Department of Urology, The First Affiliated Hospital of Nanchang University, Nanchang, 330000, Jiangxi Province, People's Republic of China.
Drug Des Devel Ther. 2021 Feb 16;15:639-649. doi: 10.2147/DDDT.S291369. eCollection 2021.
Gonadotropin-releasing hormone (GnRH) receptor agonists are still the most commonly used androgen deprivation treatment (ADT) drugs for prostate cancer in clinical practice. Currently, the GnRH receptor antagonists used for endocrine therapy for prostate cancer primarily include degarelix and relugolix (TAK-385). The former is administered by subcutaneous injection, while the latter is an oral drug. Compared to GnRH agonists, GnRH antagonists reduce serum testosterone levels more rapidly without an initial testosterone surge or subsequent microsurges. This review focuses on the mechanism of action of GnRH antagonists and agonists, the developmental history of GnRH antagonists, and emerging data from clinical studies of the two antagonists used as endocrine therapy for prostate cancer.
促性腺激素释放激素(GnRH)受体激动剂仍然是临床实践中最常用于前列腺癌的去雄激素治疗(ADT)药物。目前,用于前列腺癌内分泌治疗的 GnRH 受体拮抗剂主要包括地加瑞克和曲普瑞林(TAK-385)。前者通过皮下注射给药,而后者是一种口服药物。与 GnRH 激动剂相比,GnRH 拮抗剂可更快速地降低血清睾酮水平,没有初始的睾酮激增或随后的微激增。本综述重点介绍了 GnRH 拮抗剂和激动剂的作用机制、 GnRH 拮抗剂的发展历史,以及作为前列腺癌内分泌治疗的两种拮抗剂的临床研究的新数据。