Gasco Milena, Argusti Alessandra, Bonanni Bernardo, Decensi Andrea
Division of Medical and Preventive Oncology, E.O. Ospedali Galliera, 16128 Genoa, Italy.
Eur J Cancer. 2005 Sep;41(13):1980-9. doi: 10.1016/j.ejca.2005.04.017.
Selective estrogen receptor modulators (SERMs) play a key role in breast cancer chemoprevention. Tamoxifen has been shown to reduce breast cancer incidence by 30-40% in at-risk subjects in large phase III trials. However, toxicity may be a limiting factor. Thus, different strategies are being pursued to improve the risk: benefit ratio of using these compounds in chemoprevention. Firstly, the second generation SERM raloxifene is currently undergoing evaluation in comparison with tamoxifen in a large phase III trial. Also, lower doses of tamoxifen are being assessed in phase II-III trials. In addition, the combination of hormone replacement therapy (HRT) or aromatase inhibitors and tamoxifen at low doses may reduce the risks while retaining the benefits of either agents. Finally, new agents that interfere with the onset of ER-negative breast cancer are being sought for combination chemoprevention since almost a third of breast cancers will not be sensitive to hormonal modulation.
选择性雌激素受体调节剂(SERM)在乳腺癌化学预防中起着关键作用。在大型III期试验中,他莫昔芬已被证明可使高危人群的乳腺癌发病率降低30%-40%。然而,毒性可能是一个限制因素。因此,人们正在探索不同的策略来提高在化学预防中使用这些化合物的风险效益比。首先,第二代SERM雷洛昔芬目前正在一项大型III期试验中与他莫昔芬进行对比评估。此外,II-III期试验正在评估更低剂量的他莫昔芬。另外,激素替代疗法(HRT)或芳香化酶抑制剂与低剂量他莫昔芬联合使用可能会降低风险,同时保留两种药物的益处。最后,由于近三分之一的乳腺癌对激素调节不敏感,正在寻找可干扰雌激素受体阴性乳腺癌发病的新型药物用于联合化学预防。