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Dosing interval adjustment of denosumab for the treatment of giant cell tumor of the sphenoid bone: A case report
BACKGROUND: In the treatment of giant cell tumor of bone (GCTB), the efficacy and safety of denosumab, a receptor activator nuclear factor κ-B ligand inhibitor, has previously been demonstrated, especially for unresectable tumors. One of the current issues in denosumab treatment for unresectable GCT...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Scientific Scholar
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771493/ https://www.ncbi.nlm.nih.gov/pubmed/33408904 http://dx.doi.org/10.25259/SNI_439_2020 |
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author | Tanikawa, Motoki Yamada, Hiroshi Sakata, Tomohiro Mase, Mitsuhito |
author_facet | Tanikawa, Motoki Yamada, Hiroshi Sakata, Tomohiro Mase, Mitsuhito |
author_sort | Tanikawa, Motoki |
collection | PubMed |
description | BACKGROUND: In the treatment of giant cell tumor of bone (GCTB), the efficacy and safety of denosumab, a receptor activator nuclear factor κ-B ligand inhibitor, has previously been demonstrated, especially for unresectable tumors. One of the current issues in denosumab treatment for unresectable GCTB is whether it can be discontinued, or whether the dosage or the dosing interval can safely be adjusted, if discontinuation is not possible, to avoid the occurrence of side effects. CASE DESCRIPTION: A 15-year-old boy with diplopia was referred to our hospital after a space-occupying lesion in the sphenoid bone was found on head CT. Partial removal of the tumor was performed through an endoscopic endonasal approach, and pathological diagnosis was confirmed as GCTB. Thereafter, the patient received 120 mg subcutaneous injections of denosumab every 28 days for the first 2 years. Since bone formation was induced and sustained along with tumor reduction, the dosing interval was gradually extended, with 4 monthly dosing for the next 1 year, followed by 6 monthly dosing for the succeeding 2 years. With the extension of the dosing interval, the ossified tumor has regrown slightly, but within an acceptable range. CONCLUSION: Discontinuation of denosumab treatment for unresectable GCTB was not thought to be possible for the current case due to the nature of the drug, as reported in the literature. Extending the dosing interval up to 6 monthly, as could be done safely in the current case, can be considered a useful and appropriate measure. |
format | Online Article Text |
id | pubmed-7771493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-77714932021-01-05 Dosing interval adjustment of denosumab for the treatment of giant cell tumor of the sphenoid bone: A case report Tanikawa, Motoki Yamada, Hiroshi Sakata, Tomohiro Mase, Mitsuhito Surg Neurol Int Case Report BACKGROUND: In the treatment of giant cell tumor of bone (GCTB), the efficacy and safety of denosumab, a receptor activator nuclear factor κ-B ligand inhibitor, has previously been demonstrated, especially for unresectable tumors. One of the current issues in denosumab treatment for unresectable GCTB is whether it can be discontinued, or whether the dosage or the dosing interval can safely be adjusted, if discontinuation is not possible, to avoid the occurrence of side effects. CASE DESCRIPTION: A 15-year-old boy with diplopia was referred to our hospital after a space-occupying lesion in the sphenoid bone was found on head CT. Partial removal of the tumor was performed through an endoscopic endonasal approach, and pathological diagnosis was confirmed as GCTB. Thereafter, the patient received 120 mg subcutaneous injections of denosumab every 28 days for the first 2 years. Since bone formation was induced and sustained along with tumor reduction, the dosing interval was gradually extended, with 4 monthly dosing for the next 1 year, followed by 6 monthly dosing for the succeeding 2 years. With the extension of the dosing interval, the ossified tumor has regrown slightly, but within an acceptable range. CONCLUSION: Discontinuation of denosumab treatment for unresectable GCTB was not thought to be possible for the current case due to the nature of the drug, as reported in the literature. Extending the dosing interval up to 6 monthly, as could be done safely in the current case, can be considered a useful and appropriate measure. Scientific Scholar 2020-11-06 /pmc/articles/PMC7771493/ /pubmed/33408904 http://dx.doi.org/10.25259/SNI_439_2020 Text en Copyright: © 2020 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Tanikawa, Motoki Yamada, Hiroshi Sakata, Tomohiro Mase, Mitsuhito Dosing interval adjustment of denosumab for the treatment of giant cell tumor of the sphenoid bone: A case report |
title | Dosing interval adjustment of denosumab for the treatment of giant cell tumor of the sphenoid bone: A case report |
title_full | Dosing interval adjustment of denosumab for the treatment of giant cell tumor of the sphenoid bone: A case report |
title_fullStr | Dosing interval adjustment of denosumab for the treatment of giant cell tumor of the sphenoid bone: A case report |
title_full_unstemmed | Dosing interval adjustment of denosumab for the treatment of giant cell tumor of the sphenoid bone: A case report |
title_short | Dosing interval adjustment of denosumab for the treatment of giant cell tumor of the sphenoid bone: A case report |
title_sort | dosing interval adjustment of denosumab for the treatment of giant cell tumor of the sphenoid bone: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771493/ https://www.ncbi.nlm.nih.gov/pubmed/33408904 http://dx.doi.org/10.25259/SNI_439_2020 |
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