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Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone
BACKGROUND: Giant cell tumour of bone (GCTB) is an expansile osteolytic tumour which contains numerous osteoclast-like giant cells. GCTB frequently recurs and can produce metastatic lesions in the lungs. Bisphosphonates are anti-resorptive drugs which act mainly on osteoclasts. METHOD: In this study...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940802/ https://www.ncbi.nlm.nih.gov/pubmed/20799989 http://dx.doi.org/10.1186/1471-2407-10-462 |
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author | Balke, Maurice Campanacci, Laura Gebert, Carsten Picci, Piero Gibbons, Max Taylor, Richard Hogendoorn, Pancras Kroep, Judith Wass, John Athanasou, Nicholas |
author_facet | Balke, Maurice Campanacci, Laura Gebert, Carsten Picci, Piero Gibbons, Max Taylor, Richard Hogendoorn, Pancras Kroep, Judith Wass, John Athanasou, Nicholas |
author_sort | Balke, Maurice |
collection | PubMed |
description | BACKGROUND: Giant cell tumour of bone (GCTB) is an expansile osteolytic tumour which contains numerous osteoclast-like giant cells. GCTB frequently recurs and can produce metastatic lesions in the lungs. Bisphosphonates are anti-resorptive drugs which act mainly on osteoclasts. METHOD: In this study, we have examined clinical and radiological outcomes of treatment with aminobisphosphonates on 25 cases of aggressive primary, recurrent and metastatic GCTB derived from four European centres. We also analysed in vitro the inhibitory effect of zoledronic acid on osteoclasts isolated from GCTBs. RESULTS: Treatment protocols differed with several different aminobisphosphonates being employed, but stabilisation of disease was achieved in most of these cases which were refractory to conventional treatment. Most inoperable sacral/pelvic tumours did not increase in size and no further recurrence was seen in GCTBs that had repeatedly recurred in bone and soft tissues. Lung metastases did not increase in size or number following treatment. Zoledronic acid markedly inhibited lacunar resorption by GCTB-derived osteoclasts in vitro. CONCLUSION: Our findings suggest that bisphosphonates may be useful in controlling disease progression in GCTB and that these agents directly inhibit GCTB - derived osteoclast resorption. These studies highlight the need for the establishment of standardised protocols to assess the efficacy of bisphosphonate treatment of GCTB. |
format | Text |
id | pubmed-2940802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29408022010-09-17 Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone Balke, Maurice Campanacci, Laura Gebert, Carsten Picci, Piero Gibbons, Max Taylor, Richard Hogendoorn, Pancras Kroep, Judith Wass, John Athanasou, Nicholas BMC Cancer Research Article BACKGROUND: Giant cell tumour of bone (GCTB) is an expansile osteolytic tumour which contains numerous osteoclast-like giant cells. GCTB frequently recurs and can produce metastatic lesions in the lungs. Bisphosphonates are anti-resorptive drugs which act mainly on osteoclasts. METHOD: In this study, we have examined clinical and radiological outcomes of treatment with aminobisphosphonates on 25 cases of aggressive primary, recurrent and metastatic GCTB derived from four European centres. We also analysed in vitro the inhibitory effect of zoledronic acid on osteoclasts isolated from GCTBs. RESULTS: Treatment protocols differed with several different aminobisphosphonates being employed, but stabilisation of disease was achieved in most of these cases which were refractory to conventional treatment. Most inoperable sacral/pelvic tumours did not increase in size and no further recurrence was seen in GCTBs that had repeatedly recurred in bone and soft tissues. Lung metastases did not increase in size or number following treatment. Zoledronic acid markedly inhibited lacunar resorption by GCTB-derived osteoclasts in vitro. CONCLUSION: Our findings suggest that bisphosphonates may be useful in controlling disease progression in GCTB and that these agents directly inhibit GCTB - derived osteoclast resorption. These studies highlight the need for the establishment of standardised protocols to assess the efficacy of bisphosphonate treatment of GCTB. BioMed Central 2010-08-29 /pmc/articles/PMC2940802/ /pubmed/20799989 http://dx.doi.org/10.1186/1471-2407-10-462 Text en Copyright ©2010 Balke et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Balke, Maurice Campanacci, Laura Gebert, Carsten Picci, Piero Gibbons, Max Taylor, Richard Hogendoorn, Pancras Kroep, Judith Wass, John Athanasou, Nicholas Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone |
title | Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone |
title_full | Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone |
title_fullStr | Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone |
title_full_unstemmed | Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone |
title_short | Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone |
title_sort | bisphosphonate treatment of aggressive primary, recurrent and metastatic giant cell tumour of bone |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940802/ https://www.ncbi.nlm.nih.gov/pubmed/20799989 http://dx.doi.org/10.1186/1471-2407-10-462 |
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