Smith J A, Glode L M, Wettlaufer J N, Stein B S, Glass A G, Max D T, Anbar D, Jagst C L, Murphy G P
Urology. 1985 Feb;25(2):106-14. doi: 10.1016/0090-4295(85)90523-0.
Leuprolide is a new, potent analogue of gonadotropin-releasing hormone which, after an initial transient stimulation, causes a profound suppression of serum gonadotropins and testosterone. One hundred eighteen patients with advanced carcinoma of the prostate have undergone treatment with leuprolide in a multi-institutional trial. Minimal evidence of objective response was seen in patients who had failed prior endocrine therapy with orchiectomy or estrogens. In patients without previous hormonal treatment, leuprolide induced an objective disease response (72%) comparable to alternative primary endocrine therapy. Considering the lack of significant side effects seen with long-term GnRH agonists, compounds such as leuprolide may prove to be the preferred initial endocrine therapy for selected patients with metastatic carcinoma of the prostate.
亮丙瑞林是一种新型、强效的促性腺激素释放激素类似物,在最初的短暂刺激后,可导致血清促性腺激素和睾酮水平大幅降低。在一项多机构试验中,118例晚期前列腺癌患者接受了亮丙瑞林治疗。先前接受过睾丸切除术或雌激素内分泌治疗失败的患者,几乎没有客观缓解的证据。在未接受过激素治疗的患者中,亮丙瑞林诱导的客观疾病缓解率(72%)与其他一线内分泌治疗相当。考虑到长期使用促性腺激素释放激素激动剂未见明显副作用,亮丙瑞林等化合物可能被证明是某些转移性前列腺癌患者首选的初始内分泌治疗药物。