Author Affiliations Abstract Aspirin and other
nonsteroidal antiinflammatory drugs inhibit prostagiandin synthesis and tumor growth in many experimental systems, but it
is unclear which of these tumor models are relevant to humans. We have reported reduced risk of fatal colon cancer among persons
who used aspirin in a large prospective study. This analysis examines other fatal cancers in relation to aspirin among 635,031
adults in that study who provided information in 1982 on the frequency and duration of their aspirin use and did not report
cancer. Death rates were measured through 1988. Death rates decreased with more frequent aspirin use for cancers of the esophagus,
stomach, colon, and rectum but not generally for other cancers. For each digestive tract cancer, death
rates were approximately 40% lower among persons who used aspirin 16 times/month or more for at least 1 year compared to those
who used no aspirin. The trend of decreasing risk with more frequent aspirin use was strongest among persons who had
used aspirin for 10 years or more; it remained statistically significant, except for esophageal cancer, in multivariate analyses
that adjusted for other known risk factors. Biases such as early detection or aspirin avoidance among cases do not appear
to explain the results. Our data suggest that regular, prolonged use of aspirin may reduce the risk of fatal cancer of the
esophagus, stomach, colon, and rectum. Future epidemiological and basic research should examine all digestive tract cancers
in considering the chemopreventive or therapeutic potential of nonsteroidal antiinflammatory drugs. Footnotes
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