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Volume 123, Issue 1, Pages 87.e1-87.e6 (January 2010)


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Care of the Cancer Survivor: Metabolic Syndrome after Hormone-Modifying Therapy

Amanda J. Redig, PhDabCorresponding Author Informationemail address, Hidayatullah G. Munshi, MDbc

Abstract 

Emerging evidence implicates metabolic syndrome as a long-term cancer risk factor but also suggests that certain cancer therapies might increase patients' risk of developing metabolic syndrome secondary to cancer therapy. In particular, breast cancer and prostate cancer are driven in part by sex hormones; thus, treatment for both diseases is often based on hormone-modifying therapy. Androgen suppression therapy in men with prostate cancer is associated with dyslipidemia, increasing risk of cardiovascular disease, and insulin resistance. Anti-estrogen therapy in women with breast cancer can affect lipid profiles, cardiovascular risk, and liver function. As the number of cancer survivors continues to grow, treating physicians must be aware of the potential risks facing patients who have been treated with either androgen suppression therapy or anti-estrogen therapy so that early diagnosis and intervention can be achieved.

a Feinberg School of Medicine, Northwestern University, Chicago, Ill

b Division of Hematology/Oncology, Department of Medicine and the Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, Ill

c The Jesse Brown VA Medical Center, Chicago, Ill

Corresponding Author InformationReprint requests should be addressed to Amanda J. Redig, PhD, Robert H. Lurie Comprehensive Cancer Center, 303 East Superior Street, Lurie 3-220, Chicago, IL 60611

 Funding: This work was supported by a National Institutes of Health predoctoral fellowship F30ES015668 (to A.J.R.) and grant R01CA126888 from the National Cancer Institute and a Merit grant award from the Department of Veterans Affairs (to H.G.M.).

 Conflict of Interest: Neither author has any conflicts of interest associated with the work presented in this manuscript.

 Authorship: Both authors had access to the data and played a role in writing this manuscript.

PII: S0002-9343(09)00685-8

doi:10.1016/j.amjmed.2009.06.022


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