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The prognostic value of modified Glasgow Prognostic Score in pancreatic cancer: a meta-analysis
BACKGROUND: Several studies were conducted to explore the prognostic value of modified Glasgow Prognostic Score (mGPS) in pancreatic cancer, which reported contradictory results. The purpose of this meta-analysis was to summarize and further investigate the correlation between mGPS and overall survi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510124/ https://www.ncbi.nlm.nih.gov/pubmed/32982584 http://dx.doi.org/10.1186/s12935-020-01558-4 |
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author | Zhang, Huan Ren, Dianyun Jin, Xin Wu, Heshui |
author_facet | Zhang, Huan Ren, Dianyun Jin, Xin Wu, Heshui |
author_sort | Zhang, Huan |
collection | PubMed |
description | BACKGROUND: Several studies were conducted to explore the prognostic value of modified Glasgow Prognostic Score (mGPS) in pancreatic cancer, which reported contradictory results. The purpose of this meta-analysis was to summarize and further investigate the correlation between mGPS and overall survival (OS) in pancreatic cancer. METHODS: A systematic literature search was performed in PubMed, EMBASE, ISI Web of Science, Cochrane library databases and OVID to identify eligible studies published from Jan 1, 2011 to June 20, 2020. Pooled hazard ratios (HRs) with corresponding 95% confidence intervals (CIs) were used to detect the prognostic significance of mGPS in patients with pancreatic cancer. RESULTS: A total of 222 non-repetitive studies were identified, and 20 related studies that explored the association between survival outcomes and mGPS in pancreatic cancer patients were finally enrolled in this meta-analysis. The results showed a significant correlation between high level of mGPS and poor OS (HR = 1.50, 95% CI 1.20–1.89, P < 0.0001). Similar results were observed in the subgroup analyses based on the treatment regimen and research region. CONCLUSIONS: Our study suggested the close association between poor prognosis and high level of mGPS, which will be helpful for future clinical applications in patients with pancreatic cancer. |
format | Online Article Text |
id | pubmed-7510124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75101242020-09-24 The prognostic value of modified Glasgow Prognostic Score in pancreatic cancer: a meta-analysis Zhang, Huan Ren, Dianyun Jin, Xin Wu, Heshui Cancer Cell Int Primary Research BACKGROUND: Several studies were conducted to explore the prognostic value of modified Glasgow Prognostic Score (mGPS) in pancreatic cancer, which reported contradictory results. The purpose of this meta-analysis was to summarize and further investigate the correlation between mGPS and overall survival (OS) in pancreatic cancer. METHODS: A systematic literature search was performed in PubMed, EMBASE, ISI Web of Science, Cochrane library databases and OVID to identify eligible studies published from Jan 1, 2011 to June 20, 2020. Pooled hazard ratios (HRs) with corresponding 95% confidence intervals (CIs) were used to detect the prognostic significance of mGPS in patients with pancreatic cancer. RESULTS: A total of 222 non-repetitive studies were identified, and 20 related studies that explored the association between survival outcomes and mGPS in pancreatic cancer patients were finally enrolled in this meta-analysis. The results showed a significant correlation between high level of mGPS and poor OS (HR = 1.50, 95% CI 1.20–1.89, P < 0.0001). Similar results were observed in the subgroup analyses based on the treatment regimen and research region. CONCLUSIONS: Our study suggested the close association between poor prognosis and high level of mGPS, which will be helpful for future clinical applications in patients with pancreatic cancer. BioMed Central 2020-09-22 /pmc/articles/PMC7510124/ /pubmed/32982584 http://dx.doi.org/10.1186/s12935-020-01558-4 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 | Primary Research Zhang, Huan Ren, Dianyun Jin, Xin Wu, Heshui The prognostic value of modified Glasgow Prognostic Score in pancreatic cancer: a meta-analysis |
title | The prognostic value of modified Glasgow Prognostic Score in pancreatic cancer: a meta-analysis |
title_full | The prognostic value of modified Glasgow Prognostic Score in pancreatic cancer: a meta-analysis |
title_fullStr | The prognostic value of modified Glasgow Prognostic Score in pancreatic cancer: a meta-analysis |
title_full_unstemmed | The prognostic value of modified Glasgow Prognostic Score in pancreatic cancer: a meta-analysis |
title_short | The prognostic value of modified Glasgow Prognostic Score in pancreatic cancer: a meta-analysis |
title_sort | prognostic value of modified glasgow prognostic score in pancreatic cancer: a meta-analysis |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510124/ https://www.ncbi.nlm.nih.gov/pubmed/32982584 http://dx.doi.org/10.1186/s12935-020-01558-4 |
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