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Association between pretreatment Glasgow prognostic score and gastric cancer survival and clinicopathological features: a meta-analysis

BACKGROUND: Glasgow prognostic score (GPS) is widely known as a systemic inflammatory-based marker. The relationship between pretreatment GPS and gastric cancer (GC) survival and clinicopathological features remains controversial. The aim of the study was to conduct a meta-analysis of published stud...

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Autores principales: Zhang, Chun-Xiao, Wang, Shu-Yi, Chen, Shuang-Qian, Yang, Shuai-Long, Wan, Lu, Xiong, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930270/
https://www.ncbi.nlm.nih.gov/pubmed/27390529
http://dx.doi.org/10.2147/OTT.S103996
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author Zhang, Chun-Xiao
Wang, Shu-Yi
Chen, Shuang-Qian
Yang, Shuai-Long
Wan, Lu
Xiong, Bin
author_facet Zhang, Chun-Xiao
Wang, Shu-Yi
Chen, Shuang-Qian
Yang, Shuai-Long
Wan, Lu
Xiong, Bin
author_sort Zhang, Chun-Xiao
collection PubMed
description BACKGROUND: Glasgow prognostic score (GPS) is widely known as a systemic inflammatory-based marker. The relationship between pretreatment GPS and gastric cancer (GC) survival and clinicopathological features remains controversial. The aim of the study was to conduct a meta-analysis of published studies to evaluate the association between pretreatment GPS and survival and clinicopathological features in GC patients. METHODS: We searched PubMed, Embase, MEDLINE, and BioMed databases for relevant studies. Combined analyses were used to assess the association between pretreatment GPS and overall survival, disease-free survival, and clinicopathological parameters by Stata Version 12.0. RESULTS: A total of 14 studies were included in this meta-analysis, including 5,579 GC patients. The results indicated that pretreatment high GPS (HGPS) predicted poor overall survival (hazard ratio =1.51, 95% CI: 1.37–1.66, P<0.01) and disease-free survival (hazard ratio =1.45, 95% CI: 1.26–1.68, P<0.01) in GC patients. Pretreatment HGPS was also significantly associated with advanced tumor–node–metastasis stage (odds ratio [OR] =3.09, 95% CI: 2.11–4.53, P<0.01), lymph node metastasis (OR =4.60, 95% CI: 3.23–6.56, P<0.01), lymphatic invasion (OR =3.04, 95% CI: 2.00–4.62, P<0.01), and venous invasion (OR =3.56, 95% CI: 1.81–6.99, P<0.01). CONCLUSION: Our meta-analysis indicated that pretreatment HGPS could be a predicative factor of poor survival outcome and clinicopathological features for GC patients.
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spelling pubmed-49302702016-07-07 Association between pretreatment Glasgow prognostic score and gastric cancer survival and clinicopathological features: a meta-analysis Zhang, Chun-Xiao Wang, Shu-Yi Chen, Shuang-Qian Yang, Shuai-Long Wan, Lu Xiong, Bin Onco Targets Ther Original Research BACKGROUND: Glasgow prognostic score (GPS) is widely known as a systemic inflammatory-based marker. The relationship between pretreatment GPS and gastric cancer (GC) survival and clinicopathological features remains controversial. The aim of the study was to conduct a meta-analysis of published studies to evaluate the association between pretreatment GPS and survival and clinicopathological features in GC patients. METHODS: We searched PubMed, Embase, MEDLINE, and BioMed databases for relevant studies. Combined analyses were used to assess the association between pretreatment GPS and overall survival, disease-free survival, and clinicopathological parameters by Stata Version 12.0. RESULTS: A total of 14 studies were included in this meta-analysis, including 5,579 GC patients. The results indicated that pretreatment high GPS (HGPS) predicted poor overall survival (hazard ratio =1.51, 95% CI: 1.37–1.66, P<0.01) and disease-free survival (hazard ratio =1.45, 95% CI: 1.26–1.68, P<0.01) in GC patients. Pretreatment HGPS was also significantly associated with advanced tumor–node–metastasis stage (odds ratio [OR] =3.09, 95% CI: 2.11–4.53, P<0.01), lymph node metastasis (OR =4.60, 95% CI: 3.23–6.56, P<0.01), lymphatic invasion (OR =3.04, 95% CI: 2.00–4.62, P<0.01), and venous invasion (OR =3.56, 95% CI: 1.81–6.99, P<0.01). CONCLUSION: Our meta-analysis indicated that pretreatment HGPS could be a predicative factor of poor survival outcome and clinicopathological features for GC patients. Dove Medical Press 2016-06-27 /pmc/articles/PMC4930270/ /pubmed/27390529 http://dx.doi.org/10.2147/OTT.S103996 Text en © 2016 Zhang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Zhang, Chun-Xiao
Wang, Shu-Yi
Chen, Shuang-Qian
Yang, Shuai-Long
Wan, Lu
Xiong, Bin
Association between pretreatment Glasgow prognostic score and gastric cancer survival and clinicopathological features: a meta-analysis
title Association between pretreatment Glasgow prognostic score and gastric cancer survival and clinicopathological features: a meta-analysis
title_full Association between pretreatment Glasgow prognostic score and gastric cancer survival and clinicopathological features: a meta-analysis
title_fullStr Association between pretreatment Glasgow prognostic score and gastric cancer survival and clinicopathological features: a meta-analysis
title_full_unstemmed Association between pretreatment Glasgow prognostic score and gastric cancer survival and clinicopathological features: a meta-analysis
title_short Association between pretreatment Glasgow prognostic score and gastric cancer survival and clinicopathological features: a meta-analysis
title_sort association between pretreatment glasgow prognostic score and gastric cancer survival and clinicopathological features: a meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930270/
https://www.ncbi.nlm.nih.gov/pubmed/27390529
http://dx.doi.org/10.2147/OTT.S103996
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