Use of Nonsteroidal Anti-inflammatory Drugs and Risk of Ovarian and Endometrial Cancer: The Multiethnic Cohort

被引:39
作者
Setiawan, Veronica Wendy [1 ]
Matsuno, Rayna K. [2 ]
Lurie, Galina [2 ]
Wilkens, Lynne R. [2 ]
Carney, Michael E. [2 ]
Henderson, Brian E. [1 ]
Kolonel, Laurence N. [2 ]
Goodman, Marc T. [2 ]
机构
[1] Univ So Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA 90033 USA
[2] Univ Hawaii, Ctr Canc, Honolulu, HI 96822 USA
关键词
PELVIC-INFLAMMATORY-DISEASE; REACTIVE PROTEIN CONCENTRATIONS; CELL-GROWTH; MEDICATION USE; WOMENS HEALTH; ANALGESIC USE; ASPIRIN; ACETAMINOPHEN; ASSOCIATION; CARCINOMA;
D O I
10.1158/1055-9965.EPI-12-0390-T
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Chronic inflammation may play an etiologic role in ovarian and endometrial cancer, and it is hypothesized that nonsteroidal anti-inflammatory drugs (NSAID) decrease the risk of developing these malignancies. No prospective study with a large multiethnic population has explored this hypothesis. Methods: We investigated whether NSAID use was associated with risks of ovarian and endometrial cancer in the Multiethnic Cohort Study. Medication use of at least twice a week for >= 1 month was assessed at baseline. Multivariable relative risks (RR) and 95% confidence intervals (CI) were estimated using Cox proportional hazards models. Results: During 13.3 years of follow-up, 275 ovarian and 620 endometrial incident cases were identified among approximately 64,000 women included in this analysis (16.5% African Americans, 30.8% Japanese, 7.7% Native Hawaiians, 18.9%, Latinas, and 26.0% whites). The RR (95% CI) for ovarian cancer associated with aspirin, non-aspirin NSAIDs, and acetaminophen were 0.87 (0.68-1.14), 0.97 (0.74-1.26), and 0.86 (0.67-1.12), respectively. The RR (95% CI) for endometrial cancer associated with aspirin, non-aspirin NSAIDs, and acetaminophen were 0.93 (0.79-1.10), 0.88 (0.74-1.05), and 0.96 (0.81-1.13), respectively. No heterogeneity across ethnic groups (P >= 0.29) or dose-response relation with increased duration of use (P-trend >= 0.16) was observed. The results did not differ by tumor histology. Conclusions: We found no compelling evidence to support an association between the use of NSAIDs and risk of ovarian and endometrial cancers in a multiethnic population. Impact: It is unlikely that NSAID is involved in the etiology of endometrial and ovarian cancer. Cancer Epidemiol Biomarkers Prev; 21(9); 1441-9. (C) 2012 AACR.
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页码:1441 / 1449
页数:9
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