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Cancer Epidemiology Biomarkers & Prevention 16, 2262-2268, November 1, 2007. doi: 10.1158/1055-9965.EPI-07-0456
© 2007 American Association for Cancer Research

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Oral Contraceptive Use and Risk of Breast Carcinoma In situ

Hazel B. Nichols1, Amy Trentham-Dietz1,2, Kathleen M. Egan3, Linda Titus-Ernstoff4, John M. Hampton1 and Polly A. Newcomb5

1 University of Wisconsin Paul P. Carbone Comprehensive Cancer Center and 2 Department of Population Health Sciences, University of Wisconsin, Madison, Wisconsin; 3 H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida; 4 Departments of Community & Family Medicine and Pediatrics, Dartmouth Medical School, Norris Cotton Cancer Center, Lebanon, New Hamsphire; and 5 Fred Hutchinson Cancer Research Center, Seattle, Washington

Requests for reprints: Amy Trentham-Dietz, Room 307, University of Wisconsin Comprehensive Cancer Center, WARF Building, 610 Walnut Street, Madison, WI 53726. Phone: 608-263-1946; Fax: 608-265-5330. E-mail: trentham{at}wisc.edu

There is some indication that oral contraceptive use may be associated with a small increase in risk of invasive breast cancer; however, oral contraceptive use in relation to breast carcinoma in situ (BCIS) has rarely been studied. We investigated oral contraceptive use in relation to risk of BCIS in a large population-based case-control study. Female residents of Wisconsin, Massachusetts, and New Hampshire aged 20 to 74 years with a new diagnosis of BCIS (n = 1,878) were identified from statewide tumor registries in 1997 to 2001. Age-matched female controls (n = 8,041) were randomly selected from population lists. Information on oral contraceptive use and other risk factors was collected during structured telephone interviews. Odds ratios (OR) and 95% confidence intervals (95% CI) were estimated using logistic regression. In multivariate models, ever use of oral contraceptives was associated with a small and marginally significant increase in BCIS overall (OR, 1.11; 95% CI, 0.99-1.25) and for ductal carcinoma in situ (OR, 1.15; 95% CI, 1.01-1.31). No strong associations were detected according to age started, duration, time since first or last use, or oral contraceptive use relative to the first full-term pregnancy. The slightly increased risk of BCIS seemed limited to former users (OR, 1.13; 95% CI, 1.00-1.27) and women without a family history of breast cancer (OR, 1.16; 95% CI, 1.01-1.32 for ever versus never use). Consistent with invasive breast cancer, these results suggest that oral contraceptive use is at most a minor contributor to BCIS risk. (Cancer Epidemiol Biomarkers Prev 2007;16(11):2262–9)







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Molecular Cancer Research Cancer Prevention Research
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2007 by the American Association for Cancer Research.