Increased risk of lung cancer in individuals with a family history of the disease: A pooled analysis from the International Lung Cancer Consortium

被引:121
作者
Cote, Michele L. [1 ,2 ]
Liu, Mei [3 ]
Bonassi, Stefano [4 ]
Neri, Monica [4 ]
Schwartz, Ann G. [1 ,2 ]
Christiani, David C. [5 ]
Spitz, Margaret R. [3 ]
Muscat, Joshua E. [6 ]
Rennert, Gad [7 ,8 ,9 ]
Aben, Katja K. [10 ]
Andrew, Angeline S. [11 ]
Bencko, Vladimir [12 ,15 ]
Bickeboeller, Heike [13 ]
Boffetta, Paolo [14 ]
Brennan, Paul
Brenner, Hermann [16 ]
Duell, Eric J. [17 ]
Fabianova, Eleonora [18 ]
Field, John K. [19 ]
Foretova, Lenka
Friis, Soren
Harris, Curtis C. [20 ]
Holcatova, Ivana [12 ,15 ]
Hong, Yun-Chul [21 ]
Isla, Dolores [22 ]
Janout, Vladimir [23 ]
Kiemeney, Lambertus A. [24 ,25 ,31 ,32 ]
Kiyohara, Chikako [26 ]
Lan, Qing [27 ]
Lazarus, Philip [28 ]
Lissowska, Jolanta [29 ,30 ]
Le Marchand, Loic [33 ]
Mates, Dana [34 ]
Matsuo, Keitaro [35 ]
Mayordomo, Jose I.
McLaughlin, John R. [36 ]
Morgenstern, Hal [37 ]
Mueeller, Heiko [16 ]
Orlow, Irene [38 ]
Park, Bernard J. [39 ]
Pinchev, Mila [7 ,8 ,9 ]
Raji, Olaide Y. [19 ]
Rennert, Hedy S. [7 ,8 ,9 ]
Rudnai, Peter [40 ]
Seow, Adeline [41 ]
Stucker, Isabelle [42 ]
Szeszenia-Dabrowska, Neonila [43 ]
Teare, M. Dawn [44 ]
Tjonnelan, Anne
Ugolini, Donatella [45 ]
机构
[1] Wayne State Univ, Sch Med, Detroit, MI 48202 USA
[2] Wayne State Univ, Karmanos Canc Inst, Detroit, MI 48202 USA
[3] MD Anderson Canc Ctr, Dept Epidemiol, Houston, TX USA
[4] Clin & Mol Epidemiol IRCCS San Raffaele Pisana, Pisa, Italy
[5] Harvard Univ, Sch Publ Hlth, Cambridge, MA 02138 USA
[6] Penn State Univ, Coll Med, Div Publ Hlth Sci, University Pk, PA 16802 USA
[7] Technion Israel Inst Technol, Bruce Rappaport Fac Med, Haifa, Israel
[8] Technion Israel Inst Technol, Dept Community Med & Epidemiol, Carmel Med Ctr, Haifa, Israel
[9] Technion Israel Inst Technol, CHS Natl Canc Control Ctr, Haifa, Israel
[10] Comprehens Canc Ctr Netherlands, Nijmegen, Netherlands
[11] Dartmouth Med Sch, Dept Community & Family Med, Norris Cotton Canc Ctr, Lebanon, NH USA
[12] Charles Univ Prague, Inst Hyg & Epidemiol, Prague, Czech Republic
[13] Univ Gottingen, Sch Med, Dept Genet Epidemiol, D-3400 Gottingen, Germany
[14] Mt Sinai Sch Med, New York, NY USA
[15] IARC, Lyon, France
[16] German Canc Res Ctr, Div Clin Epidemiol & Aging Res, Heidelberg, Germany
[17] Catalan Inst Oncol ICO IDIBELL, Unit Nutr Environm & Canc, Barcelona, Spain
[18] Specialized State Hlth Inst, Dept Occupat Hlth, Banska Bystrica, Slovakia
[19] Univ Liverpool, Canc Res Ctr, Roy Castle Lung Canc Res Programme, Liverpool L69 3BX, Merseyside, England
[20] Natl Canc Inst, Mol Genet & Carcinogenesis Sect, Bethesda, MD 20892 USA
[21] Seoul Natl Univ, Seoul 151, South Korea
[22] Univ Zaragoza, Div Med Oncol, E-50009 Zaragoza, Spain
[23] Palacky Univ Med, Dept Prevent Med, Olomouc, Czech Republic
[24] Radboud Univ Nijmegen, Med Ctr, Dept Urol, Nijmegen, Netherlands
[25] Radboud Univ Nijmegen, Nijmegen Med Ctr, Dept Urol, Nijmegen, Netherlands
[26] Kyushu Univ, Dept Basic Med, Fukuoka 812, Japan
[27] Natl Canc Inst, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[28] Penn State Univ, Penn State Canc Inst, University Pk, PA 16802 USA
[29] Maria Sklodowska Curie Inst Oncol, Warsaw, Poland
[30] Ctr Canc, Dept Canc Epidemiol & Prevent, Warsaw, Poland
[31] Radboud Univ Nijmegen, Dept Epidemiol, Nijmegen, Netherlands
[32] Radboud Univ Nijmegen, HTA, Nijmegen, Netherlands
[33] Univ Hawaii, Ctr Canc, Honolulu, HI 96822 USA
[34] Inst Publ Hlth, Dept Occupat Hlth, Bucharest, Romania
[35] Res Inst, Aichi Canc Ctr, Aichi, Japan
[36] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON, Canada
[37] Univ Michigan, Sch Publ Hlth, Ann Arbor, MI 48109 USA
[38] Mem Sloan Kettering Canc, New York, NY USA
[39] Hackensack Univ, Med Ctr, Hackensack, NJ USA
[40] Fodor Jozsef Natl Ctr Publ Hlth, Natl Inst Environm Hlth, Budapest, Hungary
[41] Natl Univ Singapore, Yong Loo Lin Sch Med, Singapore 117595, Singapore
[42] INSERM, U170, Dept Environm Epidemiol, Paris, France
[43] Nofer Inst Occupat Med, Lodz, Poland
[44] Univ Sheffield, Sheffield, S Yorkshire, England
[45] Univ Genoa, Dipartimento Oncol Biol & Genet, I-16126 Genoa, Italy
[46] German Res Ctr Environm Hlth, Inst Epidemiol, Helmholtz Ctr, Munich, Germany
[47] Univ Calif San Francisco, Dept Epidemiol & Biostatist, San Francisco, CA 94143 USA
[48] Mayo Clin, Div Epidemiol, Rochester, MN USA
[49] NN Blokhin Canc Res Ctr, Inst Carcinogenesis, Moscow, Russia
[50] Univ Calif Los Angeles, Sch Publ Hlth, Dept Epidemiol, Los Angeles, CA 90024 USA
关键词
Lung cancer; Familial aggregation; POPULATION-BASED COHORT; SUSCEPTIBILITY LOCUS; SEQUENCE VARIANTS; PROSTATE-CANCER; NEVER-SMOKERS; SMOKING; ASSOCIATION; POLYMORPHISM; AGGREGATION; RELATIVES;
D O I
10.1016/j.ejca.2012.01.038
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and methods: Familial aggregation of lung cancer exists after accounting for cigarette smoking. However, the extent to which family history affects risk by smoking status, histology, relative type and ethnicity is not well described. This pooled analysis included 24 case-control studies in the International Lung Cancer Consortium. Each study collected age of onset/interview, gender, race/ethnicity, cigarette smoking, histology and first-degree family history of lung cancer. Data from 24,380 lung cancer cases and 23,305 healthy controls were analysed. Unconditional logistic regression models and generalised estimating equations were used to estimate odds ratios and 95% confidence intervals. Results: Individuals with a first-degree relative with lung cancer had a 1.51-fold increase in the risk of lung cancer, after adjustment for smoking and other potential confounders (95% CI: 1.39, 1.63). The association was strongest for those with a family history in a sibling, after adjustment (odds ratios (OR) = 1.82, 95% CI: 1.62, 2.05). No modifying effect by histologic type was found. Never smokers showed a lower association with positive familial history of lung cancer (OR = 1.25, 95% CI: 1.03, 1.52), slightly stronger for those with an affected sibling (OR = 1.44, 95% CI: 1.07, 1.93), after adjustment. Conclusions: The occurrence of lung cancer among never smokers and similar magnitudes of the effect of family history on lung cancer risk across histological types suggests familial aggregation of lung cancer is independent of those risks associated with cigarette smoking. While the role of genetic variation in the aetiology of lung cancer remains to be fully characterised, family history assessment is immediately available and those with a positive history represent a higher risk group. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1957 / 1968
页数:12
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