Bundred Nigel J
University Hospital of South Manchester, Education and Research Centre, Wythenshawe, Manchester, UK.
Curr Opin Obstet Gynecol. 2009 Feb;21(1):60-7. doi: 10.1097/GCO.0b013e32831da80e.
Aromatase inhibitors improve survival in breast cancer patients but adversely affect bone health.
Hormone receptor positive breast cancer is increasingly targeted with chemotherapy, ovarian suppression and the use of aromatase inhibitors. Aromatase inhibitors block oestrogen production in peripheral tissues and the three third generation aromatase inhibitors (anastrozole, letrozole and exemestane) reduce circulating oestrogen levels, leading to accelerated bone loss and an increased risk of fracture.The majority of fractures occur in osteopaenic women prescribed aromatase inhibitors. Current guidelines advocate bone mineral density (BMD) measurement in all patients on aromatase inhibitors with selective use of antiresorptive therapy in osteoporotic (T-score > -2.5) women. Risk factors for premature bone loss and fracture include a low BMI, family history or personal history of fragility fracture after the age of 50, oral corticosteroid use more than 6 months and cigarette smoking. Emerging evidence supports concomitant use of bisphosphonates in all women on aromatase inhibitors to prevent fracture and breast cancer recurrence.
The increasing use of aromatase inhibitors requires selection of patients for antiresorptive therapy and careful bone health management to reduce bone loss and prevent fragility fractures.
芳香化酶抑制剂可提高乳腺癌患者的生存率,但会对骨骼健康产生不利影响。
激素受体阳性乳腺癌越来越多地采用化疗、卵巢抑制和芳香化酶抑制剂进行治疗。芳香化酶抑制剂可阻断外周组织中的雌激素生成,三种第三代芳香化酶抑制剂(阿那曲唑、来曲唑和依西美坦)可降低循环雌激素水平,导致骨质流失加速和骨折风险增加。大多数骨折发生在服用芳香化酶抑制剂的骨质疏松女性患者中。当前指南提倡对所有服用芳香化酶抑制剂的患者进行骨密度(BMD)测量,并对骨质疏松(T评分>-2.5)女性患者选择性地使用抗吸收治疗。骨质过早流失和骨折的风险因素包括低体重指数、50岁后脆性骨折的家族史或个人史、口服皮质类固醇超过6个月以及吸烟。新出现的证据支持所有服用芳香化酶抑制剂的女性同时使用双膦酸盐,以预防骨折和乳腺癌复发。
芳香化酶抑制剂的使用日益增多,这就需要选择适合抗吸收治疗的患者,并进行细致的骨骼健康管理,以减少骨质流失并预防脆性骨折。