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Safety and efficacy of denosumab in the treatment of pulmonary metastatic giant cell tumor of bone
BACKGROUND: Giant cell tumor (GCT) of bone is an intermittent and locally aggressive tumor with increasing pulmonary metastatic potential. In this study, we evaluated the interim clinical outcome of denosumab in patients with pulmonary metastatic GCT. MATERIALS AND METHODS: We retrospectively review...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038885/ https://www.ncbi.nlm.nih.gov/pubmed/30013396 http://dx.doi.org/10.2147/CMAR.S161871 |
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author | Luo, Yi Tang, Fan Wang, Yitian Zhou, Yong Min, Li Zhang, Wenli Shi, Rui Duan, Hong Tu, Chongqi |
author_facet | Luo, Yi Tang, Fan Wang, Yitian Zhou, Yong Min, Li Zhang, Wenli Shi, Rui Duan, Hong Tu, Chongqi |
author_sort | Luo, Yi |
collection | PubMed |
description | BACKGROUND: Giant cell tumor (GCT) of bone is an intermittent and locally aggressive tumor with increasing pulmonary metastatic potential. In this study, we evaluated the interim clinical outcome of denosumab in patients with pulmonary metastatic GCT. MATERIALS AND METHODS: We retrospectively reviewed seven patients with pulmonary metastatic GCT who received denosumab treatment after local tumor surgery during January 2014 and July 2016. Denosumab treatment for all patients lasted for at least 12 months. Serial chest computerized tomography scan was used to monitor the drug response and RECIST 1.1 standard was used to evaluate the therapeutic efficacy. RESULTS: All patients experienced chest pain relief in the first month of treatment. Three patients showed partial response. Four patients got stable disease after denosumab treatment. Adverse events included one patient with hypocalcemia and two patients with fever. No treatment-related deaths were reported. No patient with metastatic disease progression was found during an average of 28.6 months follow-up period. CONCLUSION: We presented a promising interim clinical outcome using denosumab to treat patients with pulmonary metastatic GCT. Denosumab might be considered as the first-line treatment for patients with inoperable metastatic pulmonary GCT. However, Phase II clinical study with larger number of patients and longer follow-up period is needed to detect the further efficacy and safety of this drug for lung metastatic GCT. |
format | Online Article Text |
id | pubmed-6038885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60388852018-07-16 Safety and efficacy of denosumab in the treatment of pulmonary metastatic giant cell tumor of bone Luo, Yi Tang, Fan Wang, Yitian Zhou, Yong Min, Li Zhang, Wenli Shi, Rui Duan, Hong Tu, Chongqi Cancer Manag Res Original Research BACKGROUND: Giant cell tumor (GCT) of bone is an intermittent and locally aggressive tumor with increasing pulmonary metastatic potential. In this study, we evaluated the interim clinical outcome of denosumab in patients with pulmonary metastatic GCT. MATERIALS AND METHODS: We retrospectively reviewed seven patients with pulmonary metastatic GCT who received denosumab treatment after local tumor surgery during January 2014 and July 2016. Denosumab treatment for all patients lasted for at least 12 months. Serial chest computerized tomography scan was used to monitor the drug response and RECIST 1.1 standard was used to evaluate the therapeutic efficacy. RESULTS: All patients experienced chest pain relief in the first month of treatment. Three patients showed partial response. Four patients got stable disease after denosumab treatment. Adverse events included one patient with hypocalcemia and two patients with fever. No treatment-related deaths were reported. No patient with metastatic disease progression was found during an average of 28.6 months follow-up period. CONCLUSION: We presented a promising interim clinical outcome using denosumab to treat patients with pulmonary metastatic GCT. Denosumab might be considered as the first-line treatment for patients with inoperable metastatic pulmonary GCT. However, Phase II clinical study with larger number of patients and longer follow-up period is needed to detect the further efficacy and safety of this drug for lung metastatic GCT. Dove Medical Press 2018-07-05 /pmc/articles/PMC6038885/ /pubmed/30013396 http://dx.doi.org/10.2147/CMAR.S161871 Text en © 2018 Luo et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Luo, Yi Tang, Fan Wang, Yitian Zhou, Yong Min, Li Zhang, Wenli Shi, Rui Duan, Hong Tu, Chongqi Safety and efficacy of denosumab in the treatment of pulmonary metastatic giant cell tumor of bone |
title | Safety and efficacy of denosumab in the treatment of pulmonary metastatic giant cell tumor of bone |
title_full | Safety and efficacy of denosumab in the treatment of pulmonary metastatic giant cell tumor of bone |
title_fullStr | Safety and efficacy of denosumab in the treatment of pulmonary metastatic giant cell tumor of bone |
title_full_unstemmed | Safety and efficacy of denosumab in the treatment of pulmonary metastatic giant cell tumor of bone |
title_short | Safety and efficacy of denosumab in the treatment of pulmonary metastatic giant cell tumor of bone |
title_sort | safety and efficacy of denosumab in the treatment of pulmonary metastatic giant cell tumor of bone |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038885/ https://www.ncbi.nlm.nih.gov/pubmed/30013396 http://dx.doi.org/10.2147/CMAR.S161871 |
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