Buzdar A U, Hortobagyi G
The University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.
Clin Cancer Res. 1998 Mar;4(3):527-34.
The choice of endocrine agent for breast cancer depends on the menopausal status of the patient, the stage of disease, prognostic factors, and the toxicity profile of the agent. Endocrine therapies are typically given sequentially, with the least toxic therapy given first. Tamoxifen is considered first-line endocrine therapy for all stages of breast cancer. New antiestrogens in development include nonsteroidal agents related to tamoxifen and pure steroidal antiestrogens. Luteinizing hormone-releasing hormone agonists are an effective form of endocrine therapy for premenopausal women with advanced breast cancer, and aromatase inhibitors are effective in postmenopausal women. Newer and more selective aromatase inhibitors that are p.o. active and have improved side-effect profiles have been developed. Recent trials have found these agents to improve survival in comparison to the progestins; thus, aromatase inhibitors are replacing progestins as second-line therapy for metastatic disease. Current trials are examining the potential role of aromatase inhibitors as first-line therapy for metastatic disease or as adjuvant therapy for early disease. The antiprogestins and antiandrogens studied thus far have had only limited success in breast cancer clinical trials.
乳腺癌内分泌治疗药物的选择取决于患者的绝经状态、疾病分期、预后因素以及药物的毒性特征。内分泌治疗通常按顺序进行,先给予毒性最小的治疗。他莫昔芬被认为是各期乳腺癌的一线内分泌治疗药物。正在研发的新型抗雌激素药物包括与他莫昔芬相关的非甾体类药物和纯甾体类抗雌激素药物。促黄体生成素释放激素激动剂是晚期乳腺癌绝经前女性有效的内分泌治疗形式,芳香化酶抑制剂对绝经后女性有效。已研发出更新、更具选择性且口服有效的芳香化酶抑制剂,其副作用也有所改善。近期试验发现,与孕激素相比,这些药物可提高生存率;因此,芳香化酶抑制剂正在取代孕激素成为转移性疾病的二线治疗药物。目前的试验正在研究芳香化酶抑制剂作为转移性疾病一线治疗或早期疾病辅助治疗的潜在作用。迄今为止,所研究的抗孕激素和抗雄激素药物在乳腺癌临床试验中仅取得了有限的成功。