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首页> 外文期刊>Mini reviews in medicinal chemistry >Aromatase inhibitors: a new reality for the adjuvant endocrine treatment of early-stage breast cancer in postmenopausal women.
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Aromatase inhibitors: a new reality for the adjuvant endocrine treatment of early-stage breast cancer in postmenopausal women.

机译:芳香酶抑制剂:绝经后妇女辅助内分泌治疗早期乳腺癌的新现实。

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Tamoxifen, a selective estrogen receptor modulator (SERM), has been used for many decades as the "gold standard" adjuvant treatment for patients with hormone-receptor-positive early breast cancer. This drug, when administered for 5 years, reduces the risk for recurrence, contralateral breast cancer (BC) and death. The optimal duration of tamoxifen in the adjuvant setting has not been established yet, but it has been demonstrated that 5 years are better than shorter treatment while it is still unclear if a prolongation of the treatment for more than 5 years is worthwhile. In the last few years, third generation aromatase inhibitors (AIs), either steroidal (exemestane) or non-steroidal (anastrozole, letrozole), have shown to be an effective alternative to tamoxifen in postmenopausal patients with BC regardless of its stage. These agents act by blocking the aromatase enzyme which converts androgens into estrogens. The goal of this article was to review the results of recent randomized trials comparing AIsto tamoxifen in postmenopausal women in the adjuvant setting. Two strategies have been utilized: a direct upfront comparison in which both tamoxifen and AIs were given for 5 years or an early switch in which AIs were administered after 2-3 years of tamoxifen for 3-2 years or vice versa. Both strategies have shown a superiority of AIs over tamoxifen and a different safety profile but, the optimal treatment modality has yet to be defined. Moreover, in an attempt to further reduce patients' risk of recurrence after the administration of tamoxifen for 5 years, three trials have evaluated the role of prolonging the adjuvant treatment with AIs for 5 more years in comparison to placebo (late switch). A significant improvement of disease-free survival and of overall survival in the subgroup of node-positive patients, at least in one trial, has been observed with AIs. Despite these important results several unanswered questions remain and the results of ongoing trials will hopefully clarify some of them.
机译:他莫昔芬是一种选择性雌激素受体调节剂(SERM),已作为激素受体阳性早期乳腺癌患者的“黄金标准”辅助治疗方法使用了数十年。服用5年后,该药可降低复发,对侧乳腺癌(BC)和死亡的风险。他莫昔芬在辅助治疗中的最佳持续时间尚未确定,但已证明5年比短期治疗更好,而尚不清楚延长5年以上的治疗是否值得。在过去的几年中,无论绝经后的BC患者分期如何,甾体(依西美坦)或非甾体(阿那曲唑,来曲唑)第三代芳香化酶抑制剂(AIs)均可作为他莫昔芬的有效替代品。这些试剂通过阻断将雄激素转化为雌激素的芳香化酶起作用。本文的目的是审查最近的随机试验的结果,该试验比较了AIsto他莫昔芬在辅助治疗中绝经后妇女中的作用。已经采用了两种策略:直接的前期比较(其中他莫昔芬和AIs均给予5年)或早期转换(其中在他莫昔芬2-3年后3-2年内给予AI),反之亦然。两种策略均显示出AI优于他莫昔芬和不同的安全性,但尚不确定最佳治疗方式。此外,为了进一步降低患者服用他莫昔芬5年后的复发风险,与安慰剂相比,三项试验评估了将AIs辅助治疗延长5年的作用。至少在一项试验中,使用AI可以观察到淋巴结阳性患者亚组的无病生存率和总体生存率显着提高。尽管取得了这些重要的结果,但仍有一些悬而未决的问题,正在进行的试验结果有望澄清其中的一些问题。

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