Buzdar Aman U
Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Semin Oncol. 2003 Oct;30(5 Suppl 16):21-9. doi: 10.1053/j.seminoncol.2003.08.004.
For the past 25 years tamoxifen has been the mainstay for adjuvant treatment of postmenopausal patients with hormone-sensitive breast cancer. However, tamoxifen has some safety and tolerability issues, and its partial estrogen-receptor agonist activity may have efficacy implications. Highly specific aromatase inhibitors, of which anastrozole was the first, were introduced in the 1990s and have emerged as a potentially better tolerated and more effective class of agents targeting hormonally responsive breast cancer. This article provides a review of the clinical pharmacology of anastrozole (1 mg once daily) and reviews the first results of the ongoing Arimidex, Tamoxifen, Alone or in Combination early breast cancer trial, initiated in 1996. This randomized, double-blind multicenter trial compared tamoxifen (20 mg once daily) with anastrozole (1 mg once daily) alone and the combination of anastrozole plus tamoxifen, as adjuvant endocrine treatment for postmenopausal patients with operable, invasive, early breast cancer. The results of the Arimidex, Tamoxifen, Alone or in Combination trial show anastrozole to be an effective and well tolerated endocrine option for early breast cancer and provide evidence for its potential role in chemoprevention.
在过去25年里,他莫昔芬一直是绝经后激素敏感性乳腺癌患者辅助治疗的主要药物。然而,他莫昔芬存在一些安全性和耐受性问题,其部分雌激素受体激动剂活性可能对疗效有影响。高特异性芳香化酶抑制剂(阿那曲唑是其中首个药物)于20世纪90年代问世,并已成为一类针对激素反应性乳腺癌、耐受性可能更好且更有效的药物。本文对阿那曲唑(每日1次,每次1 mg)的临床药理学进行了综述,并回顾了始于1996年的“阿那曲唑、他莫昔芬单药或联合应用”早期乳腺癌试验的首批结果。这项随机、双盲多中心试验将他莫昔芬(每日1次,每次20 mg)与阿那曲唑(每日1次,每次1 mg)单药以及阿那曲唑加他莫昔芬联合用药进行比较,作为绝经后可手术的浸润性早期乳腺癌患者的辅助内分泌治疗。“阿那曲唑、他莫昔芬单药或联合应用”试验结果表明,阿那曲唑是早期乳腺癌一种有效且耐受性良好的内分泌治疗选择,并为其在化学预防中的潜在作用提供了证据。