Baumann C K, Castiglione-Gertsch M
Clinic and Policlinic for Medical Oncology, University Hospital, Bern, Switzerland.
Minerva Ginecol. 2009 Dec;61(6):517-39.
Selective estrogen receptor modulators (SERMs) and selective estrogen down regulators (SERDs) act as estrogen receptor (ER) agonists or antagonist depending on the targeted tissue and the specific configuration of the used SERM or SERD. Effects on bone, endometrium and breast cancer are of interest. Endocrine treatments have been used in breast cancer since the end of the 19th century. In the second part of the last century different compound of SERMs and SERDs have been developed and we will discuss them mainly as used in the treatment and prevention of breast cancer. Tamoxifen is the widely investigated and most used representative of these drugs and has been introduced in the advanced disease, in the neoadjuvant and adjuvant setting and for prevention of the disease. Its role has been challenged in the last years by the introduction of third generation aromatase inhibitors that have proven a higher activity than tamoxifen and a different toxicity pattern. Several other SERMs have been investigated, but none of them was clearly superior to tamoxifen. The main interest in different SERMs has to be seen in the slightly different safety profile between the different compounds. SERDs act as pure estrogen antagonist. They have been used in the treatment of advanced breast cancers and their role in other settings still needs further investigation. The increased use of aromatase inhibitors as first line endocrine therapy raises new questions on the role that tamoxifen and other SERMs or SERDs may play in breast cancer. The sequencing of endocrine therapies and the combination of endocrine therapies with new targeted therapies in hormone sensitive breast cancer remains a very important research issue. Polymorphisms in genes coding for tamoxifen metabolizing enzymes, as for instance, the CYP2D6 genotype, have the potential of becoming clinically useful predictive marker for tamoxifen response. With this meaningful newer knowledge it is possible that the place of tamoxifen in the treatment of breast cancer will be redefined in the future.
选择性雌激素受体调节剂(SERM)和选择性雌激素下调剂(SERD)根据靶向组织以及所用SERM或SERD的特定构型,可作为雌激素受体(ER)激动剂或拮抗剂。它们对骨骼、子宫内膜和乳腺癌的影响备受关注。自19世纪末以来,内分泌治疗就已应用于乳腺癌治疗。上世纪后半叶,不同的SERM和SERD化合物相继研发出来,我们将主要讨论它们在乳腺癌治疗和预防中的应用。他莫昔芬是这类药物中研究广泛且使用最多的代表药物,已被用于晚期疾病、新辅助治疗和辅助治疗以及疾病预防。近年来,第三代芳香化酶抑制剂的出现对其作用提出了挑战,这些抑制剂已被证明比他莫昔芬具有更高的活性和不同的毒性模式。人们还研究了其他几种SERM,但没有一种明显优于他莫昔芬。不同SERM的主要关注点在于不同化合物之间略有差异的安全性。SERD作为纯雌激素拮抗剂,已被用于晚期乳腺癌的治疗,其在其他治疗环境中的作用仍需进一步研究。芳香化酶抑制剂作为一线内分泌治疗的使用增加,引发了关于他莫昔芬和其他SERM或SERD在乳腺癌中可能发挥的作用的新问题。激素敏感性乳腺癌内分泌治疗的顺序以及内分泌治疗与新的靶向治疗的联合,仍然是一个非常重要的研究问题。例如,编码他莫昔芬代谢酶的基因多态性,如CYP2D6基因型,有可能成为预测他莫昔芬反应的临床有用标志物。有了这些有意义的新知识,未来他莫昔芬在乳腺癌治疗中的地位可能会被重新定义。