Walker K J, Turkes A O, Turkes A, Zwink R, Beacock C, Buck A C, Peeling W B, Griffiths K
J Endocrinol. 1984 Nov;103(2):R1-4. doi: 10.1677/joe.0.103r001.
Twenty two patients with advanced carcinoma of the prostate have been treated for up to 3 months with the slow-release (depot) formulation of the luteinizing hormone-releasing hormone (LHRH) agonist ICI 118630. Patients were randomized to receive one of three different doses of ICI 118630 of 0.9, 1.8 or 3.6 mg. The depot preparation was injected subcutaneously every 4 weeks. At the highest dose, the concentration of testosterone in serum was significantly reduced to castrate values after 2-3 weeks of therapy. The smaller doses of ICI 118630 (1.8 or 0.9 mg every 4 weeks) similarly reduced serum testosterone concentrations although, at the lowest dose, testosterone values were not suppressed in all patients during the first month. Hormonal changes were accompanied by subjective clinical improvement in symptomatic patients and there were no significant side effects. The data clearly demonstrate the considerable therapeutic potential of ICI 118630 in the depot formulation for the treatment of advanced carcinoma of the prostate.
22例晚期前列腺癌患者接受了黄体生成素释放激素(LHRH)激动剂ICI 118630的缓释(长效)制剂治疗,疗程长达3个月。患者被随机分为三组,分别接受0.9、1.8或3.6毫克三种不同剂量的ICI 118630。长效制剂每4周皮下注射一次。在最高剂量时,治疗2至3周后血清睾酮浓度显著降低至去势水平。较小剂量的ICI 118630(每4周1.8或0.9毫克)同样降低了血清睾酮浓度,不过在最低剂量时,第一个月并非所有患者的睾酮值都受到抑制。激素变化伴随着有症状患者主观临床症状的改善,且无明显副作用。数据清楚地表明,ICI 118630长效制剂在治疗晚期前列腺癌方面具有相当大的治疗潜力。