Hadji Peyman
University Hospital for Obstetrics and Gynecology, Philipps-University of Marburg, Germany.
Breast Care (Basel). 2010;5(5):290-296. doi: 10.1159/000321426. Epub 2010 Oct 19.
Postmenopausal women are at an increased risk of osteopenia and osteoporosis due to the physiologic loss of the bone protective effects of estrogen. Additionally, disease-related risk factors also contribute to the increased fracture risk. To further complicate matters, one of the most common and severe safety issues associated with cancer therapies for breast cancer patients is bone loss and the associated increased risk of fractures. These facts underscore the need to carefully monitor bone mineral density in patients with endocrine-responsive breast cancer, and to consider adjuvant therapy that may help manage and/or prevent bone loss and fracture. Aromatase inhibitors (AIs) are now in widespread clinical use for women with hormone receptor-positive breast cancer and have replaced tamoxifen as the gold standard of care. AIs target the estrogen biosynthetic pathway and deprive tumor cells of the growth-promoting effects of estrogen. These treatments provide significant benefit to patients in terms of improved disease-free and overall survival. Adversely, there is a concern of an increased risk of bone loss with prolonged therapy consequently leading to an increased fracture risk. This manuscript will review the recent literature pertaining to AI-associated bone loss and discuss suggested management and preventative approaches that may help patients remain on therapy to derive the most clinical benefits.
由于雌激素对骨骼的保护作用出现生理性丧失,绝经后女性患骨质减少和骨质疏松症的风险增加。此外,与疾病相关的风险因素也会导致骨折风险增加。更复杂的是,乳腺癌患者癌症治疗最常见且严重的安全问题之一是骨质流失以及随之而来的骨折风险增加。这些事实凸显了对内分泌反应性乳腺癌患者仔细监测骨矿物质密度的必要性,并考虑采用可能有助于管理和/或预防骨质流失及骨折的辅助治疗。芳香化酶抑制剂(AIs)目前在激素受体阳性乳腺癌女性患者中广泛应用于临床,并且已取代他莫昔芬成为护理的金标准。芳香化酶抑制剂作用于雌激素生物合成途径,使肿瘤细胞无法获得雌激素的促生长作用。这些治疗在改善无病生存期和总生存期方面为患者带来显著益处。不利的是,人们担心长期治疗会增加骨质流失风险,进而导致骨折风险增加。本手稿将回顾近期关于芳香化酶抑制剂相关骨质流失的文献,并讨论建议的管理和预防方法,这些方法可能有助于患者继续接受治疗以获得最大临床益处。