Effects of Medical Treatment of Prostate Cancer on Bone Health

Trends Endocrinol Metab. 2021 Mar;32(3):135-158. doi: 10.1016/j.tem.2020.12.004. Epub 2021 Jan 26.

Abstract

Medical treatment of prostate cancer (PC) is multidisciplinary, resulting in prolonged survival. Androgen-deprivation therapy (ADT) can have negative effects on skeletal metabolism, particularly if combined with glucocorticoids. We discuss the pathophysiology and effects of ADT and glucocorticoids on skeletal endpoints, as well as the awareness and management of bone fragility. Coadministration of glucocorticoids is necessary with abiraterone because this causes a novel acquired form of 17-hydroxylase deficiency and synergistically increases the risk of fracture by affecting bone quality. Bone antiresorptive agents [selective estrogen receptor modulators (SERMS), bisphosphonates, and denosumab] increase bone mineral density (BMD) and in some instances reduce fracture risk in PC patients on ADT. Awareness and management of bone health in PC can be improved by integrating endocrinologists into the multidisciplinary PC team.

Keywords: androgen deprivation; bone mineral density; fractures; glucocorticoids; prostate cancer.

Publication types

  • Review

MeSH terms

  • Androgen Antagonists
  • Animals
  • Bone Density / physiology*
  • Glucocorticoids / metabolism
  • Humans
  • Male
  • Prostatic Neoplasms / physiopathology*

Substances

  • Androgen Antagonists
  • Glucocorticoids