# Adherence to denosumab therapy and fracture risk associated with drug withdrawal: a retrospective study

**Authors:** Hande Özdemir, Nur Kakilli, Filiz Tuna, Buket Yılmaz Bülbül, Mehmet Çelik, Selçuk Korkmaz, Derya Demirbağ Kabayel

PMC · DOI: 10.3325/cmj.2025.66.334 · Croatian Medical Journal · 2025-10-01

## TL;DR

This study examines how stopping denosumab treatment affects fracture risk and finds that fractures may occur due to osteoporosis progression, not just treatment discontinuation.

## Contribution

The study provides new insights into fracture risk after denosumab discontinuation and treatment adherence factors in osteoporosis patients.

## Key findings

- Adherent and non-adherent patients had similar fracture risks after denosumab discontinuation.
- Fractures may result from osteoporosis progression rather than a rebound effect from drug withdrawal.
- Unscheduled treatment discontinuation should be avoided to manage osteoporosis effectively.

## Abstract

To assess the prevalence of fragility fractures after denosumab discontinuation and to identify the factors affecting treatment adherence.

We retrospectively reviewed the medical records of 3876 osteoporosis patients who were treated with denosumab at Trakya University Osteoporosis Clinic between 2015 and 2021. A total of 210 patients who received at least two regular doses of denosumab were eligible for inclusion. Patients were categorized as denosumab-adherent and denosumab-non-adherent. Adherence was defined as receiving the six-month scheduled dose with a maximum delay of up to eight weeks.

Overall, 124 (59.05%) patients were denosumab-adherent and 86 patients (40.95%) were denosumab-non-adherent. New fragility fractures were identified in 32 patients: 17 in the denosumab-adherent group and 15 in the denosumab-non-adherent group. The groups did not significantly differ in the risk or types of new fractures, irrespective of patients’ fracture history.

Our findings suggest that some fractures after denosumab discontinuation may stem from the natural progression of osteoporosis rather than from the rebound effect. Still, unscheduled treatment discontinuation should be prevented.

## Linked entities

- **Diseases:** osteoporosis (MONDO:0005298)

## Full-text entities

- **Diseases:** Osteoporosis (MESH:D010024), fragility fractures (MESH:D005600), fracture (MESH:D050723)
- **Chemicals:** denosumab (MESH:D000069448)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12623255/full.md

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Source: https://tomesphere.com/paper/PMC12623255