French recommendations for osteoporosis prevention and treatment in patients with prostate cancer treated by androgen deprivation.

Abstract

Androgen-deprivation therapy (ADT) in patients with prostate cancer can be achieved surgically or chemically, notably by prescribing LHRH analogs. Major bone loss occurs rapidly in both cases, due to the decrease in testosterone levels, and can increase the fracture risk. The objective of developing these recommendations was to achieve a practical consensus among various scientific societies, based on a literature review, about osteoporosis prevention and treatment in patients on ADT. The following scientific societies contributed to the work: Société française de rhumatologie (SFR), Groupe de recherche et d'information sur les ostéoporoses (GRIO), Groupe européen d'études des métastases osseuses (GEMO), Association francophone pour les soins de support (AFSOS), Association française d'urologie (AFU), Société française de radiothérapie oncologique (SFRO). Medication prescription and reimbursement modalities in France were taken into account. The recommendations state that a fracture-risk evaluation and interventions targeting risk factors for fractures should be provided to all patients on ADT. Those patients with a history of severe osteoporotic fracture and/or a T-score < -2.5 should receive osteoporosis therapy. Patients whose T-score is between -1.5 and -2.5 should be treated if they exhibit at least two other risk factors among the following: age ≥ 75 years, history of non-severe fracture after 50 years of age, body mass index < 19 kg/m2, at least three comorbidities (e.g., cardiovascular disease, depression, Parkinson's disease, and dementia), current glucocorticoid therapy, and repeated falls. When the decision is difficult, FRAX® score determination and an assessment by a bone disease specialist may be helpful. When osteoporosis therapy is not indicated, general measures should be applied, and bone mineral density measured again after 12-24 months. The anti-tumor effects of bisphosphonates and denosumab fall outside the scope of these recommendations.

• Authors: Karine Briot, Julien Paccou, Philippe Beuzeboc, Jacques Bonneterre, Béatrice Bouvard, Cyrille B Confavreux, Catherine Cormier, Bernard Cortet, Jean-Michel Hannoun-Lévi, Christophe Hennequin, Rose-Marie Javier, Eric Lespessailles, Didier Mayeur, Pierre Mongiat Artus, Marie-Hélène Vieillard, Françoise Debiais
• Journal: Joint bone spine (Joint Bone Spine) Vol. 86 Issue 1 Pg. 21-28 (01 2019) ISSN: 1778-7254 [Electronic] France
• PMID: 30287350 (Publication Type: Journal Article, Review)
• Copyright: Copyright © 2018. Published by Elsevier Masson SAS.

Chemical References

• Androgen Antagonists
• Diphosphonates
• Gonadotropin-Releasing Hormone

Topics

• Androgen Antagonists (adverse effects, therapeutic use)
• Bone Density (drug effects, physiology)
• Bone Resorption (chemically induced, etiology)
• Diphosphonates (therapeutic use)
• France
• Gonadotropin-Releasing Hormone (analogs & derivatives, antagonists & inhibitors, therapeutic use)
• Humans
• Male
• Orchiectomy (adverse effects)
• Osteoporosis (chemically induced, etiology, prevention & control, therapy)
• Osteoporotic Fractures (chemically induced, etiology, prevention & control, therapy)
• Prostatectomy
• Prostatic Neoplasms (drug therapy, surgery, therapy)
• Risk Assessment
• Risk Factors