Department of Urology & Paris 7 University, APHP, Saint-Louis Hospital, Paris, France.
Future Oncol. 2013 Jan;9(1):93-102. doi: 10.2217/fon.12.158.
Among the therapies to achieve medical castration, gonadotropin-releasing hormone (GnRH) agonists have better safety profiles than estrogens and anti-androgens. In addition, slow-release formulations of GnRH agonists offer patients flexibility, improve quality of life and eventually reduce cost. To illustrate the role of medical castration in prostate cancer, this paper reviews data on the GnRH agonist triptorelin long-duration and shorter-duration formulations. A similar proportion of patients achieved and maintained castration levels of serum testosterone (≤50 ng/dl) with all triptorelin formulations. Moreover, using a stricter definition of medical castration (serum testosterone <20 ng/dl), castration was maintained in >90% of patients with the 6-month triptorelin formulation. The new formulation was also well-tolerated, whilst being more convenient for patients. This short review assesses the role of this GnRH agonist in the treatment of prostate cancer.
在实现医学去势的治疗方法中,促性腺激素释放激素(GnRH)激动剂比雌激素和抗雄激素具有更好的安全性。此外, GnRH 激动剂的缓释制剂为患者提供了更大的灵活性,提高了生活质量,并最终降低了成本。为了说明医学去势在前列腺癌中的作用,本文综述了 GnRH 激动剂曲普瑞林长程和短程制剂的数据。所有曲普瑞林制剂的患者都达到并维持了血清睾酮(≤50ng/dl)的去势水平。此外,使用更严格的医学去势定义(血清睾酮<20ng/dl),90%以上的患者使用 6 个月的曲普瑞林制剂维持去势。新制剂也具有良好的耐受性,同时对患者更加方便。这篇简短的综述评估了这种 GnRH 激动剂在前列腺癌治疗中的作用。