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Originally published as JCO Early Release 10.1200/JCO.2007.15.7123 on October 6 2008

Journal of Clinical Oncology, Vol 26, No 32 (November 10), 2008: pp. 5227-5232
© 2008 American Society of Clinical Oncology.

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*Breast Cancer
*Fractures
*Osteoporosis
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*TAMOXIFEN
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Tamoxifen Use and Osteoporotic Fracture Risk: A Population-Based Analysis

Andrew L. Cooke, Colleen Metge, Lisa Lix, Heather J. Prior, William D. Leslie

From the CancerCare Manitoba and Department of Radiology; Faculty of Pharmacy; Manitoba Centre for Health Policy, Department of Community Health Sciences, Faculty of Medicine; and the Department of Internal Medicine, University of Manitoba, Winnipeg, Canada

Corresponding author: Andrew L. Cooke, MD, CancerCare Manitoba, 675 McDermot Ave, Winnipeg Manitoba Canada, R3E 0V9; e-mail: andrew.cooke{at}cancercare.mb.ca

Purpose Although tamoxifen has been shown to increase bone mineral density in clinical trials, it is less clear whether this significantly affects fracture rates. Even fewer data are available on skeletal outcomes when tamoxifen is used outside of the context of a clinical trial. A population-based case-control study was undertaken to determine whether tamoxifen use is associated with osteoporotic fractures in routine clinical practice.

Patients and Methods Population-based administrative data for the Province of Manitoba, Canada, were examined for tamoxifen use and nontraumatic fracture codes in women 50 years of age or older. Women with osteoporotic fractures (vertebral, wrist or hip; n = 11,096) from 1996 to 2004 were each compared with three controls without fracture, matched for age, ethnicity, and comorbidity (n = 33,209). Tamoxifen use was classified as never, past use, or current use.

Results Lower osteoporotic fracture rates were associated with current tamoxifen use (univariate odds ratio [OR] = 0.68; 95% CI, 0.55 to 0.84). After controlling for demographic and medical diagnoses known to affect fracture risk, current use was associated with a significantly reduced overall osteoporotic fracture risk (adjusted OR = 0.68; 95% CI, 0.55 to 0.88) and of hip fractures (adjusted OR = 0.47; 95% CI, 0.28 to 0.77). Neither recent nor remote past tamoxifen use was associated with reduced osteoporotic fracture risk. Breast cancer was not independently associated with osteoporotic fractures (adjusted OR = 0.95; 95% CI, 0.81 to 1.12).

Conclusion In a population-based case-control study, current tamoxifen use was associated with a substantial reduction in osteoporotic fractures.

published online ahead of print at www.jco.org on October 6, 2008.

Supported by a research grant from the Canadian Institutes for Health Research.

The results and conclusions in this article are those of the authors. No official endorsement by Manitoba Health is intended or should be inferred.

Authors’ disclosures of potential conflicts of interest and author contributions are found at the end of this article.


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Copyright © 2008 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
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