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Malignancy in giant cell tumor of bone: analysis of an open-label phase 2 study of denosumab
BACKGROUND: Giant cell tumor of bone (GCTB) is a rare osteoclastogenic stromal tumor. GCTB can rarely undergo malignant transformation. This post hoc analysis evaluated and classified malignancies in patients with GCTB who received denosumab. METHODS: This analysis was conducted on patients with pat...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824947/ https://www.ncbi.nlm.nih.gov/pubmed/33482769 http://dx.doi.org/10.1186/s12885-020-07739-8 |
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author | Palmerini, Emanuela Seeger, Leanne L. Gambarotti, Marco Righi, Alberto Reichardt, Peter Bukata, Susan Blay, Jean-Yves Dai, Tian Jandial, Danielle Picci, Piero |
author_facet | Palmerini, Emanuela Seeger, Leanne L. Gambarotti, Marco Righi, Alberto Reichardt, Peter Bukata, Susan Blay, Jean-Yves Dai, Tian Jandial, Danielle Picci, Piero |
author_sort | Palmerini, Emanuela |
collection | PubMed |
description | BACKGROUND: Giant cell tumor of bone (GCTB) is a rare osteoclastogenic stromal tumor. GCTB can rarely undergo malignant transformation. This post hoc analysis evaluated and classified malignancies in patients with GCTB who received denosumab. METHODS: This analysis was conducted on patients with pathologically confirmed GCTB and measurable active disease treated with denosumab 120 mg subcutaneously once every 4 weeks, with loading doses on study days 8 and 15, as part of a phase 2, open-label, multicenter study. We identified potential cases of malignancy related to GCTB through an independent multidisciplinary review or medical history, associated imaging or histopathologic reports, and disease course. The findings were summarized and no statistical analysis was performed. RESULTS: Twenty of five hundred twenty-six patients (3.8%) who received at least one dose of denosumab were misdiagnosed with GCTB that was later discovered to be malignancies: five primary malignant GCTB, five secondary malignant GCTB, four sarcomatous transformations, and six patients with other malignancies (giant cell-rich osteosarcoma, undifferentiated pleomorphic sarcoma, spindle cell sarcoma, osteogenic sarcoma, phosphaturic mesenchymal tumor of mixed connective tissue type, and fibrosarcoma/malignant fibrous histiocytoma). Many malignancies were present before denosumab was initiated (8 definitive cases, 7 likely cases), excluding potential involvement of denosumab in these cases. Signs associated with potential misdiagnoses of GCTB included poor mineralization with denosumab treatment, rapid relapse in pain, or a failure of the typical dramatic improvement in pain normally observed with denosumab. CONCLUSIONS: Although rare, GCTB can undergo malignant transformation, and rates in this study were consistent with previous reports. Signs of poor mineralization or lack of response to denosumab treatment may warrant close monitoring. TRIAL REGISTRATION: clinicaltrials.gov, (NCT00680992). Registered May 20, 2008. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-020-07739-8. |
format | Online Article Text |
id | pubmed-7824947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78249472021-01-25 Malignancy in giant cell tumor of bone: analysis of an open-label phase 2 study of denosumab Palmerini, Emanuela Seeger, Leanne L. Gambarotti, Marco Righi, Alberto Reichardt, Peter Bukata, Susan Blay, Jean-Yves Dai, Tian Jandial, Danielle Picci, Piero BMC Cancer Research Article BACKGROUND: Giant cell tumor of bone (GCTB) is a rare osteoclastogenic stromal tumor. GCTB can rarely undergo malignant transformation. This post hoc analysis evaluated and classified malignancies in patients with GCTB who received denosumab. METHODS: This analysis was conducted on patients with pathologically confirmed GCTB and measurable active disease treated with denosumab 120 mg subcutaneously once every 4 weeks, with loading doses on study days 8 and 15, as part of a phase 2, open-label, multicenter study. We identified potential cases of malignancy related to GCTB through an independent multidisciplinary review or medical history, associated imaging or histopathologic reports, and disease course. The findings were summarized and no statistical analysis was performed. RESULTS: Twenty of five hundred twenty-six patients (3.8%) who received at least one dose of denosumab were misdiagnosed with GCTB that was later discovered to be malignancies: five primary malignant GCTB, five secondary malignant GCTB, four sarcomatous transformations, and six patients with other malignancies (giant cell-rich osteosarcoma, undifferentiated pleomorphic sarcoma, spindle cell sarcoma, osteogenic sarcoma, phosphaturic mesenchymal tumor of mixed connective tissue type, and fibrosarcoma/malignant fibrous histiocytoma). Many malignancies were present before denosumab was initiated (8 definitive cases, 7 likely cases), excluding potential involvement of denosumab in these cases. Signs associated with potential misdiagnoses of GCTB included poor mineralization with denosumab treatment, rapid relapse in pain, or a failure of the typical dramatic improvement in pain normally observed with denosumab. CONCLUSIONS: Although rare, GCTB can undergo malignant transformation, and rates in this study were consistent with previous reports. Signs of poor mineralization or lack of response to denosumab treatment may warrant close monitoring. TRIAL REGISTRATION: clinicaltrials.gov, (NCT00680992). Registered May 20, 2008. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-020-07739-8. BioMed Central 2021-01-22 /pmc/articles/PMC7824947/ /pubmed/33482769 http://dx.doi.org/10.1186/s12885-020-07739-8 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Palmerini, Emanuela Seeger, Leanne L. Gambarotti, Marco Righi, Alberto Reichardt, Peter Bukata, Susan Blay, Jean-Yves Dai, Tian Jandial, Danielle Picci, Piero Malignancy in giant cell tumor of bone: analysis of an open-label phase 2 study of denosumab |
title | Malignancy in giant cell tumor of bone: analysis of an open-label phase 2 study of denosumab |
title_full | Malignancy in giant cell tumor of bone: analysis of an open-label phase 2 study of denosumab |
title_fullStr | Malignancy in giant cell tumor of bone: analysis of an open-label phase 2 study of denosumab |
title_full_unstemmed | Malignancy in giant cell tumor of bone: analysis of an open-label phase 2 study of denosumab |
title_short | Malignancy in giant cell tumor of bone: analysis of an open-label phase 2 study of denosumab |
title_sort | malignancy in giant cell tumor of bone: analysis of an open-label phase 2 study of denosumab |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824947/ https://www.ncbi.nlm.nih.gov/pubmed/33482769 http://dx.doi.org/10.1186/s12885-020-07739-8 |
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