Estrogen deprivation therapy, also known as endocrine therapy, is a form of hormone therapy that is used in the treatment of breast cancer. Modalities include antiestrogens or estrogen blockers such as selective estrogen receptor modulators (SERMs) like tamoxifen, selective estrogen receptor degraders like fulvestrant, and aromatase inhibitors like anastrozole and ovariectomy.[citation needed]
| Estrogen deprivation therapy | |
|---|---|
| Other names | Endocrine therapy |
| Specialty | oncology |
A breast biopsy is tested for whether the cancer cells contain estrogen or progesterone receptors. A breast cancer that is positive for estrogen receptors is usually also progesterone receptor positive. This type of cancer is called ER/PR positive, which constitutes approximately 80% of all breast cancers.[1] ER positive cancers use estrogen to grow, so administering endocrine therapy to a patient diagnosed with ER/PR positive cancer will depress tumor growth.
Endocrine therapy should not be confused with menopausal hormone therapy or hormone replacement therapy, which is using estrogen and/or progesterone supplements to relieve symptoms of menopause.[2] Estrogen feeds breast cancer cells, so when a woman on hormone replacement therapy (HRT) is diagnosed with ER/PR positive breast cancer, her doctor will ask her to stop the HRT.[2]
Patients that have tumors small enough to take out with surgery will receive endocrine therapy after their surgery, which is part of adjuvant therapy. Large tumors may receive neo-adjuvant therapy via chemotherapy or radiation to shrink the tumor small enough to operate on.
Types of Endocrine Therapy Medication
editSelective Estrogen Receptor Modulators (SERMs)
editSERMs act by mimicking estrogen and replacing estrogen on estrogen receptors, blocking estrogen from binding and preventing tumors from using estrogen to grow.[2] They do not interfere with estrogen production. Tamoxifen (Nolvadex®) is a commonly used drug for pre-menopausal women diagnosed with ER/PR positive breast cancer. Tamoxifen selectively blocks the effect of estrogen in breast tissue but acts as an estrogen agonist in the uterus and in bone.[2] Research shows that women on tamoxifen for at least 5 years out of surgery are less likely to have recurrent breast cancer, including new breast cancer in the other breast, and death at 15 years.[3]
See also
editReferences
edit- ^ Kohler BA, Sherman RL, Howlader N, Jemal A, Ryerson AB, Henry KA, Boscoe FP, Cronin KA, Lake A, Noone AM, Henley SJ, Eheman CR, Anderson RN, Penberthy L (June 2015). "Annual Report to the Nation on the Status of Cancer, 1975-2011, Featuring Incidence of Breast Cancer Subtypes by Race/Ethnicity, Poverty, and State". Journal of the National Cancer Institute. 107 (6): djv048. doi:10.1093/jnci/djv048. PMC 4603551. PMID 25825511.
- ^ a b c d "Hormone Therapy for Breast Cancer". National Cancer Institute. 2017-03-03. Retrieved 2018-11-07.
- ^ Davies C, Godwin J, Gray R, Clarke M, Cutter D, Darby S, McGale P, Pan HC, Taylor C, Wang YC, Dowsett M, Ingle J, Peto R (August 2011). "Relevance of breast cancer hormone receptors and other factors to the efficacy of adjuvant tamoxifen: patient-level meta-analysis of randomised trials". Lancet. 378 (9793): 771–84. doi:10.1016/S0140-6736(11)60993-8. PMC 3163848. PMID 21802721.