4.5 Article

A Pooled Analysis of Smoking and Colorectal Cancer: Timing of Exposure and Interactions with Environmental Factors

Journal

CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
Volume 21, Issue 11, Pages 1974-1985

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1055-9965.EPI-12-0692

Keywords

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Funding

  1. National Cancer Institute, NIH under RFA [CA-95-011]
  2. Australasian Colorectal Cancer Family Registry [U01 CA097735]
  3. Mayo Clinic Cooperative Family Registry for Colon Cancer Studies [U01 CA074800]
  4. Seattle Colorectal Cancer Family Registry [U01 CA074794]
  5. Ontario Registry for Studies of Familial Colorectal Cancer [U01 CA074783]
  6. Ontario Research Fund
  7. Canadian Institutes of Health Research
  8. Cancer Risk Evaluation (CaRE) Program grant from the Canadian Cancer Society Research Institute
  9. NIH [P01 CA 055075, R01 137178, P50 CA 127003]
  10. Intramural Research Program of the Division of Cancer Epidemiology and Genetics
  11. Division of Cancer Prevention, National Cancer Institute, U.S. Department of Health and Human Services
  12. Intramural Research Program of the National Cancer Institute
  13. NIH from the National Cancer Institute and Office of Dietary Supplements [K05 CA154337]
  14. National Heart, Lung, and Blood Institute, NIH, U.S. Department of Health and Human Services [HHSN268201100046C, HHSN268201100001C, HHSN268201100002C, HHSN268201100003C, HHSN268201100004C, HHSN271201100004C]

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Background: Considerable evidence suggests that cigarette smoking is associated with a higher risk of colorectal cancer (CRC). What is unclear, however, is the impact of quitting smoking on risk attenuation and whether other risk factors for CRC modify this association. Methods: We conducted a pooled analysis of eight studies, including 6,796 CRC cases and 7,770 controls, to evaluate the association between cigarette smoking history and CRC risk and to investigate potential effect modification by other risk factors. Results: Current smokers [OR, 1.26; 95% confidence interval (Cl), 1.11-1.43] and former smokers (OR, 1.18; 95% CI, 1.09-1.27), relative to never smokers, showed higher risks of CRC. Former smokers remained at higher CRC risk, relative to never smokers, for up to about 25 years after quitting. The impact of time since quitting varied by cancer subsite: The excess risk due to smoking decreased immediately after quitting for proximal colon and rectal cancer but not until about 20 years post-quitting for distal colon cancer. Furthermore, we observed borderline statistically significant additive interactions between smoking status and body mass index [BMI; relative excess risk due to interaction (RERI]), 0.15; 95% CI, -0.01 to 0.31; P = 0.06] and significant additive interaction between smoking status and fruit consumption (RERI, 0.16; 95% CI, 0.01-0.30; P = 0.04). Conclusion: CRC risk remained increased for about 25 years after quitting smoking, and the pattern of decline in risk varied by cancer subsite. BMI and fruit intake modified the risk associated with smoking. Impact: These results contribute to a better understanding of the mechanisms through which smoking impacts CRC etiology. Cancer Epidemiol Biomarkers Prev; 21(11); 1974-85. (C)2012 AACR.

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