Goss Paul
Breast Cancer Prevention Program at the Princess Margaret Hospital, Toronto, Ontario, Canada.
Cancer Control. 2002 Mar-Apr;9(2 Suppl):2-8. doi: 10.1177/107327480200902S01.
Anti-aromatase agents now have a central role in the management of breast cancer in postmenopausal women; they are superior to megestrol acetate as second-line therapy and to tamoxifen for initial therapy of metastatic disease. They also are highly active as neoadjuvant therapy. Two classes of anti-aromatase agents are available: steroidal (eg, exemestane) and nonsteroidal (eg, anastrozole, letrozole). Although both types of agents act on the aromatase enzyme, they do so by different mechanisms and have different effects on cellular aromatase activity. Nonsteroidal agents are associated with increased aromatase enzyme content and steroidal agents are associated with decreased content. The increase in aromatase content seen with the nonsteroidal agents may in part explain the development of resistance with these agents and the ability of the steroidal agent exemestane to induce a response when nonsteroidal agents fail. Because the anti-aromatase agents almost completely eliminate endogenous estrogen production, they not only affect breast cancer tissues, but also may alter the function of other estrogen-responsive tissues. However, preclinical data show that the steroidal agent exemestane may actually improve bone and lipid metabolism. In addition, no increase in clinical fracture rate has been noted in women treated with exemestane in metastatic trials; the fracture risk has not yet been studied following prolonged exposure in healthy women. Exemestane associated beneficial effects on these end organs may be due to the steroidal nature of both the parent compound and its principal metabolite, 17-hydroexemestane. Similar benefits have not been reported with nonsteroidal antiaromatase agents. Based on their excellent activity in the metastatic setting, anti-aromatase agents are now being evaluated in the adjuvant setting and in pilot studies for chemoprevention. These studies will provide long-term data in healthy women and will help to differentiate anti-aromatase agents, in terms of their efficacy in the treatment of breast cancer and their effects on end organs.
抗芳香化酶药物目前在绝经后女性乳腺癌的治疗中发挥着核心作用;作为二线治疗药物,它们优于醋酸甲地孕酮,在转移性疾病的初始治疗中也优于他莫昔芬。它们作为新辅助治疗也具有很高的活性。有两类抗芳香化酶药物可供使用:甾体类(如依西美坦)和非甾体类(如阿那曲唑、来曲唑)。尽管这两类药物都作用于芳香化酶,但作用机制不同,对细胞芳香化酶活性的影响也不同。非甾体类药物与芳香化酶含量增加有关,而甾体类药物与含量降低有关。非甾体类药物导致的芳香化酶含量增加可能部分解释了这些药物耐药性的产生,以及当非甾体类药物失效时甾体类药物依西美坦诱导缓解的能力。由于抗芳香化酶药物几乎完全消除内源性雌激素的产生,它们不仅影响乳腺癌组织,还可能改变其他雌激素反应性组织的功能。然而,临床前数据表明,甾体类药物依西美坦实际上可能改善骨骼和脂质代谢。此外,在转移性试验中接受依西美坦治疗的女性中,未观察到临床骨折率增加;在健康女性长期使用后,骨折风险尚未得到研究。依西美坦对这些终末器官的有益作用可能归因于母体化合物及其主要代谢产物17-羟依西美坦的甾体性质。非甾体类抗芳香化酶药物尚未报告有类似益处。基于其在转移性疾病中的出色活性,抗芳香化酶药物目前正在辅助治疗和化学预防的试点研究中进行评估。这些研究将为健康女性提供长期数据,并有助于区分抗芳香化酶药物在乳腺癌治疗中的疗效及其对终末器官的影响。