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Prognostic value of (18)F-FDG-PET/CT in patients with nasopharyngeal carcinoma: a systematic review and meta-analysis
BACKGROUND: The prognostic role of (18)F-fluorodeoxyglucose positron emission tomography CT ((18)F-FDG PET/CT) parameters is still controversial in nasopharyngeal carcinoma patients. We sought to perform a systematic review and meta-analysis to explore the prognostic value of maximal standardized up...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5464920/ https://www.ncbi.nlm.nih.gov/pubmed/27980228 http://dx.doi.org/10.18632/oncotarget.13934 |
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author | Lin, Jie Xie, Guozhu Liao, Guixiang Wang, Baiyao Yan, Miaohong Li, Hui Yuan, Yawei |
author_facet | Lin, Jie Xie, Guozhu Liao, Guixiang Wang, Baiyao Yan, Miaohong Li, Hui Yuan, Yawei |
author_sort | Lin, Jie |
collection | PubMed |
description | BACKGROUND: The prognostic role of (18)F-fluorodeoxyglucose positron emission tomography CT ((18)F-FDG PET/CT) parameters is still controversial in nasopharyngeal carcinoma patients. We sought to perform a systematic review and meta-analysis to explore the prognostic value of maximal standardized uptake value (SUV(max)), metabolic tumor volume (MTV) and total lesion glycolysis (TLG) on event-free survival (EFS) and overall survival (OS) in nasopharyngeal carcinoma patients. RESULTS: Fifteen studies comprising 1,938 patients were included in this study. The combined hazard ratios (HRs) for EFS were 2.63 (95%CI 1.71-4.05) for SUV(max), 2.55 (95%CI 1.49-4.35) for MTV, and 3.32 (95%CI 1.23-8.95) for TLG. The pooled HRs for OS were 2.07 (95%CI 1.54-2.79) for SUV(max), 3.86 (95%CI 1.85-8.06) for MTV, and 2.60 (95%CI 1.55-4.34) for TLG. The prognostic role of SUV(max), MTV and TLG remained similar in the sub-group analyses. METHODS: A systematic literature search was performed to identify studies which associated (18)F-FDG PET/CT to clinical survival outcomes of nasopharyngeal carcinoma patients. The summarized HRs for EFS and OS were estimated by using fixed- or random-effect models according to heterogeneity between trials. CONCLUSIONS: The present meta-analysis confirms that high values of SUV(max), MTV and TLG predicted a higher risk of adverse events or death in patients with nasopharyngeal carcinoma, despite clinically heterogeneous nasopharyngeal carcinoma patients and the various methods adopted between these studies. |
format | Online Article Text |
id | pubmed-5464920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-54649202017-06-21 Prognostic value of (18)F-FDG-PET/CT in patients with nasopharyngeal carcinoma: a systematic review and meta-analysis Lin, Jie Xie, Guozhu Liao, Guixiang Wang, Baiyao Yan, Miaohong Li, Hui Yuan, Yawei Oncotarget Review BACKGROUND: The prognostic role of (18)F-fluorodeoxyglucose positron emission tomography CT ((18)F-FDG PET/CT) parameters is still controversial in nasopharyngeal carcinoma patients. We sought to perform a systematic review and meta-analysis to explore the prognostic value of maximal standardized uptake value (SUV(max)), metabolic tumor volume (MTV) and total lesion glycolysis (TLG) on event-free survival (EFS) and overall survival (OS) in nasopharyngeal carcinoma patients. RESULTS: Fifteen studies comprising 1,938 patients were included in this study. The combined hazard ratios (HRs) for EFS were 2.63 (95%CI 1.71-4.05) for SUV(max), 2.55 (95%CI 1.49-4.35) for MTV, and 3.32 (95%CI 1.23-8.95) for TLG. The pooled HRs for OS were 2.07 (95%CI 1.54-2.79) for SUV(max), 3.86 (95%CI 1.85-8.06) for MTV, and 2.60 (95%CI 1.55-4.34) for TLG. The prognostic role of SUV(max), MTV and TLG remained similar in the sub-group analyses. METHODS: A systematic literature search was performed to identify studies which associated (18)F-FDG PET/CT to clinical survival outcomes of nasopharyngeal carcinoma patients. The summarized HRs for EFS and OS were estimated by using fixed- or random-effect models according to heterogeneity between trials. CONCLUSIONS: The present meta-analysis confirms that high values of SUV(max), MTV and TLG predicted a higher risk of adverse events or death in patients with nasopharyngeal carcinoma, despite clinically heterogeneous nasopharyngeal carcinoma patients and the various methods adopted between these studies. Impact Journals LLC 2016-12-14 /pmc/articles/PMC5464920/ /pubmed/27980228 http://dx.doi.org/10.18632/oncotarget.13934 Text en Copyright: © 2017 Lin et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Review Lin, Jie Xie, Guozhu Liao, Guixiang Wang, Baiyao Yan, Miaohong Li, Hui Yuan, Yawei Prognostic value of (18)F-FDG-PET/CT in patients with nasopharyngeal carcinoma: a systematic review and meta-analysis |
title | Prognostic value of (18)F-FDG-PET/CT in patients with nasopharyngeal carcinoma: a systematic review and meta-analysis |
title_full | Prognostic value of (18)F-FDG-PET/CT in patients with nasopharyngeal carcinoma: a systematic review and meta-analysis |
title_fullStr | Prognostic value of (18)F-FDG-PET/CT in patients with nasopharyngeal carcinoma: a systematic review and meta-analysis |
title_full_unstemmed | Prognostic value of (18)F-FDG-PET/CT in patients with nasopharyngeal carcinoma: a systematic review and meta-analysis |
title_short | Prognostic value of (18)F-FDG-PET/CT in patients with nasopharyngeal carcinoma: a systematic review and meta-analysis |
title_sort | prognostic value of (18)f-fdg-pet/ct in patients with nasopharyngeal carcinoma: a systematic review and meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5464920/ https://www.ncbi.nlm.nih.gov/pubmed/27980228 http://dx.doi.org/10.18632/oncotarget.13934 |
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