Analysis of lung cancer incidence in the nurses’ health and the health professionals’ follow-up studies using a multistage carcinogenesis model

We analyzed lung cancer incidence among non-smokers, continuing smokers, and ex-smokers in the Nurses Health Study (NHS) and the Health Professionals Follow-Up Study (HPFS) using the two-stage clonal expansion (TSCE) model. Age-specific lung cancer incidence rates among non-smokers are identical in the two cohorts. Within the framework of the model, the main effect of cigarette smoke is on the promotion of partially altered cells on the pathway to cancer. Smoking-related promotion is somewhat higher among women, whereas smoking-related malignant conversion is somewhat lower. In both cohorts the relative risk for a given daily level of smoking is strongly modified by duration. Among smokers, the incidence in NHS relative to that in HPFS depends both on smoking intensity and duration. The age-adjusted risk is somewhat larger in NHS, but not significantly so. After smokers quit, the risk decreases over a period of many years and the temporal pattern of the decline is similar to that reported in other recent studies. Among ex-smokers, the incidence in NHS relative to that in HPFS depends both on previous levels of smoking and on time since quitting. The age-adjusted risk among ex-smokers is somewhat higher in NHS, possibly due to differences in the age-distribution between the two cohorts.

[1]  Chris Bain,et al.  Lung cancer rates in men and women with comparable histories of smoking. , 2004, Journal of the National Cancer Institute.

[2]  B Rachet,et al.  A flexible modeling approach to estimating the component effects of smoking behavior on lung cancer. , 2004, Journal of clinical epidemiology.

[3]  W F Heidenreich,et al.  Some Properties of the Hazard Function of the Two‐Mutation Clonal Expansion Model , 1997, Risk analysis : an official publication of the Society for Risk Analysis.

[4]  W F Heidenreich,et al.  Analysis of a Historical Cohort of Chinese Tin Miners with Arsenic, Radon, Cigarette Smoke, and Pipe Smoke Exposures Using the Biologically Based Two-Stage Clonal Expansion Model , 2001, Radiation research.

[5]  T. Perneger Sex, smoking, and cancer: a reappraisal. , 2001, Journal of the National Cancer Institute.

[6]  J. Wellmann,et al.  Mechanistic modelling in large case‐control studies of lung cancer risk from smoking , 2002, Statistics in medicine.

[7]  J. Mclaughlin,et al.  Are women more susceptible to lung cancer? , 2004, Journal of the National Cancer Institute.

[8]  J. Siegfried,et al.  Expression of mRNA for gastrin-releasing peptide receptor by human bronchial epithelial cells. Association with prolonged tobacco exposure and responsiveness to bombesin-like peptides. , 1997, American journal of respiratory and critical care medicine.

[9]  S. Moolgavkar,et al.  Two-event models for carcinogenesis: incidence curves for childhood and adult tumors☆ , 1979 .

[10]  J H Lubin,et al.  The use of sliding time windows for the exploratory analysis of temporal effects of smoking histories on lung cancer risk. , 2000, Statistics in medicine.

[11]  J. Luketich,et al.  Sex-specific expression of gastrin-releasing peptide receptor: relationship to smoking history and risk of lung cancer. , 2000, Journal of the National Cancer Institute.

[12]  Peter B Bach,et al.  Lung cancer in US women: a contemporary epidemic. , 2004, JAMA.

[13]  Richard Doll,et al.  Smoking, smoking cessation, and lung cancer in the UK since 1950: combination of national statistics with two case-control studies , 2000, BMJ : British Medical Journal.

[14]  Michal Abrahamowicz,et al.  Modeling smoking history: a comparison of different approaches. , 2002, American journal of epidemiology.

[15]  E. Wynder,et al.  Differences in lung cancer risk between men and women: examination of the evidence. , 1996, Journal of the National Cancer Institute.

[16]  L. Holmberg,et al.  Lung cancer incidence in never smokers. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[17]  A. Miller,et al.  Are female smokers at higher risk for lung cancer than male smokers? A case-control analysis by histologic type. , 1993, American journal of epidemiology.

[18]  Peter Green,et al.  Markov chain Monte Carlo in Practice , 1996 .

[19]  E. Luebeck,et al.  Biologically based analysis of the data for the Colorado uranium miners cohort: age, dose and dose-rate effects. , 1999, Radiation research.

[20]  C. Begg,et al.  Variations in lung cancer risk among smokers. , 2003, Journal of the National Cancer Institute.

[21]  P. Vineis,et al.  Analysis of epidemiological cohort data on smoking effects and lung cancer with a multi-stage cancer model. , 2006, Carcinogenesis.

[22]  Mark S. Clements,et al.  Multistage Carcinogenesis and Lung Cancer Mortality in Three Cohorts , 2005, Cancer Epidemiology Biomarkers & Prevention.

[23]  S H Moolgavkar,et al.  Mutation and cancer: a model for human carcinogenesis. , 1981, Journal of the National Cancer Institute.