Long-Term Follow-Up of Denosumab Discontinuers with Multiple Vertebral Fractures in the Real-World: A Case Series.


Journal

Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
ISSN: 1439-4286
Titre abrégé: Horm Metab Res
Pays: Germany
ID NLM: 0177722

Informations de publication

Date de publication:
Mar 2021
Historique:
pubmed: 16 2 2021
medline: 27 10 2021
entrez: 15 2 2021
Statut: ppublish

Résumé

Denosumab discontinuation is associated with rapid reversal of bone turnover suppression and with a considerable increase in fracture risk, including a risk for multiple vertebral fractures (MVF). Long-term follow-up of patients who sustained MVF after denosumab discontinuation has not been reported. This case-series was aimed to provide a long-term follow-up on the management and outcome of denosumab discontinuers who initially presented with multiple vertebral fractures. Denosumab discontinuers were identified from a computerized database of a large healthcare provider. Baseline and follow-up clinical, laboratory, and imaging data were obtained from the computerized database and electronic medical records. The post-denosumab discontinuers MVF patients consisted of 12 women aged 71±12. Osteoporotic fractures were prevalent before denosumab discontinuation in 6 of the patients. The majority received bisphosphonates before denosumab. MVF occurred 134±76 days after denosumab discontinuation. The patients were followed for a median of 36.5 (IQR 28.2, 42.5) months after MVF. Two patients passed-away. Two patients suffered recurrent vertebral fractures. Following MVF, patients were treated inconsistently with denosumab, teriparatide, oral, and intravenous bisphosphonates, in various sequences. Two patients underwent vertebroplasty/kyphoplasty. This long-term follow-up of real-world patients with MVF following denosumab discontinuation reveals that management is inconsistent, and recurrent fractures are not uncommon. It calls for clear management guidelines for patients with MVF after denosumab discontinuation and for special attention to this high-risk group.

Identifiants

pubmed: 33588445
doi: 10.1055/a-1368-4218
doi:

Substances chimiques

Bone Density Conservation Agents 0
Denosumab 4EQZ6YO2HI

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

185-190

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

The core study 1 was investigator-initiated and was supported by Amgen. The current analysis was not sponsored. Dr. Tripto-Shkolnik reports personal fees from Amgen, personal fees from Eli Lilly, outside the submitted work. Prof. Yair Liel, Naama Yekutiel and Dr. Inbal Goldshtein, have nothing to disclose.

Auteurs

Liana Tripto-Shkolnik (L)

Division of Endocrinology, Diabetes and Metabolism, Chaim Sheba Medical Center at Tel Hashomer, Ramat Gan, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Yair Liel (Y)

Ben-Gurion University of the Negev, Beer-Sheva, Israel.

Naama Yekutiel (N)

Maccabitech Institute of Research and Innovation, Maccabi Healthcare Services, Tel Aviv, Israel.

Inbal Goldshtein (I)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Maccabitech Institute of Research and Innovation, Maccabi Healthcare Services, Tel Aviv, Israel.

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Classifications MeSH