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Denosumab treatment of inoperable or locally advanced giant cell tumor of bone

Giant cell tumor of bone (GCTB) is an osteolytic, locally aggressive tumor that rarely metastasizes and typically occurs in the bones. At present, the primary treatment for GCTB is curettage with local adjuvants. Giant cells express receptor activator of nuclear factor-κB ligand (RANKL). Denosumab,...

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Autores principales: Borkowska, Aneta, Goryń, Tomasz, Pieńkowski, Andrzej, Wągrodzki, Michał, Jagiełło-Wieczorek, Ewelina, Rogala, Paweł, Szacht, Milena, Rutkowski, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5228072/
https://www.ncbi.nlm.nih.gov/pubmed/28101196
http://dx.doi.org/10.3892/ol.2016.5246
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author Borkowska, Aneta
Goryń, Tomasz
Pieńkowski, Andrzej
Wągrodzki, Michał
Jagiełło-Wieczorek, Ewelina
Rogala, Paweł
Szacht, Milena
Rutkowski, Piotr
author_facet Borkowska, Aneta
Goryń, Tomasz
Pieńkowski, Andrzej
Wągrodzki, Michał
Jagiełło-Wieczorek, Ewelina
Rogala, Paweł
Szacht, Milena
Rutkowski, Piotr
author_sort Borkowska, Aneta
collection PubMed
description Giant cell tumor of bone (GCTB) is an osteolytic, locally aggressive tumor that rarely metastasizes and typically occurs in the bones. At present, the primary treatment for GCTB is curettage with local adjuvants. Giant cells express receptor activator of nuclear factor-κB ligand (RANKL). Denosumab, a RANKL inhibitor appears to present an effective therapeutic option in advanced cases of GCTB. The aim of the present study was to confirm the efficacy of denosumab in large group of patients with locally advanced GCTB. A total of 35 patients with histologically confirmed GCTB that were treated with denosumab with no participation in clinical trials between May 2013 and September 2015 were included in the present study. Denosumab treatment was administered until complete tumor resection was feasible or tumor progression or unacceptable toxicity had occurred. The mean denosumab treatment duration was 7.4 months. A total of 17 patients received surgery following denosumab treatment: 11 patients underwent wide en bloc resection with prosthesis implantation in 10 cases and 6 patients were treated with intralesional curettage. Tumor progression was observed in 2 patients that underwent intralesional curettage without prosthesis implantation. In addition, tumor progression was observed during denosumab treatment in 2 patients that had previously undergone radiotherapy. The overall 1-year progression-free survival rate was 92.8%. Thus, for patients with advanced, unresectable, progressive or symptomatic pretreated GCTB, denosumab provides a therapeutic option not previously available, which has become the standard therapy in multidisciplinary management of GCTB.
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spelling pubmed-52280722017-01-18 Denosumab treatment of inoperable or locally advanced giant cell tumor of bone Borkowska, Aneta Goryń, Tomasz Pieńkowski, Andrzej Wągrodzki, Michał Jagiełło-Wieczorek, Ewelina Rogala, Paweł Szacht, Milena Rutkowski, Piotr Oncol Lett Articles Giant cell tumor of bone (GCTB) is an osteolytic, locally aggressive tumor that rarely metastasizes and typically occurs in the bones. At present, the primary treatment for GCTB is curettage with local adjuvants. Giant cells express receptor activator of nuclear factor-κB ligand (RANKL). Denosumab, a RANKL inhibitor appears to present an effective therapeutic option in advanced cases of GCTB. The aim of the present study was to confirm the efficacy of denosumab in large group of patients with locally advanced GCTB. A total of 35 patients with histologically confirmed GCTB that were treated with denosumab with no participation in clinical trials between May 2013 and September 2015 were included in the present study. Denosumab treatment was administered until complete tumor resection was feasible or tumor progression or unacceptable toxicity had occurred. The mean denosumab treatment duration was 7.4 months. A total of 17 patients received surgery following denosumab treatment: 11 patients underwent wide en bloc resection with prosthesis implantation in 10 cases and 6 patients were treated with intralesional curettage. Tumor progression was observed in 2 patients that underwent intralesional curettage without prosthesis implantation. In addition, tumor progression was observed during denosumab treatment in 2 patients that had previously undergone radiotherapy. The overall 1-year progression-free survival rate was 92.8%. Thus, for patients with advanced, unresectable, progressive or symptomatic pretreated GCTB, denosumab provides a therapeutic option not previously available, which has become the standard therapy in multidisciplinary management of GCTB. D.A. Spandidos 2016-12 2016-10-12 /pmc/articles/PMC5228072/ /pubmed/28101196 http://dx.doi.org/10.3892/ol.2016.5246 Text en Copyright: © Borkowska et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Borkowska, Aneta
Goryń, Tomasz
Pieńkowski, Andrzej
Wągrodzki, Michał
Jagiełło-Wieczorek, Ewelina
Rogala, Paweł
Szacht, Milena
Rutkowski, Piotr
Denosumab treatment of inoperable or locally advanced giant cell tumor of bone
title Denosumab treatment of inoperable or locally advanced giant cell tumor of bone
title_full Denosumab treatment of inoperable or locally advanced giant cell tumor of bone
title_fullStr Denosumab treatment of inoperable or locally advanced giant cell tumor of bone
title_full_unstemmed Denosumab treatment of inoperable or locally advanced giant cell tumor of bone
title_short Denosumab treatment of inoperable or locally advanced giant cell tumor of bone
title_sort denosumab treatment of inoperable or locally advanced giant cell tumor of bone
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5228072/
https://www.ncbi.nlm.nih.gov/pubmed/28101196
http://dx.doi.org/10.3892/ol.2016.5246
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