meta-analysis to evaluate the association between cigarette-smoking history and mutation of the EGFR gene in NSCLC. Twenty-six studies, involving 3,688 patients with NSCLC were included in the analysis. The pooled analysis shows that the incidence of EGFR mutations in NSCLC differs according to cigarette-smoking history. The odds ratio (OR) for the EGFR mutation in non-smokers relative to smokers was 4.829 (95% confidence interval [CI]: 3.598-6.482; P < 0.001). These data may assist clinicians in assessing the likelihood of EGFR mutations in patients with NSCLC when mutational analysis is not feasible.
越来越多的证据表明,表皮生长因子受体(EGFR)基因的体细胞突变与非小细胞肺癌(NSCLC)患者对 EGFR 酪氨酸激酶抑制剂(TKI)的更好反应性有关。一些(但不是全部)研究报告称,这些突变在无吸烟史的患者中更为常见。为了全面解决这个问题,我们进行了荟萃分析,以评估吸烟史与 NSCLC 中 EGFR 基因突变之间的关系。共有 26 项研究,涉及 3688 例 NSCLC 患者,纳入了分析。汇总分析表明,根据吸烟史,NSCLC 中 EGFR 基因突变的发生率不同。与吸烟者相比,不吸烟者 EGFR 基因突变的优势比(OR)为 4.829(95%置信区间[CI]:3.598-6.482;P<0.001)。这些数据可能有助于临床医生在无法进行突变分析时评估 NSCLC 患者 EGFR 突变的可能性。