Medical Oncology, Baylor-Sammons Cancer Center, USA.
Medical Oncology, Baylor-Sammons Cancer Center, USA ; Texas Oncology PA, USA ; US Oncology, Dallas, TX, USA.
Breast Cancer (Dove Med Press). 2011 Oct 4;3:113-25. doi: 10.2147/BCTT.S22905.
Estrogen and its metabolites play a significant role in the proliferation of hormone receptor-positive breast cancer. In postmenopausal women, aromatase inhibitors can significantly reduce estrogen levels by blocking enzyme-mediated estrogen synthesis within tissues. Third-generation aromatase inhibitors have now surpassed tamoxifen as first-line therapy for postmenopausal women with metastatic, hormone receptor-positive, breast cancer, showing improved response rates and time to progression. Aromatase inhibitors have shown incremental improvements in disease-free survival, lower local recurrence rates, lower metastatic recurrence rates, and a lower incidence of contralateral breast cancer over tamoxifen when used in the adjuvant setting. Aromatase inhibitors are recommended to be used as adjuvant therapy within the first 5 years of hormonal therapy and may be used either upfront for 5 years or sequenced with tamoxifen. No superiority of one aromatase inhibitor over another has yet been shown. The side effect profiles of aromatase inhibitors have some key differences compared with tamoxifen. These differences may influence treatment choices as well as impact compliance.
雌激素及其代谢产物在激素受体阳性乳腺癌的增殖中发挥重要作用。在绝经后妇女中,芳香化酶抑制剂通过阻断组织内酶介导的雌激素合成,可显著降低雌激素水平。第三代芳香化酶抑制剂现已超越他莫昔芬,成为转移性、激素受体阳性乳腺癌绝经后妇女的一线治疗药物,显示出改善的缓解率和进展时间。在辅助治疗中,与他莫昔芬相比,芳香化酶抑制剂在无病生存期、局部复发率、远处转移复发率和对侧乳腺癌发生率方面均有显著改善。建议在激素治疗的前 5 年内使用芳香化酶抑制剂作为辅助治疗,可连续使用 5 年,也可与他莫昔芬序贯使用。目前尚未显示一种芳香化酶抑制剂优于另一种。与他莫昔芬相比,芳香化酶抑制剂的副作用谱存在一些关键差异。这些差异可能会影响治疗选择,并影响患者的依从性。