The estrogenic activity of tamoxifen on the uterus increases the risk of developing benign and malignant uterine pathologies in breast cancer patients receiving this drug. This has led to gynecological interventions specifically in symptomatic women to exclude malignant disease. Given this known side effect associated with tamoxifen therapy, newer endocrine therapies such as the third-generation aromatase inhibitors have been compared to tamoxifen also in terms of their uterine effects. To date, studies that have directly compared the uterine effects of tamoxifen with that of aromatase inhibitors generally show that aromatase inhibitors such as anastrozole, letrozole, and exemestane are associated with less uterine pathologies compared to tamoxifen. Furthermore, aromatase inhibitors may even reverse uterine abnormalities induced by tamoxifen. This implies that the absence of a stimulatory effect on the uterus would be one of the benefits gained with aromatase inhibitor therapy and may decrease or even obviate the need for gynecological interventions.

译文

:他莫昔芬对子宫的雌激素活性增加了接受这种药物的乳腺癌患者发生良性和恶性子宫病变的风险。这导致专门针对有症状妇女的妇科干预措施,以排除恶性疾病。考虑到与他莫昔芬疗法有关的已知副作用,就其子宫作用而言,已将较新的内分泌疗法(如第三代芳香化酶抑制剂)与他莫昔芬进行了比较。迄今为止,直接将他莫昔芬与芳香酶抑制剂的子宫作用进行比较的研究通常显示,与他莫昔芬相比,芳香酶抑制剂(例如阿那曲唑,来曲唑和依西美坦)与子宫病变的发生率相关。此外,芳香酶抑制剂甚至可以逆转他莫昔芬引起的子宫异常。这意味着缺乏对子宫的刺激作用将是芳香化酶抑制剂治疗所获得的好处之一,并且可能减少甚至消除对妇科干预的需求。

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