Non-steroidal anti-inflammatory drugs and cancer risk in women: Results from the Women's Health Initiative

被引:63
作者
Brasky, Theodore M. [1 ,2 ]
Liu, Jingmin [3 ]
White, Emily [2 ,4 ]
Peters, Ulrike [2 ]
Potter, John D. [2 ,5 ]
Walter, Roland B. [2 ,4 ,6 ]
Baik, Christina S. [2 ]
Lane, Dorothy S. [7 ]
Manson, JoAnn E. [8 ,9 ]
Vitolins, Mara Z. [10 ]
Allison, Matthew A. [11 ]
Tang, Jean Y. [12 ]
Wactawski-Wende, Jean [13 ]
机构
[1] Ohio State Univ, Dept Internal Med, Div Canc Prevent & Control, Coll Med, Columbus, OH 43201 USA
[2] Fred Hutchinson Canc Res Ctr, Canc Prevent Program, Seattle, WA 98104 USA
[3] Fred Hutchinson Canc Res Ctr, WHI Clin Coordinating Ctr, Seattle, WA 98104 USA
[4] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[5] Massey Univ, Ctr Publ Hlth Res, Wellington, New Zealand
[6] Univ Washington, Dept Med, Div Hematol, Seattle, WA 98195 USA
[7] SUNY Stony Brook, Dept Prevent Med, Stony Brook, NY 11794 USA
[8] Harvard Univ, Sch Med, Boston, MA USA
[9] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[10] Wake Forest Sch Med, Div Publ Hlth Sci, Winston Salem, NC USA
[11] Univ Calif San Diego, Sch Med, Div Prevent Med, Dept Family & Prevent Med, San Diego, CA 92103 USA
[12] Stanford Univ, Dept Dermatol, Sch Med, Redwood City, CA USA
[13] SUNY Buffalo, Dept Social & Prevent Med, Buffalo, NY 14260 USA
基金
美国国家卫生研究院;
关键词
aspirin; cancer; ibuprofen; inflammation; naproxen; non-steroidal anti-inflammatory drug; BASE-LINE CHARACTERISTICS; LOW-DOSE ASPIRIN; RANDOMIZED CONTROLLED-TRIALS; C-REACTIVE PROTEIN; BREAST-CANCER; COLORECTAL-CANCER; ENDOMETRIAL CANCER; MELANOMA RISK; LARGE COHORT; LUNG-CANCER;
D O I
10.1002/ijc.28823
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The use of non-steroidal anti-inflammatory drugs (NSAIDs) has been associated with reduced risks of cancers at several sites in some studies; however, we recently reported no association between their use and total cancer risk in women in a prospective study. Here we examine the association between NSAIDs and total and site-specific cancer incidence in the large, prospective Women's Health Initiative (WHI). Women (129,013) were recruited to participate in the WHI at 40 US clinical centers from 1993 to 1998 and followed prospectively. After 9.7 years of follow-up, 12,998 incident, first primary, invasive cancers were diagnosed. NSAID use was systematically collected at study visits. We used Cox proportional hazards regression models to estimate multivariable-adjusted hazard ratios (HR) and 95% confidence intervals (CI) for associations between NSAIDs use and total and site-specific cancer risk. Relative to non-use, consistent use (i.e., use at baseline and year 3 of follow-up) of any NSAID was not associated with total cancer risk (HR 1.00, 95% CI: 0.94-1.06). Results for individual NSAIDs were similar to the aggregate measure. In site-specific analyses, NSAIDs were associated with reduced risks of colorectal cancer, ovarian cancer, and melanoma. Our study confirms a chemopreventive benefit for colorectal cancer in women and gives preliminary evidence for a reduction of the risk of some rarer cancers. NSAIDs' benefit on cancer risk was therefore limited to specific sites and not evident when total cancer risk was examined. This information may be of importance when NSAIDs are considered as chemopreventive agents.
引用
收藏
页码:1869 / 1883
页数:15
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