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Aspirin for the chemoprevention of colorectal adenomas: meta-analysis of the randomized trials.

Publication ,  Journal Article
Cole, BF; Logan, RF; Halabi, S; Benamouzig, R; Sandler, RS; Grainge, MJ; Chaussade, S; Baron, JA
Published in: J Natl Cancer Inst
February 18, 2009

BACKGROUND: Multiple lines of evidence indicate that aspirin has an antineoplastic effect in the large bowel. Randomized clinical trials have been conducted to evaluate the effectiveness of aspirin for reducing the risk of colorectal adenomas. A meta-analysis of these trials will provide more precise estimates of the aspirin effect, both overall and in subgroups. METHODS: We combined data from all randomized double-blind placebo-controlled trials that evaluated aspirin for the prevention of colorectal adenomas. We used random-effects meta-analysis to estimate risk ratios and 95% confidence intervals (CIs) for the effect of aspirin on the occurrence of adenomas and of advanced lesions (ie, tubulovillous adenomas, villous adenomas, adenomas >or=1 cm in diameter, adenomas with high-grade dysplasia, or invasive cancer). All statistical tests were two-sided. RESULTS: We identified four clinical trials with 2967 randomly assigned participants. Each trial evaluated aspirin for the secondary prevention of colorectal adenomas. Doses of aspirin tested ranged from 81 to 325 mg/d. The average age of participants at baseline was 58 years, and 60% were male. Median follow-up was 33 months. A total of 2698 participants underwent colonoscopic follow-up and were included in the analysis of adenoma occurrence and advanced-lesion occurrence after randomization. Among these participants, adenomas were found in 424 (37%) of the 1156 participants allocated to placebo and in 507 (33%) of the 1542 participants allocated to any dose of aspirin. Advanced lesions were found in 12% of participants in the placebo group and in 9% of participants allocated to any dose of aspirin. The pooled risk ratio of any adenoma for any dose of aspirin vs placebo was 0.83 (95% CI = 0.72 to 0.96). This corresponded to an absolute risk reduction of 6.7% (95% CI = 3.2% to 10.2%). For any advanced lesion, the pooled risk ratio was 0.72 (95% CI = 0.57 to 0.90). We found no statistically significant effect modification for any of the baseline factors studied. CONCLUSION: Aspirin is effective for the prevention of colorectal adenomas in individuals with a history of these lesions.

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Published In

J Natl Cancer Inst

DOI

EISSN

1460-2105

Publication Date

February 18, 2009

Volume

101

Issue

4

Start / End Page

256 / 266

Location

United States

Related Subject Headings

  • Research Design
  • Randomized Controlled Trials as Topic
  • Oncology & Carcinogenesis
  • Odds Ratio
  • Neoplasm Recurrence, Local
  • Middle Aged
  • Medication Adherence
  • Male
  • Humans
  • Female
 

Citation

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Cole, B. F., Logan, R. F., Halabi, S., Benamouzig, R., Sandler, R. S., Grainge, M. J., … Baron, J. A. (2009). Aspirin for the chemoprevention of colorectal adenomas: meta-analysis of the randomized trials. J Natl Cancer Inst, 101(4), 256–266. https://doi.org/10.1093/jnci/djn485
Cole, Bernard F., Richard F. Logan, Susan Halabi, Robert Benamouzig, Robert S. Sandler, Matthew J. Grainge, Stanislas Chaussade, and John A. Baron. “Aspirin for the chemoprevention of colorectal adenomas: meta-analysis of the randomized trials.J Natl Cancer Inst 101, no. 4 (February 18, 2009): 256–66. https://doi.org/10.1093/jnci/djn485.
Cole BF, Logan RF, Halabi S, Benamouzig R, Sandler RS, Grainge MJ, et al. Aspirin for the chemoprevention of colorectal adenomas: meta-analysis of the randomized trials. J Natl Cancer Inst. 2009 Feb 18;101(4):256–66.
Cole, Bernard F., et al. “Aspirin for the chemoprevention of colorectal adenomas: meta-analysis of the randomized trials.J Natl Cancer Inst, vol. 101, no. 4, Feb. 2009, pp. 256–66. Pubmed, doi:10.1093/jnci/djn485.
Cole BF, Logan RF, Halabi S, Benamouzig R, Sandler RS, Grainge MJ, Chaussade S, Baron JA. Aspirin for the chemoprevention of colorectal adenomas: meta-analysis of the randomized trials. J Natl Cancer Inst. 2009 Feb 18;101(4):256–266.
Journal cover image

Published In

J Natl Cancer Inst

DOI

EISSN

1460-2105

Publication Date

February 18, 2009

Volume

101

Issue

4

Start / End Page

256 / 266

Location

United States

Related Subject Headings

  • Research Design
  • Randomized Controlled Trials as Topic
  • Oncology & Carcinogenesis
  • Odds Ratio
  • Neoplasm Recurrence, Local
  • Middle Aged
  • Medication Adherence
  • Male
  • Humans
  • Female