睾酮在去势抵抗性前列腺癌治疗中的作用

M. Drazer, W. Stadler
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引用次数: 7

摘要

摘要大多数男性转移性前列腺癌患者在接受雄激素剥夺治疗后,最终会发展为去势抵抗性疾病。在这篇综述中,我们研究了构成去势抵抗的分子机制,以及如何利用基于睾酮的治疗来利用这些过程。我们详细介绍了如何定期使用超生理剂量的睾丸激素,然后通过持续的化学阉割快速清除睾丸激素,也称为双极雄激素治疗,提供了一种特别有前途的治疗方法。我们调查了这种治疗方式的历史基础,详细介绍了最近的早期临床试验,这些试验已经证明了这种治疗的可行性和有效性,并描述了一项正在进行的临床试验,将这种治疗方式与目前公认的治疗标准恩杂鲁胺进行比较,以治疗去势抵抗性前列腺癌。最后,我们探讨了这种治疗方式将如何在未来继续完善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role of Testosterone in the Treatment of Castration-Resistant Prostate Cancer
AbstractMost men with metastatic prostate cancer who are treated with androgen deprivation therapy will eventually develop castration-resistant disease. In this review, we examine the molecular mechanisms that constitute castration resistance and how these processes may be exploited using testosterone-based therapies. We detail how the utilization of superphysiologic doses of testosterone at regular intervals, followed by a rapid clearance of testosterone through continued chemical castration, also known as bipolar androgen therapy, offers an especially promising therapeutic approach. We investigate the historical basis for this modality, detail recent early-phase clinical trials that have demonstrated the feasibility and efficacy of this treatment, and describe an ongoing clinical trial comparing this modality to a currently accepted standard of care, enzalutamide, for castration-resistant prostate cancer. Finally, we explore how this treatment modality will continue to be refined in the future.
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