Low-Dose Aspirin in the Primary Prevention of Cancer: The Women’s Health Study: A Randomized Controlled Trial
CONTEXT Basic research and observational evidence as well as results from trials of colon polyp recurrence suggest a role for aspirin in the chemoprevention of cancer. OBJECTIVE To examine the effect of aspirin on the risk of cancer among healthy women. DESIGN, SETTING, AND PARTICIPANTS In the Women...
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Veröffentlicht in: | JAMA : the journal of the American Medical Association 2005-07, Vol.294 (1), p.47-55 |
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Zusammenfassung: | CONTEXT Basic research and observational evidence as well as results from trials
of colon polyp recurrence suggest a role for aspirin in the chemoprevention
of cancer. OBJECTIVE To examine the effect of aspirin on the risk of cancer among healthy
women. DESIGN, SETTING, AND PARTICIPANTS In the Women’s Health Study, a randomized 2 × 2
factorial trial of aspirin and vitamin E conducted between September 1992
and March 2004, 39 876 US women aged at least 45 years and initially
without previous history of cancer, cardiovascular disease, or other major
chronic illness were randomly assigned to receive either aspirin or aspirin
placebo and followed up for an average of 10.1 years. INTERVENTION A dose of 100 mg of aspirin (n=19 934) or aspirin placebo (n=19 942)
administered every other day. MAIN OUTCOME MEASURES Confirmed newly diagnosed invasive cancer at any site, except for nonmelanoma
skin cancer. Incidence of breast, colorectal, and lung cancer were secondary
end points. RESULTS No effect of aspirin was observed on total cancer (n = 2865;
relative risk [RR], 1.01; 95% confidence interval [CI], 0.94-1.08; P = .87), breast cancer (n = 1230; RR, 0.98; 95%
CI, 0.87-1.09; P = .68), colorectal cancer
(n = 269; RR, 0.97; 95% CI, 0.77-1.24; P = .83),
or cancer of any other site, with the exception of lung cancer for which there
was a trend toward reduction in risk (n = 205; RR, 0.78; 95% CI,
0.59-1.03; P = .08). There was also no
reduction in cancer mortality either overall (n = 583; RR, 0.95;
95% CI, 0.81-1.11; P = .51) or by site,
except for lung cancer mortality (n = 140; RR, 0.70; 95% CI, 0.50-0.99; P = .04). No evidence of differential effects
of aspirin by follow-up time or interaction with vitamin E was found. CONCLUSIONS Results from this large-scale, long-term trial suggest that alternate
day use of low-dose aspirin (100 mg) for an average 10 years of treatment
does not lower risk of total, breast, colorectal, or other site-specific cancers.
A protective effect on lung cancer or a benefit of higher doses of aspirin
cannot be ruled out. |
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ISSN: | 0098-7484 1538-3598 |
DOI: | 10.1001/jama.294.1.47 |