Use of cigarette-smoking history to estimate the likelihood of mutations in epidermal growth factor receptor gene exons 19 and 21 in lung adenocarcinomas

被引:185
作者
Pham, DK
Kris, MG
Riely, GJ
Sarkaria, IS
McDonough, T
Chuai, SK
Venkatraman, ES
Miller, VA
Ladanyi, M
Pao, W
Wilson, RK
Singh, B
Rusch, VW
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10021 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
[5] Cornell Univ, Weill Med Coll, New York, NY USA
[6] Washington Univ, Genome Sequencing Ctr, St Louis, MO USA
关键词
D O I
10.1200/JCO.2005.04.3224
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Lung adenocarcinomas with mutations in exons 19 and 21 of the epidermal growth factor receptor gene (EGFR) demonstrate sensitivity to gefitinib or erlotinib. Investigators have reported an association between EGFR mutations and the amount and duration of cigarette smoking, with the highest incidence of mutations seen in never smokers. Methods EGFR exon 19 and 21 mutation status was determined in 265 tumor samples using direct sequencing, polymerase chain reaction (PCR), or PCR-based restriction fragment length polymorphism analysis. A detailed smoking history was obtained. Patients were categorized as never osmokers (< 100 lifetime cigarettes), former smokers (quit >= 1 year ago), or current smokers (quit< 1 year ago). Results We detected EGFR mutations in 34 (51%) of 67 never smokers (95% Cl, 38% to 64%), 29 (19%) of 151 former smokers (95% Cl, 13% to 27%), and two (4%) of 47 current smokers (95% Cl, 1% to 16%). Significantly fewer EGFR mutations were found in people who smoked for more than 15 pack-years (P <.001) or stopped smoking less than 25 years ago (P <.02) compared with individuals who never smoked. The number of smoking pack-years and smoke-free years predicted the prevalence of EGFR mutations (areas under receiver operating characteristic curve = 0.78 and 0.77, respectively). Conclusion The likelihood of EGFR mutations in exons 19 and 21 decreases as the number of pack-years increases. Mutations were less common in people who smoked for more than 15 pack-years or who stopped smoking cigarettes less than 25 years ago. These data can assist clinicians in assessing the likelihood of exon 19 and 21 EGFR mutations in patients with lung adenocarcinoma when mutational analysis is not feasible.
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页码:1700 / 1704
页数:5
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