Endocrine Therapy of Breast Cancer

Author(s): F. Lumachi, G. Luisetto, S. M.M. Basso, U. Basso, A. Brunello, V. Camozzi

Journal Name: Current Medicinal Chemistry

Volume 18 , Issue 4 , 2011

Become EABM
Become Reviewer
Call for Editor


Breast cancer remains one of the first leading causes of death in women, and currently endocrine treatment is of major therapeutic value in patients with estrogen-receptor positive tumors. Selective estrogen-receptor modulators (SERMs), such as tamoxifen and raloxifene, aromatase inhibitors, and GnRH agonists are the drugs of choice. Tamoxifen, a partial nonsteroidal estrogen agonist, is a type II competitive inhibitor of estradiol at its receptor, and the prototype of SERMs. Aromatase inhibitors significantly lower serum estradiol concentration in postmenopausal patients, having no detectable effects on adrenocortical steroids formation, while GnRH agonists suppress ovarian function, inducing a menopause- like condition in premenopausal women. Endocrine therapy has generally a relatively low morbidity, leading to a significant reduction of mortality for breast cancer. The aim of chemoprevention is to interfere early with the process of carcinogenesis, reducing the risk of cancer development. As preventive agents, raloxifene and tamoxifene are equivalent, while raloxifene has more potent antiresorptive effects in postmenopausal osteoporosis. Endocrine treatment is usually considered a standard choice for patients with estrogen-receptor positive cancers and non-life-threatening advanced disease, or for older patients unfit for aggressive chemotherapy regimens. Several therapeutic protocols used in patients with breast cancer are associated with bone loss, which may lead to an increased risk of fracture. Bisphosphonates are the drugs of choice to treat such a drug-induced bone disease. The aim of this review is to outline current understanding on endocrine therapy of breast cancer.

Keywords: Breast cancer, endocrine therapy, chemoprevention, adjuvant therapy, SERM, tamoxifen, raloxifene, aromatase inhibitors, estrogen-receptor positive tumors, Selective estrogen-receptor modulators, GnRH agonists, serum estradiol, postmenopausal osteoporosis., Bisphosphonates, lymph node, ovarian suppres-sive drugs, estradiol, carcinogenesis, atypical hyperplasia, ovariectomy, adrenalec-tomy, hypophysectomy, Non-steroidal anti-inflammatory drugs (NSAIDs), cyclooxygenase (COX), Early Breast Cancer Trial-ists' Collaborative Group (EBCTCG), progesterone-receptor, gonadotropin-releasing hormone (GnRH), dual-energy x-ray absorptiometry (DXA), clodronate, risedronate, ibandronate, Osteonecrosis, prophylaxis

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2011
Page: [513 - 522]
Pages: 10
DOI: 10.2174/092986711794480177
Price: $65

Article Metrics

PDF: 90