Tomoya Kawaguchi 1 , Masahiko Ando , Akihito Kubo , Minoru Takada , Shinji Atagi , Kyoichi Okishio , Kazuhiro Asami , Akihide Matsumura , Kazuyuki Tsujino , Ou Sai-Hong Ignatius , Hidefumi Sasaki . Show Affiliations »
Abstract
PURPOSE: To examine an association between environmental tobacco smoke (ETS) and activating epidermal growth factor receptor (EGFR) mutations in never-smokers with non-small cell lung cancer (NSCLC). EXPERIMENTAL DESIGN: A total of 126 never-smokers with NSCLC were prospectively included in this study. Detailed ETS information was obtained through a standardized questionnaire including exposure period, place, and duration. Cumulative dose of ETS (CETS) was evaluated as a sum of the number of the exposure years at home and/or workplace. EGFR and K-ras mutations were determined using real-time PCR amplification. RESULTS: A total of 124 patients (98.4%) had ETS exposure with median CETS of 50 years (range: 0-118). Activating EGFR mutations were detected in 62.7% of the 126 patients and K-ras in 2 of 114 patients. The incidence of activating EGFR mutations was significantly higher in females than in males (67.6% vs. 26.7%; P = 0.002), and increased in quintile groups separated on the basis of CETS (shortest group = 44.0%, longest = 84.6%; P = 0.0033). In the multivariate logistic regression model, including gender, CETS, age, and family history of cancer, both gender and CETS were significantly associated with an incidence of activating EGFR mutations; the odds ratio for the EGFR mutations were 5.13 [95% confidence interval, CI = 1.47-18.0; P = 0.0105] for females and 1.02 (95% CI = 1.00-1.04; P = 0.0193) for each 1-year increment in CETS. CONCLUSIONS: Females and increased ETS exposure are closely associated with EGFR mutations in never-smokers with NSCLC. ©2010 AACR.
PURPOSE: To examine an association between environmental tobacco smoke (ETS) and activating epidermal growth factor receptor (EGFR ) mutations in never-smokers with non-small cell lung cancer (NSCLC ). EXPERIMENTAL DESIGN: A total of 126 never-smokers with NSCLC were prospectively included in this study. Detailed ETS information was obtained through a standardized questionnaire including exposure period, place, and duration. Cumulative dose of ETS (CETS ) was evaluated as a sum of the number of the exposure years at home and/or workplace. EGFR and K-ras mutations were determined using real-time PCR amplification. RESULTS: A total of 124 patients (98.4%) had ETS exposure with median CETS of 50 years (range: 0-118). Activating EGFR mutations were detected in 62.7% of the 126 patients and K-ras in 2 of 114 patients . The incidence of activating EGFR mutations was significantly higher in females than in males (67.6% vs. 26.7%; P = 0.002), and increased in quintile groups separated on the basis of CETS (shortest group = 44.0%, longest = 84.6%; P = 0.0033). In the multivariate logistic regression model, including gender, CETS , age, and family history of cancer , both gender and CETS were significantly associated with an incidence of activating EGFR mutations; the odds ratio for the EGFR mutations were 5.13 [95% confidence interval, CI = 1.47-18.0; P = 0.0105] for females and 1.02 (95% CI = 1.00-1.04; P = 0.0193) for each 1-year increment in CETS . CONCLUSIONS: Females and increased ETS exposure are closely associated with EGFR mutations in never-smokers with NSCLC . ©2010 AACR.
Entities: Chemical
Disease
Gene
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Year: 2010
PMID: 21059816 DOI: 10.1158/1078-0432.CCR-10-1773
Source DB: PubMed Journal: Clin Cancer Res ISSN: 1078-0432 Impact factor: 12.531