Treatment Challenges When Stopping Denosumab.


Journal

Irish medical journal
ISSN: 0332-3102
Titre abrégé: Ir Med J
Pays: Ireland
ID NLM: 0430275

Informations de publication

Date de publication:
16 03 2022
Historique:
entrez: 9 5 2022
pubmed: 10 5 2022
medline: 12 5 2022
Statut: epublish

Résumé

Introduction Denosumab is commonly used to treat osteoporosis. However, discontinuation results in rebound bone loss and increased vertebral fracture risk. We report a clinical case series, illustrating the dilemma in deciding the best treatment should denosumab be stopped. Cases In eight patients aged 56-89 years, zolendronic acid after stopping denosumab resulted in BTM rises and BMD decline.  In a 68-year-old, two years of oral bisphosphonate after three years of denosumab resulted in elevated bone turnover markers (BTM) and decline in bone mineral density (BMD), necessitating a switch to zoledronic acid.  In a 79-year-old, two annual doses of zolendronic acid after three years of denosumab failed to suppress high BTM, with BMD dropping and denosumab being restarted.  In a 60-year-old, on stopping denosumab after 10 years of oral bisphosphonate, BMD remained stable despite no further therapy. Conclusion Drug holidays are not an option with denosumab, with a risk of bone loss even on transitioning to bisphosphonates. Risk is greater with longer duration of treatment6 and may be mitigated by prior bisphosphonate use. Standard dose zoledronic acid does not prevent bone loss in a significant proportion of patients. BTM may help in monitoring treatment and need for further bisphosphonates.

Identifiants

pubmed: 35532944

Substances chimiques

Bone Density Conservation Agents 0
Diphosphonates 0
Denosumab 4EQZ6YO2HI
Zoledronic Acid 6XC1PAD3KF

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

567

Commentaires et corrections

Type : CommentIn

Déclaration de conflit d'intérêts

The authors confirm that they have no conflicts of interest to declare.

Auteurs

A McDonough (A)

Bone Health and Osteoporosis Unit, Mercer's Institute for Successful Ageing, St. James's Hospital.

K Malomo (K)

Bone Health and Osteoporosis Unit, Mercer's Institute for Successful Ageing, St. James's Hospital.

F Brennan (F)

Bone Health and Osteoporosis Unit, Mercer's Institute for Successful Ageing, St. James's Hospital.

N Fallon (N)

Bone Health and Osteoporosis Unit, Mercer's Institute for Successful Ageing, St. James's Hospital.

G Steen (G)

Bone Health and Osteoporosis Unit, Mercer's Institute for Successful Ageing, St. James's Hospital.

N Maher (N)

Bone Health and Osteoporosis Unit, Mercer's Institute for Successful Ageing, St. James's Hospital.

C O'Carroll (C)

Bone Health and Osteoporosis Unit, Mercer's Institute for Successful Ageing, St. James's Hospital.

J B Walsh (JB)

Bone Health and Osteoporosis Unit, Mercer's Institute for Successful Ageing, St. James's Hospital.

R Lannon (R)

Bone Health and Osteoporosis Unit, Mercer's Institute for Successful Ageing, St. James's Hospital.

K McCarroll (K)

Bone Health and Osteoporosis Unit, Mercer's Institute for Successful Ageing, St. James's Hospital.

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Classifications MeSH