Palacios Santiago
Palacios Institute of Women's Health, Antonio Acuña 9, 28009 Madrid, Spain.
Menopause Int. 2007 Mar;13(1):27-34. doi: 10.1258/175404507780456791.
Selective estrogen receptor modulators (SERMs) are compounds that display mixed estrogen agonist/antagonist activity. Currently, four SERMs are licensed for clinical use: tamoxifen, toremifene, clomifene and raloxifene. The STAR and RUTH trials have provided useful data about the potential role of SERMs in the primary prevention of breast cancer and cardiovascular disease in postmenopausal women. New-generation SERMs, such as bazedoxifene, arzoxifene, lasofoxifene and ospemifene, are currently being evaluated. The aim is to find a SERM that conserves the skeleton and prevents breast cancer without increasing the risk of endometrial cancer and venous thromboembolism, and without inducing hot flushes. Technological advances in the study of estrogen receptor activation will provide key information for drug development.
选择性雌激素受体调节剂(SERM)是一类具有混合雌激素激动剂/拮抗剂活性的化合物。目前,有四种SERM被批准用于临床:他莫昔芬、托瑞米芬、氯米芬和雷洛昔芬。STAR和RUTH试验提供了关于SERM在绝经后女性乳腺癌和心血管疾病一级预防中潜在作用的有用数据。新一代SERM,如巴多昔芬、阿佐昔芬、拉索昔芬和奥司米芬,目前正在评估中。目标是找到一种既能保护骨骼又能预防乳腺癌,同时不增加子宫内膜癌和静脉血栓栓塞风险,且不会引起潮热的SERM。雌激素受体激活研究的技术进步将为药物开发提供关键信息。