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晚期乳腺癌的激素治疗

Hormonal treatment of advanced breast cancer.

作者信息

Tellez C, Jordan V C

机构信息

Northwestern University Medical School, Chicago, Illinois, USA.

出版信息

Surg Oncol Clin N Am. 1995 Oct;4(4):751-77.

PMID:8535909
Abstract

Endocrine therapy for breast cancer has been used for almost a century, but because of the enormous success of tamoxifen there has been a resurgence of interest by the pharmaceutical industry to develop new and innovative endocrine therapies. Overall, the strategy is quite simple. Estrogen stimulates growth; therefore, the goal is to deny the breast tumor estrogens. Tamoxifen accomplishes this by blocking the estrogen receptor. The new antiestrogens, toremifene and droloxifene, however, appear to have no greater activity than tamoxifen in the treatment of advanced disease and therefore may ultimately offer no advantages over current therapy. In contrast, the pure antiestrogens hold additional promise as they may produce a more profound inhibitory effect on the tumor, and the response may be maintained longer. An orally active, pure antiestrogen, however, would be an important advance. The strategy of using GnRH agonists for premenopausal patients clearly has merit to produce a chemical oophorectomy. The strategy could be integrated into the general treatment plan for the young premenopausal patient taking tamoxifen who may not have had her menstrual cycles stopped by combination chemotherapy. The GnRH agonists would block the reflex rise in estradiol caused by tamoxifen therapy and ultimately produce a more efficient antihormonal therapy. Indeed, the different specific aromatase inhibitors can also be integrated into the treatment plan to produce a complete estrogen blockade. Whether the use will be found to be superior to pure antiestrogens, however, must await the completion of comparative clinical studies. If all the results of endocrine therapy are therapeutically similar, the final strategy may depend on the acceptability by the patient of an individual delivery method for each pharmaceutical approach.

摘要

乳腺癌内分泌治疗已应用了近一个世纪,但由于他莫昔芬取得了巨大成功,制药行业对开发新型内分泌治疗方法的兴趣再度兴起。总体而言,策略相当简单。雌激素刺激生长,因此目标是阻断乳腺肿瘤的雌激素供应。他莫昔芬通过阻断雌激素受体来实现这一目标。然而,新型抗雌激素药物托瑞米芬和屈洛昔芬在治疗晚期疾病方面似乎并不比他莫昔芬更具活性,因此最终可能并不比现有疗法更具优势。相比之下,纯抗雌激素药物更具前景,因为它们可能对肿瘤产生更显著的抑制作用,且疗效维持时间可能更长。然而,一种口服活性的纯抗雌激素药物将是一项重要进展。对于绝经前患者使用促性腺激素释放激素(GnRH)激动剂以实现化学去势的策略显然具有价值。该策略可纳入年轻绝经前患者接受他莫昔芬治疗的总体治疗方案中,这些患者可能未因联合化疗而停经。GnRH激动剂可阻断他莫昔芬治疗引起的雌二醇反射性升高,最终产生更有效的抗激素治疗。实际上,不同的特异性芳香化酶抑制剂也可纳入治疗方案以实现完全的雌激素阻断。然而,其使用是否优于纯抗雌激素药物,必须等待比较临床研究的完成。如果所有内分泌治疗结果在治疗效果上相似,最终策略可能取决于患者对每种药物治疗方法的个体给药方式的接受程度。

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