Low-dose aspirin in the primary prevention of cancer the women's health study: A randomized controlled trial

被引:633
作者
Cook, NR
Lee, IM
Gaziano, JM
Gordon, D
Ridker, PM
Manson, JE
Hennekens, CH
Buring, JE
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med,Div Prevent Med, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med,Div Cardiovasc Med, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med,Div Aging, Boston, MA 02215 USA
[4] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dept Ambulatory Care & Prevent, Vet Affairs Boston Healthcare Syst, Boston, MA USA
[6] Univ Miami, Sch Med, Dept Med, Miami, FL USA
[7] Univ Miami, Sch Med, Dept Epidemiol & Publ Hlth, Miami, FL USA
[8] Florida Atlantic Univ, Ctr Excellence, Dept Biomed Sci, Boca Raton, FL 33431 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2005年 / 294卷 / 01期
关键词
D O I
10.1001/jama.294.1.47
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 X 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=19942) 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% Cl, 0.87-1.09; P=.68), colorectal cancer (n=269; RR, 0.97; 95% Cl, 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% Cl,-0.59-1.03; P=.08). There was also no reduction in cancer mortality either overall (n=583; RR, 0.95; 95% Cl, 0.81-1.11; P=.51) or by site, except for lung cancer mortality (n=140; RR, 0.70; 95% Cl, 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.
引用
收藏
页码:47 / 55
页数:9
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