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Clear cell chondrosarcoma is an underestimated tumor: Report of 7 cases and meta-analysis of the literature
INTRODUCTION: Clear cell chondrosarcoma (CCC) is a rare subtype of chondrosarcoma and it is commonly considered a low-grade tumor and less aggressive than atypical cartilaginous tumor (grade 1 central chondrosarcoma). However, the experience even of musculoskeletal tumor centres with this rare entit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879987/ https://www.ncbi.nlm.nih.gov/pubmed/31788417 http://dx.doi.org/10.1016/j.jbo.2019.100267 |
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author | Klein, Alexander Tauscher, Felix Birkenmaier, Christof Baur-Melnyk, Andrea Knösel, Thomas Jansson, Volkmar Dürr, Hans Roland |
author_facet | Klein, Alexander Tauscher, Felix Birkenmaier, Christof Baur-Melnyk, Andrea Knösel, Thomas Jansson, Volkmar Dürr, Hans Roland |
author_sort | Klein, Alexander |
collection | PubMed |
description | INTRODUCTION: Clear cell chondrosarcoma (CCC) is a rare subtype of chondrosarcoma and it is commonly considered a low-grade tumor and less aggressive than atypical cartilaginous tumor (grade 1 central chondrosarcoma). However, the experience even of musculoskeletal tumor centres with this rare entity is limited. The aim of this study is to analyse our own treatment results and those of the literature regarding the therapy and outcome of this lesion. MATERIAL AND METHODS: 7 cases of CCC have been treated in our department between 2003 and 2015. Their follow-up data were collected retrospectively. 187 literature cases with histopathological and clinical characteristics were retrieved by means of a PubMed search with the key word “clear cell chondrosarcoma”. The data pertaining to treatment and follow up were extracted. We analysed the survival of patient and the risk factors for local recurrence (LR) as well as metastatic disease (MD). RESULTS: The mean age at the time of diagnosis was 40 years. Two thirds of the patients were male. The mean follow-up time was 109 months. To our surprise, there was a high rate of LR (30%) and of MD (20%) when compared to low-grade conventional chondrosarcomas. 15% of LR and 20% of metastatic disease were observed after more than 10 years follow-up. Uncommon locations of MD such as in the spine is a unique observation in chondrosarcomas and underlines the high aggressiveness of this tumor. 10-year overall survival was almost 80%, 10-years disease free survival 60%. Positive margins (p = 0.038) and metastases (p = 0.006) impaired the overall survival significantly. The rate of local recurrence was significantly dependent on resection margin (p < 0.001); however there was no correlation with the grade of differentiation of the tumor. The development of MD was affected by local recurrence (p = 0.006), but we could not detect a significant association with margin status (p = 0.184). CONCLUSIONS: A wide resection is the advocated treatment option. Long term follow-up for at least 10 years is necessary in order to not overlook late LR or MD. This work demonstrates for the first time the apparent aggressiveness of the CCC. |
format | Online Article Text |
id | pubmed-6879987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68799872019-11-29 Clear cell chondrosarcoma is an underestimated tumor: Report of 7 cases and meta-analysis of the literature Klein, Alexander Tauscher, Felix Birkenmaier, Christof Baur-Melnyk, Andrea Knösel, Thomas Jansson, Volkmar Dürr, Hans Roland J Bone Oncol Research Article INTRODUCTION: Clear cell chondrosarcoma (CCC) is a rare subtype of chondrosarcoma and it is commonly considered a low-grade tumor and less aggressive than atypical cartilaginous tumor (grade 1 central chondrosarcoma). However, the experience even of musculoskeletal tumor centres with this rare entity is limited. The aim of this study is to analyse our own treatment results and those of the literature regarding the therapy and outcome of this lesion. MATERIAL AND METHODS: 7 cases of CCC have been treated in our department between 2003 and 2015. Their follow-up data were collected retrospectively. 187 literature cases with histopathological and clinical characteristics were retrieved by means of a PubMed search with the key word “clear cell chondrosarcoma”. The data pertaining to treatment and follow up were extracted. We analysed the survival of patient and the risk factors for local recurrence (LR) as well as metastatic disease (MD). RESULTS: The mean age at the time of diagnosis was 40 years. Two thirds of the patients were male. The mean follow-up time was 109 months. To our surprise, there was a high rate of LR (30%) and of MD (20%) when compared to low-grade conventional chondrosarcomas. 15% of LR and 20% of metastatic disease were observed after more than 10 years follow-up. Uncommon locations of MD such as in the spine is a unique observation in chondrosarcomas and underlines the high aggressiveness of this tumor. 10-year overall survival was almost 80%, 10-years disease free survival 60%. Positive margins (p = 0.038) and metastases (p = 0.006) impaired the overall survival significantly. The rate of local recurrence was significantly dependent on resection margin (p < 0.001); however there was no correlation with the grade of differentiation of the tumor. The development of MD was affected by local recurrence (p = 0.006), but we could not detect a significant association with margin status (p = 0.184). CONCLUSIONS: A wide resection is the advocated treatment option. Long term follow-up for at least 10 years is necessary in order to not overlook late LR or MD. This work demonstrates for the first time the apparent aggressiveness of the CCC. Elsevier 2019-10-31 /pmc/articles/PMC6879987/ /pubmed/31788417 http://dx.doi.org/10.1016/j.jbo.2019.100267 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Klein, Alexander Tauscher, Felix Birkenmaier, Christof Baur-Melnyk, Andrea Knösel, Thomas Jansson, Volkmar Dürr, Hans Roland Clear cell chondrosarcoma is an underestimated tumor: Report of 7 cases and meta-analysis of the literature |
title | Clear cell chondrosarcoma is an underestimated tumor: Report of 7 cases and meta-analysis of the literature |
title_full | Clear cell chondrosarcoma is an underestimated tumor: Report of 7 cases and meta-analysis of the literature |
title_fullStr | Clear cell chondrosarcoma is an underestimated tumor: Report of 7 cases and meta-analysis of the literature |
title_full_unstemmed | Clear cell chondrosarcoma is an underestimated tumor: Report of 7 cases and meta-analysis of the literature |
title_short | Clear cell chondrosarcoma is an underestimated tumor: Report of 7 cases and meta-analysis of the literature |
title_sort | clear cell chondrosarcoma is an underestimated tumor: report of 7 cases and meta-analysis of the literature |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879987/ https://www.ncbi.nlm.nih.gov/pubmed/31788417 http://dx.doi.org/10.1016/j.jbo.2019.100267 |
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