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Objective tumor response to denosumab in patients with giant cell tumor of bone: a multicenter phase II trial
BACKGROUND: Giant cell tumor of bone (GCTB) is a rare primary bone tumor, characterized by osteoclast-like giant cells that express receptor activator of nuclear factor-kappa B (RANK), and stromal cells that express RANK ligand (RANKL), a key mediator of osteoclast activation. A RANKL-specific inhib...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576909/ https://www.ncbi.nlm.nih.gov/pubmed/26205395 http://dx.doi.org/10.1093/annonc/mdv307 |
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author | Ueda, T. Morioka, H. Nishida, Y. Kakunaga, S. Tsuchiya, H. Matsumoto, Y. Asami, Y. Inoue, T. Yoneda, T. |
author_facet | Ueda, T. Morioka, H. Nishida, Y. Kakunaga, S. Tsuchiya, H. Matsumoto, Y. Asami, Y. Inoue, T. Yoneda, T. |
author_sort | Ueda, T. |
collection | PubMed |
description | BACKGROUND: Giant cell tumor of bone (GCTB) is a rare primary bone tumor, characterized by osteoclast-like giant cells that express receptor activator of nuclear factor-kappa B (RANK), and stromal cells that express RANK ligand (RANKL), a key mediator of osteoclast activation. A RANKL-specific inhibitor, denosumab, was predicted to reduce osteolysis and control disease progression in patients with GCTB. PATIENTS AND METHODS: Seventeen patients with GCTB were enrolled. Patients were treated with denosumab at 120 mg every 4 weeks, with a loading dose of 120 mg on days 8 and 15. To evaluate efficacy, objective tumor response was evaluated prospectively by an independent imaging facility on the basis of prespecified criteria. RESULTS: The proportion of patients with an objective tumor response was 88% based on best response using any tumor response criteria. The proportion of patients with an objective tumor response using individual response criteria was 35% based on the modified Response Evaluation Criteria in Solid Tumors (RECIST) criteria, 82% based on the modified European Organization for Research and Treatment of Cancer (EORTC) criteria, and 71% based on inverse Choi criteria. The median time of study treatment was 13.1 months. CONCLUSION: The findings demonstrate that denosumab has robust clinical efficacy in the treatment of GCTB. |
format | Online Article Text |
id | pubmed-4576909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45769092015-09-25 Objective tumor response to denosumab in patients with giant cell tumor of bone: a multicenter phase II trial Ueda, T. Morioka, H. Nishida, Y. Kakunaga, S. Tsuchiya, H. Matsumoto, Y. Asami, Y. Inoue, T. Yoneda, T. Ann Oncol Original Articles BACKGROUND: Giant cell tumor of bone (GCTB) is a rare primary bone tumor, characterized by osteoclast-like giant cells that express receptor activator of nuclear factor-kappa B (RANK), and stromal cells that express RANK ligand (RANKL), a key mediator of osteoclast activation. A RANKL-specific inhibitor, denosumab, was predicted to reduce osteolysis and control disease progression in patients with GCTB. PATIENTS AND METHODS: Seventeen patients with GCTB were enrolled. Patients were treated with denosumab at 120 mg every 4 weeks, with a loading dose of 120 mg on days 8 and 15. To evaluate efficacy, objective tumor response was evaluated prospectively by an independent imaging facility on the basis of prespecified criteria. RESULTS: The proportion of patients with an objective tumor response was 88% based on best response using any tumor response criteria. The proportion of patients with an objective tumor response using individual response criteria was 35% based on the modified Response Evaluation Criteria in Solid Tumors (RECIST) criteria, 82% based on the modified European Organization for Research and Treatment of Cancer (EORTC) criteria, and 71% based on inverse Choi criteria. The median time of study treatment was 13.1 months. CONCLUSION: The findings demonstrate that denosumab has robust clinical efficacy in the treatment of GCTB. Oxford University Press 2015-10 2015-07-23 /pmc/articles/PMC4576909/ /pubmed/26205395 http://dx.doi.org/10.1093/annonc/mdv307 Text en © The Author 2015. Published by Oxford University Press on behalf of the European Society for Medical Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Articles Ueda, T. Morioka, H. Nishida, Y. Kakunaga, S. Tsuchiya, H. Matsumoto, Y. Asami, Y. Inoue, T. Yoneda, T. Objective tumor response to denosumab in patients with giant cell tumor of bone: a multicenter phase II trial |
title | Objective tumor response to denosumab in patients with giant cell tumor of bone: a multicenter phase II trial |
title_full | Objective tumor response to denosumab in patients with giant cell tumor of bone: a multicenter phase II trial |
title_fullStr | Objective tumor response to denosumab in patients with giant cell tumor of bone: a multicenter phase II trial |
title_full_unstemmed | Objective tumor response to denosumab in patients with giant cell tumor of bone: a multicenter phase II trial |
title_short | Objective tumor response to denosumab in patients with giant cell tumor of bone: a multicenter phase II trial |
title_sort | objective tumor response to denosumab in patients with giant cell tumor of bone: a multicenter phase ii trial |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576909/ https://www.ncbi.nlm.nih.gov/pubmed/26205395 http://dx.doi.org/10.1093/annonc/mdv307 |
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