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Erschienen in:

07.06.2019 | Original Article

Fracture risk following intermission of osteoporosis therapy

verfasst von: E.M. Dennison, C. Cooper, J.A. Kanis, O. Bruyère, S. Silverman, E. McCloskey, B. Abrahamsen, D. Prieto-Alhambra, S. Ferrari, On behalf of the IOF Epidemiology/Quality of Life Working Group

Erschienen in: Osteoporosis International | Ausgabe 9/2019

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Abstract

Summary

Given the widespread practice of recommending drug holidays, we reviewed the impact of medication discontinuation of two common anti-osteoporosis therapies (bisphosphonates and denosumab). Trial evidence suggests the risk of new clinical fractures, and vertebral fracture increases when osteoporosis treatment with bisphosphonates or denosumab is stopped.

Introduction

The aim of this paper was to review the available literature to assess what evidence exists to inform clinical decision-making with regard to drug holidays following treatment with bisphosphonates (BiP) or denosumab.

Methods

Systematic review.

Results

Differing pharmacokinetics lead to varying outcomes on stopping therapy. Prospective and retrospective analyses report that the risk of new clinical fractures was 20–40% higher in subjects who stopped BiP treatment, and vertebral fracture risk was approximately doubled. Rapid bone loss has been well described following denosumab discontinuation with an incidence of multiple vertebral fractures around 5%. Studies have not identified risk factors for fracture after stopping treatment other than those that provide an indication for treatment (e.g. prior fracture and low BMD). Studies that considered long-term continuation did not identify increased fracture risk, and reported only very low rates of adverse skeletal events such as atypical femoral fracture.

Conclusions

The view that patients on long-term treatment with bisphosphonates or denosumab should always be offered a drug holiday is not supported by the existing evidence. Different pharmacokinetic properties for different therapies require different strategies to manage drug intermission. In contrast, long-term treatment with anti-resorptives is not associated with increased risk of fragility fractures and skeletal adverse events remain rare.

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Titel: Fracture risk following intermission of osteoporosis therapy
verfasst von: E.M. Dennison
C. Cooper
J.A. Kanis
O. Bruyère
S. Silverman
E. McCloskey
B. Abrahamsen
D. Prieto-Alhambra
S. Ferrari
On behalf of the IOF Epidemiology/Quality of Life Working Group
Publikationsdatum: 07.06.2019
Verlag: Springer London
Erschienen in: Osteoporosis International / Ausgabe 9/2019
Print ISSN: 0937-941X
Elektronische ISSN: 1433-2965
DOI: https://doi.org/10.1007/s00198-019-05002-w

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Fracture risk following intermission of osteoporosis therapy

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Abstract

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