Epidemiology

British Journal of Cancer (2003) 88, 1687–1692. doi:10.1038/sj.bjc.6600945 www.bjcancer.com
Published online 27 May 2003

Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study

H T Sørensen1,2, S Friis3, B Nørgård1, L Mellemkjær3, W J Blot2,4, J K McLaughlin2,4, A Ekbom5 and J A Baron6

  1. 1Department of Clinical Epidemiology, Aarhus University and Aalborg Hospital, Vennelyst Boulevard 6, Building 260, DK-8000 Aarhus C, Denmark
  2. 2Department of Medicine, Vanderbilt University Medical Center and the Vanderbilt-Ingram Cancer Center, Nashville, TN, USA
  3. 3Institute of Cancer Epidemiology, The Danish Cancer Society, Strandboulevarden 49, DK-2100 Copenhagen Ø, Denmark
  4. 4International Epidemiology Institute, Ltd, 1455 Research Blvd., Suite 550, Rockville, MD 20850, USA
  5. 5Unit of Clinical Epidemiology, Department of Medicine, Karolinska Hospital, Box 281, SE-171 77 Stockholm, Sweden
  6. 6Departments of Medicine and Community and Family Medicine, Dartmouth Medical School, Hanover, NH 03756, USA

Correspondence: Dr HT Sørensen, Department of Clinical Epidemiology, Vennelyst Boulevard 6, Building 260, DK-8000 Aarhus C, Denmark. E-mail: hts@soci.au.dk

Received 5 December 2002; Revised 26 February 2003; Accepted 28 February 2003.

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Abstract

There is increasing evidence of an inverse association between use of nonsteroidal anti-inflammatory drugs (NSAIDs) and risk of colorectal cancer. However, data regarding other cancer sites are limited. Using data from the population-based North Jutland Prescription Database and the Danish Cancer Registry, we compared cancer incidence among 172 057 individuals prescribed nonaspirin NSAIDs with expected incidence (based on county-specific cancer rates) during a 9-year study period. A total of 6081 incident cancer cases were diagnosed among NSAID users vs 5722 expected (standardised incidence ratio (SIR) 1.1, 95% confidence interval (CI)1.0–1.1). The SIRs for colon and rectal cancer among persons who obtained 10 or more prescriptions were 0.7 (95% CI 0.6–0.9) and 0.6 (95% CI 0.4–0.9), respectively. Similarly, reduced risk estimates were found for stomach (SIR 0.7, 95% CI 0.4–1.1) and ovarian cancer (SIR 0.7, 95% CI 0.4–1.0). Standardised incidence ratios for other cancers among those with 10 or more prescriptions tended to be close to 1.0, except for lung, kidney, and prostate cancers with SIRs of 1.3 (95% CI 1.1–1.6), 1.4 (95% CI 0.9–2.1), and 1.6 (95% CI 1.3–2.0), respectively. We found protective associations of NSAIDs against colon, rectal, stomach, and ovarian cancer. Reasons for the increased risk for some cancer sites are not clear.

Keywords:

NSAIDs, epidemiology, risk, prevention

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