© 2003 by BMJ Publishing Group Ltd & British Society of Gastroenterology
COMMENTARY
Aspirin
Aspirin: still learning about the wonder drug
Gastrointestinal and Other Cancers Research Group, National Cancer Institute, Division of Cancer Prevention, Bethesda, Maryland, USA
Correspondence to:
Correspondence to:
Dr E T Hawk
Gastrointestinal and Other Cancers Research Group, National Cancer Institute, Division of Cancer Prevention, EPN, Suite 2141, 6130 Executive Boulevard, Bethesda, MD 20892-7317, USA; eh51p@nih.gov
Aspirin, taken daily over at least one year, may exert chemopreventive effects against the early stages of colorectal carcinogenesis
Keywords: aberrant crypt foci; aspirin; chemoprevention; colon cancer; non-steroidal anti-inflammatory drugs
| The first 150 words of the full text of this article appear below. |
Preclinical, observational, and clinical data consistently show that non-steroidal anti-inflammatory drugs (NSAIDs)particularly aspirinreduce colorectal carcinogenesis.1 Scores of animal studies show that NSAIDs inhibit the development of colorectal neoplasia across the spectrum of disease, ranging from aberrant crypt foci (ACF) to cancer.2 Human data confirm these findings with dozens of observational studies reporting 4050% reductions in colorectal adenoma incidence, cancer incidence, and cancer associated mortality among aspirin users. The most compelling data were published earlier this year. Two randomised placebo controlled trials conducted in patients at moderate risk for colorectal cancer reported that aspirin administered at doses as low as 81325 mg/day reduced the development of adenomas by up to 35% after a few years of use.3,4 In one trial, greater effects were seen against more advanced lesions.3
Colorectal adenomas are established as common non-obligate precursors of colorectal cancer.5 Within the last decade, ACF have been identified in rodent models
Relevant Article
- Suppressive effect of aspirin on aberrant crypt foci in patients with colorectal cancer
- B Shpitz, E Klein, G Buklan, D Neufeld, A Nissan, H R Freund, M Grankin, and J Bernheim
Gut 2003 52: 1598-1601.[Abstract] [Full Text] [PDF]
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