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The utility of (18)F-FDG PET and PET/CT in the diagnosis and staging of chondrosarcoma: a meta-analysis

OBJECTIVE: Chondrosarcoma is the second most common primary bone sarcoma; however, unlike other tumors, the biopsy cannot easily make a definite diagnosis or predict the histological grade. This meta-analysis was performed to evaluate the utility of (18)F-FDG PET and PET/CT to differentiate chondros...

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Autores principales: Zhang, Qingyu, Xi, Yongming, Li, Dong, Yuan, Zenong, Dong, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310032/
https://www.ncbi.nlm.nih.gov/pubmed/32571371
http://dx.doi.org/10.1186/s13018-020-01748-w
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author Zhang, Qingyu
Xi, Yongming
Li, Dong
Yuan, Zenong
Dong, Jun
author_facet Zhang, Qingyu
Xi, Yongming
Li, Dong
Yuan, Zenong
Dong, Jun
author_sort Zhang, Qingyu
collection PubMed
description OBJECTIVE: Chondrosarcoma is the second most common primary bone sarcoma; however, unlike other tumors, the biopsy cannot easily make a definite diagnosis or predict the histological grade. This meta-analysis was performed to evaluate the utility of (18)F-FDG PET and PET/CT to differentiate chondrosarcoma from benign cartilaginous lesions and to predict the histopathological grade of chondrosarcoma. MATERIAL AND METHODS: A comprehensive search was performed in three electronic databases including Medline/PubMed, the Cochrane Library and Embase to retrieve diagnostic studies evaluating the role of (18)F-FDG PET or PET/CT for appraising the status of chondrosarcoma. Reference lists of related articles were also scrutinized manually. Useful data were extracted to calculate the pooled sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR), the summary receiver operating characteristic curve (sROC), and the area under the curve (AUC) of (18)F-FDG PET or PET/CT in diagnosing chondrosarcoma, and pooled weighted mean differences (WMD) of maximum standardized uptake value (SUVmax) between different entities of cartilaginous neoplasms by using Stata 19.0. RESULTS: A total of twelve studies provided sufficient data for the quantitative analysis. For the diagnosis of chondrosarcoma, the pooled sensitivity, specificity, and DOR of (18)F-FDG PET were 0.84 (95% confidence interval [CI] 0.46 to 0.97), 0.82 (95% CI 0.55 to 0.94), and 24.244 (95% CI 1.985 to 96.148), respectively while those of (18)F-FDG PET/CT were 0.94 (95% CI 0.86 to 0.97), 0.89 (95% CI 0.82 to 0.93), and 112.999 (95% CI 41.341 to 308.866), respectively. The pooled WMD of SUVmax were − 0.89 (95% CI −1.67 to −0.10) between benign cartilaginous lesions and grade 1 (G1) chondrosarcoma, −1.94 (95% CI −2.76 to −1.12) between G1 and grade 2 (G2) chondrosarcoma, and − 2.37 (95% CI −5.79 to 1.05) between G2 and grade 3 (G3) chondrosarcoma. CONCLUSIONS: In a word, (18)F-FDG PET/CT revealed excellent accuracy in the diagnosis of chondrosarcoma and might assist in clinical decision-making. Meanwhile, although SUVmax alone showed restricted ability to differentiate benign cartilaginous lesions and G1 chondrosarcoma, as well as between G2 and G3 chondrosarcoma, it can identify intermediate/high-grade chondrosarcoma from low-grade ones. LEVEL OF EVIDENCE: Level I evidence, a summary of meta-analysis
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spelling pubmed-73100322020-06-23 The utility of (18)F-FDG PET and PET/CT in the diagnosis and staging of chondrosarcoma: a meta-analysis Zhang, Qingyu Xi, Yongming Li, Dong Yuan, Zenong Dong, Jun J Orthop Surg Res Research Article OBJECTIVE: Chondrosarcoma is the second most common primary bone sarcoma; however, unlike other tumors, the biopsy cannot easily make a definite diagnosis or predict the histological grade. This meta-analysis was performed to evaluate the utility of (18)F-FDG PET and PET/CT to differentiate chondrosarcoma from benign cartilaginous lesions and to predict the histopathological grade of chondrosarcoma. MATERIAL AND METHODS: A comprehensive search was performed in three electronic databases including Medline/PubMed, the Cochrane Library and Embase to retrieve diagnostic studies evaluating the role of (18)F-FDG PET or PET/CT for appraising the status of chondrosarcoma. Reference lists of related articles were also scrutinized manually. Useful data were extracted to calculate the pooled sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR), the summary receiver operating characteristic curve (sROC), and the area under the curve (AUC) of (18)F-FDG PET or PET/CT in diagnosing chondrosarcoma, and pooled weighted mean differences (WMD) of maximum standardized uptake value (SUVmax) between different entities of cartilaginous neoplasms by using Stata 19.0. RESULTS: A total of twelve studies provided sufficient data for the quantitative analysis. For the diagnosis of chondrosarcoma, the pooled sensitivity, specificity, and DOR of (18)F-FDG PET were 0.84 (95% confidence interval [CI] 0.46 to 0.97), 0.82 (95% CI 0.55 to 0.94), and 24.244 (95% CI 1.985 to 96.148), respectively while those of (18)F-FDG PET/CT were 0.94 (95% CI 0.86 to 0.97), 0.89 (95% CI 0.82 to 0.93), and 112.999 (95% CI 41.341 to 308.866), respectively. The pooled WMD of SUVmax were − 0.89 (95% CI −1.67 to −0.10) between benign cartilaginous lesions and grade 1 (G1) chondrosarcoma, −1.94 (95% CI −2.76 to −1.12) between G1 and grade 2 (G2) chondrosarcoma, and − 2.37 (95% CI −5.79 to 1.05) between G2 and grade 3 (G3) chondrosarcoma. CONCLUSIONS: In a word, (18)F-FDG PET/CT revealed excellent accuracy in the diagnosis of chondrosarcoma and might assist in clinical decision-making. Meanwhile, although SUVmax alone showed restricted ability to differentiate benign cartilaginous lesions and G1 chondrosarcoma, as well as between G2 and G3 chondrosarcoma, it can identify intermediate/high-grade chondrosarcoma from low-grade ones. LEVEL OF EVIDENCE: Level I evidence, a summary of meta-analysis BioMed Central 2020-06-22 /pmc/articles/PMC7310032/ /pubmed/32571371 http://dx.doi.org/10.1186/s13018-020-01748-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Zhang, Qingyu
Xi, Yongming
Li, Dong
Yuan, Zenong
Dong, Jun
The utility of (18)F-FDG PET and PET/CT in the diagnosis and staging of chondrosarcoma: a meta-analysis
title The utility of (18)F-FDG PET and PET/CT in the diagnosis and staging of chondrosarcoma: a meta-analysis
title_full The utility of (18)F-FDG PET and PET/CT in the diagnosis and staging of chondrosarcoma: a meta-analysis
title_fullStr The utility of (18)F-FDG PET and PET/CT in the diagnosis and staging of chondrosarcoma: a meta-analysis
title_full_unstemmed The utility of (18)F-FDG PET and PET/CT in the diagnosis and staging of chondrosarcoma: a meta-analysis
title_short The utility of (18)F-FDG PET and PET/CT in the diagnosis and staging of chondrosarcoma: a meta-analysis
title_sort utility of (18)f-fdg pet and pet/ct in the diagnosis and staging of chondrosarcoma: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310032/
https://www.ncbi.nlm.nih.gov/pubmed/32571371
http://dx.doi.org/10.1186/s13018-020-01748-w
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