Nesković-Konstantinović Z, Radulović S, Vuletić L
Institut za onkologiju i radiologiju, Beograd.
Srp Arh Celok Lek. 1993 Jan-Feb;121(1-2):33-5.
The recent data about the treatment of advanced breast cancer patients with synthetic LH-RH analogues are presented. Although synthetized 20 years ago, the agonistic analogues of LH-RH were introduced in clinical oncology recently. The inhibition of pituitary and gonadal function that occurs after chronic administration of agonists of LH-RH, with the creation of a sex steroid deprivation and elimination of stimulatory effects of oestrogen or testosterone, is the basis for their application in oncology. In advanced breast cancer patients they successfully replace surgical or radiological castration. The main advantage of medical castration is reversibility. However, the discovery of the specific LH-RH receptors effect on mammary tumor membranes as well as on some other tumor cells, suggested the possible direct antitumor effect of LH-RH agonists. This finding enlarge the oncological application of LH-RH agonistic analogues.
本文介绍了近期关于使用合成促黄体生成素释放激素(LH-RH)类似物治疗晚期乳腺癌患者的数据。尽管LH-RH激动剂类似物在20年前就已合成,但直到最近才被引入临床肿瘤学领域。长期使用LH-RH激动剂后,垂体和性腺功能受到抑制,导致性类固醇缺乏,雌激素或睾酮的刺激作用消除,这是其在肿瘤学中应用的基础。在晚期乳腺癌患者中,它们成功地替代了手术去势或放射去势。药物去势的主要优点是可逆性。然而,研究发现LH-RH特异性受体对乳腺肿瘤细胞膜以及其他一些肿瘤细胞有作用,提示LH-RH激动剂可能具有直接抗肿瘤作用。这一发现扩大了LH-RH激动剂类似物在肿瘤学中的应用。