Cancer diagnosis in first-degree relatives and non-small cell lung cancer risk: Results from a multi-centre case-control study in Europe

被引:15
作者
Cassidy, Adrian [1 ,2 ]
Balsan, Jessica [3 ]
Vesin, Aurelien [3 ]
Wu, Xifeng [2 ]
Liloglou, Triantafillos [1 ]
Brambilla, Christian [4 ]
Timsit, Jean-Francois [3 ]
Field, John K. [1 ]
机构
[1] Univ Liverpool, Roy Castle Lung Canc Res Programme, Canc Res Ctr, Liverpool L69 3BX, Merseyside, England
[2] Univ Texas MD Anderson Canc Ctr, Dept Epidemiol, Houston, TX 77030 USA
[3] INSERM, U823, Inst Albert Bonniot, Team Outcome Canc & Crit Illnesses 11, Grenoble, France
[4] Univ Grenoble 1, INSERM, U823, Inst Albert Bonniot, Grenoble, France
关键词
Family history; Non-small cell lung cancer; Genetic susceptibility; FAMILY-HISTORY; SUSCEPTIBILITY LOCUS; AGGREGATION; ASSOCIATION;
D O I
10.1016/j.ejca.2009.05.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Because aggregation of cancers at different sites can occur in families, cancer could be considered as a broad phenotype with shared genetic factors. Here, we report results from a multi-centre case-control study of non-small cell lung cancer (NSCLC), with particular emphasis on a history of cancer in first-degree relatives and the risk of lung cancer. From 2002 to 2006, 733 NSCLC patients treated surgically were recruited in 8 European countries and matched to 1312 controls, by Centre, sex and age. We used multivariate conditional logistic regression models to test the association between a history of cancer in first-degree relatives and risk of NSCLC. A family history of lung cancer was associated with an odds ratio (OR) for early-onset (54 years or younger) NSCLC of 4.72 (95% confidence interval [CI] = 1.02-21.90). A family history of gastric cancer was associated with an OR for NSCLC of 1.82 (95% CI = 1.08-3.06) and for late-onset (55 years or older) NSCLC of 2.92 (95% CI = 1.10-7.75). Our findings provide further evidence of a familial predisposition to lung cancer and support the hypothesis that family history is a significant risk factor for the disease. Because of the inherent potential for bias in familial case-control study design, cautious interpretation is warranted. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3047 / 3053
页数:7
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