Ii. Peleg et al., ASPIRIN AND NONSTEROIDAL ANTIINFLAMMATORY DRUG-USE AND THE RISK OF SUBSEQUENT COLORECTAL-CANCER, Archives of internal medicine, 154(4), 1994, pp. 394-399
Objective: To test the hypothesis that the regular use of aspirin and
other nonsteroidal anti-inflammatory drugs (NSAIDs) is negatively asso
ciated with the risk of subsequent colorectal cancer. Design: Case-con
trol study with four age- and sex-matched control subjects for each in
cident colorectal cancer case. Population and Setting: Patient populat
ion of a large municipal teaching hospital in Atlanta, Ga. Main Outcom
e Measure: Odds of colorectal cancer as a function of aspirin, nonaspi
rin NSAIDs, and acetaminophen dispensed to the study population in the
4 years prior to incident colorectal cancer diagnosis. Main Results:
The risk of colorectal cancer estimated by odds ratios decreased with
inceasing days of exposure to aspirin linearly in a dose-dependent fas
hion (likelihood ratio statistic: for cumulative days, P<.001; for cum
ulative dose, P<.001). The coefficient for days of exposure to aspirin
was highly significant even when modeled as a continuous variable (P=
.001). There appeared to be a threshold above which nonaspirin NSAIDs
afforded protection (likelihood ratio statistic: for cumulative days,
P=.021; for cumulative dose,P=.019). Acetaminophen conferred no risk r
eduction. Conclusion: The results of previous experimental animal mode
ls, interventional case studies, and some but not all epidemiological
investigations and the present data point toward a causal relationship
between NSAID use and the prevention of cancer of the large bowel and
rectum. Because of the potential gastrointestinal and renal side effe
cts of NSAID use, particularly in the elderly, chemoprevention trials
are now needed to allow risk-benefit analysis in populations at high r
isk for colorectal cancer.