Risk of Osteonecrosis of the Jaw Under Denosumab Compared to Bisphosphonates in Patients With Osteoporosis.


Journal

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
ISSN: 1523-4681
Titre abrégé: J Bone Miner Res
Pays: United States
ID NLM: 8610640

Informations de publication

Date de publication:
02 2022
Historique:
revised: 05 11 2021
received: 18 08 2021
accepted: 09 11 2021
pubmed: 18 11 2021
medline: 15 3 2022
entrez: 17 11 2021
Statut: ppublish

Résumé

Osteonecrosis of the jaw (ONJ) is a rare but serious adverse event associated with antiresorptive treatment. There is little evidence regarding the incidence of ONJ among patients with osteoporosis who are treated with denosumab versus bisphosphonates (BPs). The aim of this study was to determine the risk of ONJ in a real-world population. Subjects who underwent at least one dual-energy X-ray absorptiometry (DXA) examination were included in the osteoporosis register of the Swiss Society of Rheumatology between January 1, 2015, and September 30, 2019. Statistical analyses included incidence rates, rate ratios, and hazard ratios for ONJ, considering sequential therapies and drug holidays as covariates. Among 9956 registered patients, 3068 (89% female, median age 69 years [63 to 76]) were treated with BPs or denosumab for a cumulative duration of 11,101 and 4236 patient-years, respectively. Seventeen cases of ONJ were identified: 12 in patients receiving denosumab at the time of ONJ diagnosis and 5 in patients receiving oral or intravenous BP therapy. The diagnosis of ONJ was confirmed by independent and blinded maxillofacial surgeons, using the American Association of Oral and Maxillofacial Surgeons case definition of ONJ. The incidence of ONJ per 10,000 observed patient-years was 28.3 in patients receiving denosumab and 4.5 in patients with BP-associated ONJ, yielding a rate ratio of 6.3 (95% confidence interval [CI] 2.1 to 22.8), p < 0.001. Nine of 12 patients who developed ONJ during denosumab treatment had been pretreated with BPs, but none of the 5 patients with BP-related ONJ had previously received denosumab. The risk of ONJ was higher in patients receiving denosumab therapy compared with BPs (hazard ratio 3.49, 95% CI 1.16 to 10.47, p = 0.026). Previous BP therapy before switching to denosumab may be an additional risk factor for ONJ development. © 2021 American Society for Bone and Mineral Research (ASBMR).

Identifiants

pubmed: 34787342
doi: 10.1002/jbmr.4472
doi:

Substances chimiques

Bone Density Conservation Agents 0
Diphosphonates 0
Denosumab 4EQZ6YO2HI

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

340-348

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2021 American Society for Bone and Mineral Research (ASBMR).

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Auteurs

Judith Everts-Graber (J)

OsteoRheuma Bern, Bern, Switzerland.
Department of Rheumatology and Immunology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Daniel Lehmann (D)

Faculty of Medicine, University of Bern, Bern, Switzerland.

John-Patrik Burkard (JP)

Department of Cranio-Maxillofacial Surgery, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Benoît Schaller (B)

Department of Cranio-Maxillofacial Surgery, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Brigitta Gahl (B)

Clinical Trial Unit, University of Bern, Bern, Switzerland.

HansJörg Häuselmann (H)

Zentrum für Rheuma- und Knochenerkrankungen, Zürich, Switzerland.

Ueli Studer (U)

OsteoRheuma Bern, Bern, Switzerland.

Hans-Rudolf Ziswiler (HR)

OsteoRheuma Bern, Bern, Switzerland.

Stephan Reichenbach (S)

Department of Rheumatology and Immunology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Institute for Social and Preventive Medicine, University of Bern, Bern, Switzerland.

Thomas Lehmann (T)

OsteoRheuma Bern, Bern, Switzerland.

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