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Prognostic value of the Glasgow prognostic score in colorectal cancer: a meta-analysis of 9,839 patients

PURPOSE: The aim of this study was to perform a systematic review and meta-analysis to evaluate the value of the Glasgow prognostic score (GPS) or modified Glasgow prognostic score (mGPS) in patients with colorectal cancer (CRC). METHODS: A comprehensive medical literature search was performed using...

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Autores principales: Lu, Xin, Guo, Wanying, Xu, Wei, Zhang, Xuelei, Shi, Zhijie, Zheng, Leizhen, Zhao, Wenzhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307678/
https://www.ncbi.nlm.nih.gov/pubmed/30636896
http://dx.doi.org/10.2147/CMAR.S185350
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author Lu, Xin
Guo, Wanying
Xu, Wei
Zhang, Xuelei
Shi, Zhijie
Zheng, Leizhen
Zhao, Wenzhao
author_facet Lu, Xin
Guo, Wanying
Xu, Wei
Zhang, Xuelei
Shi, Zhijie
Zheng, Leizhen
Zhao, Wenzhao
author_sort Lu, Xin
collection PubMed
description PURPOSE: The aim of this study was to perform a systematic review and meta-analysis to evaluate the value of the Glasgow prognostic score (GPS) or modified Glasgow prognostic score (mGPS) in patients with colorectal cancer (CRC). METHODS: A comprehensive medical literature search was performed using the online databases PubMed, Embase, Web of Science, and the Cochrane Library. After extracting basic characteristics and prognostic data from the included studies, overall survival (OS) and cancer-specific survival (CSS) were pooled as primary outcomes. Subgroup analyses were performed according to therapeutic strategies, models, cutoff values, regions, tumor, node, metastasis stages, sample size, and ages. RESULTS: Forty-three independent cohorts from 41 studies with 9,839 CRC patients were included in the present study. Correlation between GPS or mGPS and OS was analyzed in 32 cohorts of 7,714 patients, and 23 independent cohorts of 5,375 patients focused on the correlation between GPS or mGPS and CSS. The overall outcomes showed that patients with elevated GPS or mGPS were associated with poor OS (HR: 2.20, 95% CI: 1.88–2.57, P<0.001). Elevated GPS or mGPS also resulted in worse CSS (HR: 1.86, 95% CI: 1.59–2.17, P<0.001). The results of the subgroup analyses confirmed the overall outcomes. CONCLUSION: GPS or mGPS is an accurate prognostic predictor in patients with CRC. Patients with elevated pretreatment GPS or mGPS have a poor prognosis. Subgroup analyses confirmed the overall outcomes. Pretreatment GPS is a useful biomarker in the management of CRC.
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spelling pubmed-63076782019-01-11 Prognostic value of the Glasgow prognostic score in colorectal cancer: a meta-analysis of 9,839 patients Lu, Xin Guo, Wanying Xu, Wei Zhang, Xuelei Shi, Zhijie Zheng, Leizhen Zhao, Wenzhao Cancer Manag Res Original Research PURPOSE: The aim of this study was to perform a systematic review and meta-analysis to evaluate the value of the Glasgow prognostic score (GPS) or modified Glasgow prognostic score (mGPS) in patients with colorectal cancer (CRC). METHODS: A comprehensive medical literature search was performed using the online databases PubMed, Embase, Web of Science, and the Cochrane Library. After extracting basic characteristics and prognostic data from the included studies, overall survival (OS) and cancer-specific survival (CSS) were pooled as primary outcomes. Subgroup analyses were performed according to therapeutic strategies, models, cutoff values, regions, tumor, node, metastasis stages, sample size, and ages. RESULTS: Forty-three independent cohorts from 41 studies with 9,839 CRC patients were included in the present study. Correlation between GPS or mGPS and OS was analyzed in 32 cohorts of 7,714 patients, and 23 independent cohorts of 5,375 patients focused on the correlation between GPS or mGPS and CSS. The overall outcomes showed that patients with elevated GPS or mGPS were associated with poor OS (HR: 2.20, 95% CI: 1.88–2.57, P<0.001). Elevated GPS or mGPS also resulted in worse CSS (HR: 1.86, 95% CI: 1.59–2.17, P<0.001). The results of the subgroup analyses confirmed the overall outcomes. CONCLUSION: GPS or mGPS is an accurate prognostic predictor in patients with CRC. Patients with elevated pretreatment GPS or mGPS have a poor prognosis. Subgroup analyses confirmed the overall outcomes. Pretreatment GPS is a useful biomarker in the management of CRC. Dove Medical Press 2018-12-24 /pmc/articles/PMC6307678/ /pubmed/30636896 http://dx.doi.org/10.2147/CMAR.S185350 Text en © 2019 Lu 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
Lu, Xin
Guo, Wanying
Xu, Wei
Zhang, Xuelei
Shi, Zhijie
Zheng, Leizhen
Zhao, Wenzhao
Prognostic value of the Glasgow prognostic score in colorectal cancer: a meta-analysis of 9,839 patients
title Prognostic value of the Glasgow prognostic score in colorectal cancer: a meta-analysis of 9,839 patients
title_full Prognostic value of the Glasgow prognostic score in colorectal cancer: a meta-analysis of 9,839 patients
title_fullStr Prognostic value of the Glasgow prognostic score in colorectal cancer: a meta-analysis of 9,839 patients
title_full_unstemmed Prognostic value of the Glasgow prognostic score in colorectal cancer: a meta-analysis of 9,839 patients
title_short Prognostic value of the Glasgow prognostic score in colorectal cancer: a meta-analysis of 9,839 patients
title_sort prognostic value of the glasgow prognostic score in colorectal cancer: a meta-analysis of 9,839 patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307678/
https://www.ncbi.nlm.nih.gov/pubmed/30636896
http://dx.doi.org/10.2147/CMAR.S185350
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