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Comprehensive analysis of published studies involving systemic treatment for chondrosarcoma of bone between 2000 and 2013
BACKGROUND: The majority of patients with chondrosarcoma of bone have an excellent overall survival after local therapy. However, in case of unresectable locally advanced or metastatic disease the outcome is poor and limited treatment options exist. Therefore we conducted a survey of clinical phase...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131227/ https://www.ncbi.nlm.nih.gov/pubmed/25126409 http://dx.doi.org/10.1186/2045-3329-4-11 |
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author | van Maldegem, Annemiek M Bovée, Judith VMG Gelderblom, Hans |
author_facet | van Maldegem, Annemiek M Bovée, Judith VMG Gelderblom, Hans |
author_sort | van Maldegem, Annemiek M |
collection | PubMed |
description | BACKGROUND: The majority of patients with chondrosarcoma of bone have an excellent overall survival after local therapy. However, in case of unresectable locally advanced or metastatic disease the outcome is poor and limited treatment options exist. Therefore we conducted a survey of clinical phase I or II trials and retrospective studies that described systemic therapy for chondrosarcoma patients. MATERIALS AND METHODS: Using PubMed, clinicaltrials.gov, the Cochrane controlled trial register and American Society of Clinical Oncology (ASCO) abstracts a literature survey was conducted. From the identified items, data were collected by a systematic analysis. We limited our search to semi-recent studies published between 2000 and 2013 to include modern drugs, imaging techniques and disease evaluations. RESULTS: A total of 31 studies were found which met the criteria: 9 phase I trials, 11 phase II and 8 retrospective studies. In these studies 855 chondrosarcoma patients were reported. The tested drugs were mostly non-cytotoxic, either alone or in combination with another non-cytotoxic agent or chemotherapy. Currently two phase I trials, one phase IB/II trial and three phase II trials are enrolling chondrosarcoma patients. CONCLUSION: Because chondrosarcoma of bone is an orphan disease it is difficult to conduct clinical trials. The meagre outcome data for locally advanced or metastatic patients indicate that new treatment options are needed. For the phase I trials it is difficult to draw conclusions because of the low numbers of chondrosarcoma patients enrolled, and at different dose levels. Some phase II trials show promising results which support further research. Retrospective studies are encouraged as they could add to the limited data available. Efforts to increase the number of studies for this orphan disease are urgently needed. |
format | Online Article Text |
id | pubmed-4131227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41312272014-08-15 Comprehensive analysis of published studies involving systemic treatment for chondrosarcoma of bone between 2000 and 2013 van Maldegem, Annemiek M Bovée, Judith VMG Gelderblom, Hans Clin Sarcoma Res Research BACKGROUND: The majority of patients with chondrosarcoma of bone have an excellent overall survival after local therapy. However, in case of unresectable locally advanced or metastatic disease the outcome is poor and limited treatment options exist. Therefore we conducted a survey of clinical phase I or II trials and retrospective studies that described systemic therapy for chondrosarcoma patients. MATERIALS AND METHODS: Using PubMed, clinicaltrials.gov, the Cochrane controlled trial register and American Society of Clinical Oncology (ASCO) abstracts a literature survey was conducted. From the identified items, data were collected by a systematic analysis. We limited our search to semi-recent studies published between 2000 and 2013 to include modern drugs, imaging techniques and disease evaluations. RESULTS: A total of 31 studies were found which met the criteria: 9 phase I trials, 11 phase II and 8 retrospective studies. In these studies 855 chondrosarcoma patients were reported. The tested drugs were mostly non-cytotoxic, either alone or in combination with another non-cytotoxic agent or chemotherapy. Currently two phase I trials, one phase IB/II trial and three phase II trials are enrolling chondrosarcoma patients. CONCLUSION: Because chondrosarcoma of bone is an orphan disease it is difficult to conduct clinical trials. The meagre outcome data for locally advanced or metastatic patients indicate that new treatment options are needed. For the phase I trials it is difficult to draw conclusions because of the low numbers of chondrosarcoma patients enrolled, and at different dose levels. Some phase II trials show promising results which support further research. Retrospective studies are encouraged as they could add to the limited data available. Efforts to increase the number of studies for this orphan disease are urgently needed. BioMed Central 2014-08-12 /pmc/articles/PMC4131227/ /pubmed/25126409 http://dx.doi.org/10.1186/2045-3329-4-11 Text en Copyright © 2014 van Maldegem et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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. |
spellingShingle | Research van Maldegem, Annemiek M Bovée, Judith VMG Gelderblom, Hans Comprehensive analysis of published studies involving systemic treatment for chondrosarcoma of bone between 2000 and 2013 |
title | Comprehensive analysis of published studies involving systemic treatment for chondrosarcoma of bone between 2000 and 2013 |
title_full | Comprehensive analysis of published studies involving systemic treatment for chondrosarcoma of bone between 2000 and 2013 |
title_fullStr | Comprehensive analysis of published studies involving systemic treatment for chondrosarcoma of bone between 2000 and 2013 |
title_full_unstemmed | Comprehensive analysis of published studies involving systemic treatment for chondrosarcoma of bone between 2000 and 2013 |
title_short | Comprehensive analysis of published studies involving systemic treatment for chondrosarcoma of bone between 2000 and 2013 |
title_sort | comprehensive analysis of published studies involving systemic treatment for chondrosarcoma of bone between 2000 and 2013 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131227/ https://www.ncbi.nlm.nih.gov/pubmed/25126409 http://dx.doi.org/10.1186/2045-3329-4-11 |
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