Novel androgen receptor inhibitors for metastatic hormone-sensitive prostate cancer: Current application and future perspectives

Biomed Pharmacother. 2023 Dec:168:115806. doi: 10.1016/j.biopha.2023.115806. Epub 2023 Nov 6.

Abstract

Androgen receptor (AR) signaling is essential in prostate cancer treatment. For many years, androgen deprivation therapy (ADT) has been primarily applied to manage advanced prostate cancer. However, most individuals with metastatic hormone-sensitive prostate cancer (mHSPC) administered ADT alone are at risk of developing metastatic castration-resistant prostate cancer (mCRPC) in less than two years. New approaches employing novel AR inhibitors (ARi) as intensified upfront systemic treatment in mHSPC have recently demonstrated substantial benefits in delaying disease progression and prolonging overall survival. Administration of novel ARi has become the new standard of care in mHSPC. The new landscape simultaneously makes treatment choice more challenging. This review provides comprehensive data on molecular structure, pharmaceutical properties, and efficacy and safety profiles reported by pivotal clinical trials. We also discuss future directions with ongoing Phase III trials of novel ARi in mHSPC. Considering these biological and clinical insights, this review aimed to provide a comprehensive understanding of differences in the development and applications of novel ARi for mHSPC, which may be helpful in designing strategies for first-line treatment choices.

Keywords: Androgen deprivation therapy; Metastatic hormone-sensitive prostate cancer; Novel androgen receptor inhibitors; Treatment choice.

Publication types

  • Review

MeSH terms

  • Androgen Receptor Antagonists* / pharmacology
  • Androgen Receptor Antagonists* / therapeutic use
  • Hormones
  • Humans
  • Male
  • Prostatic Neoplasms* / drug therapy
  • Prostatic Neoplasms* / pathology
  • Prostatic Neoplasms, Castration-Resistant* / pathology
  • Receptors, Androgen
  • Treatment Outcome

Substances

  • Androgen Receptor Antagonists
  • Hormones
  • Receptors, Androgen