Denosumab as treatment of central giant cell granuloma of the jaws. a scoping review.

Autor: Latorre CG; Faculty of Dentistry, Universidad Andres Bello, Viña del Mar, Chile., Atalah CN; Faculty of Dentistry, Universidad Andres Bello, Viña del Mar, Chile., Marshall Baburizza M; Faculty of Dentistry, Universidad Andres Bello, Viña del Mar, Chile. maureen.marshall@unab.cl.; Oral Pathology and Oral Medicine Unit, Faculty of Dentistry, Universidad Andres Bello, Quillota 980, Viña del Mar, Chile. maureen.marshall@unab.cl.
Jazyk: angličtina
Zdroj: Oral and maxillofacial surgery [Oral Maxillofac Surg] 2024 Sep; Vol. 28 (3), pp. 1029-1045. Date of Electronic Publication: 2024 Mar 28.
DOI: 10.1007/s10006-024-01245-y
Abstrakt: Denosumab has been considered a treatment option for Central Giant Cell Granuloma (CGCG) a benign locally aggressive osteolytic lesion of the jaws. This study aimed to perform a scoping review of CGCG treated with Denosumab. The research question was: What is Denosumab's effectiveness in treating CGCG of the jaws? Studies that used Denosumab as a treatment for CGCGs in the jaws were selected following PRISMA-ScR guidelines, using Pubmed/Medline, Scopus, and Springer Link databases, among others. Demographics, clinical information, dosing, efficacy, adverse drug reactions (ADRs), and imaging tests used to assess the evolution of the lesions were extracted. Twenty-one studies were selected. Sixty patients with a mean age of 23.2 years were treated with Denosumab, 42% with 120 mg subcutaneously monthly, additional doses on days 1, 8, and 15 for month 1 in adults. In children, dosing was adjusted by weight to 60 or 70 mg. To avoid ADRs 500 mg of calcium and 400 IU of vitamin D orally were used. Initial effective response was reported after 1-3 months, with recurrence of 19.6% and ADRs in 74% of cases. Denosumab is effective for CGCG with monthly subcutaneous doses of 120 mg, 60 or 70 mg in patients < 45 or 50 kg for ≥ 12 months with calcium and vitamin D supplementation until remission changes are observed. Extensive or refractory lesions were the main indications. Common ADRs were hypo and hypercalcemia. Further studies are needed to define dose and supplementation protocols to avoid ADRs during and after therapy.
(© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
Databáze: MEDLINE
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