Iversen P, Tveter K, Varenhorst E
Department of Urology, University of Copenhagen, Rigshospitalet, Denmark.
Scand J Urol Nephrol. 1996 Apr;30(2):93-8. doi: 10.3109/00365599609180896.
The effect of Casodex (ICI 176,334), a new, once-daily, selective antiandrogen, given as 50 mg monotherapy, was compared with orchidectomy in a randomised, multicentre, open study in 376 patients with metastatic prostate cancer. At 3 months, PSA was reduced by 86% in the Casodex group and by 96% in the orchidectomy group. Treatment failed in 51 patients in the orchidectomy group and 66 showed a subjective response. Treatment failed in 86 patients treated with Casodex and 40 patients showed a subjective response. Patients treated with Casodex maintained their sexual interest better than those in the orchidectomy group. Median survival was significantly longer in the orchidectomy group. Casodex was well-tolerated. The most likely reason for the differences between the groups regarding time to treatment failure and survival is that the dose of Casodex was too small. Further studies with higher doses of Casodex are in progress.
在一项针对376例转移性前列腺癌患者的随机、多中心、开放性研究中,将新型每日一次选择性抗雄激素药物康士得(ICI 176,334)50mg单药治疗的效果与睾丸切除术进行了比较。3个月时,康士得组前列腺特异性抗原(PSA)降低了86%,睾丸切除组降低了96%。睾丸切除组有51例患者治疗失败,66例有主观反应。接受康士得治疗的患者中有86例治疗失败,40例有主观反应。接受康士得治疗的患者比睾丸切除组患者更好地维持了性兴趣。睾丸切除组的中位生存期显著更长。康士得耐受性良好。两组在治疗失败时间和生存期方面存在差异的最可能原因是康士得的剂量过小。更高剂量康士得的进一步研究正在进行中。