Interdisciplinary Breast Centre, Helios Klinikum Berlin-Buch, University Charité, Berlin, Germany.
Ther Clin Risk Manag. 2008 Dec;4(6):1295-304. doi: 10.2147/tcrm.s4007.
The adjuvant treatment of women with endocrine-sensitive early breast cancer has been dominated for the last 40 years by tamoxifen. However, the side-effects associated with this therapy have prompted a search for safer and biochemically more selective endocrine agents and led to the development of the third-generation aromatase inhibitors (AIs) anastrozole, letrozole and exemestane. Promising results in advanced disease have paved the way for treating early breast cancer, and AIs are increasingly replacing tamoxifen in the adjuvant setting. Several large, randomized trials with AIs have been completed or are ongoing in women with early-stage breast cancer, documenting the significant impact that these drugs are making on the risk for recurrence of breast cancer. As a result, there is increasing and widespread use of AI therapy for the treatment of early-stage endocrine-responsive breast cancer. This review summarizes the data for exemestane in the adjuvant setting, showing that a switch to exemestane after 2 to 3 years of tamoxifen therapy is associated with a statistically significant survival benefit and is regarded as being sensitive by international and national experts.
在过去的 40 年中,内分泌敏感型早期乳腺癌的辅助治疗一直以他莫昔芬为主。然而,这种治疗相关的副作用促使人们寻求更安全、生化选择性更强的内分泌药物,并导致第三代芳香酶抑制剂(AIs)阿那曲唑、来曲唑和依西美坦的发展。晚期疾病的有前景的结果为早期乳腺癌的治疗铺平了道路,AIs 正在逐渐取代辅助治疗中的他莫昔芬。在早期乳腺癌患者中已经完成或正在进行几项大型随机试验,这些试验记录了这些药物对乳腺癌复发风险的显著影响。因此,越来越多的人广泛使用 AI 治疗早期内分泌反应性乳腺癌。本综述总结了阿那曲唑在辅助治疗中的数据,表明在接受 2 至 3 年他莫昔芬治疗后转为阿那曲唑治疗与统计学上显著的生存获益相关,并被国际和国内专家认为是敏感的。