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Modified Glasgow prognostic score as a prognostic factor for renal cell carcinomas: a systematic review and meta-analysis
OBJECTIVE: The modified Glasgow prognostic score (mGPS), a combination of C-reactive protein (CRP) and albumin levels, reflects systemic inflammation and nutritional status. This score has been shown to have prognosis value for various tumors. In the present study, we evaluated the prognostic value...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613602/ https://www.ncbi.nlm.nih.gov/pubmed/31308752 http://dx.doi.org/10.2147/CMAR.S208839 |
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author | Hu, Xu Wang, Yan Yang, Wei-Xiao Dou, Wei-Chao Shao, Yan-Xiang Li, Xiang |
author_facet | Hu, Xu Wang, Yan Yang, Wei-Xiao Dou, Wei-Chao Shao, Yan-Xiang Li, Xiang |
author_sort | Hu, Xu |
collection | PubMed |
description | OBJECTIVE: The modified Glasgow prognostic score (mGPS), a combination of C-reactive protein (CRP) and albumin levels, reflects systemic inflammation and nutritional status. This score has been shown to have prognosis value for various tumors. In the present study, we evaluated the prognostic value of mGPS for patients with renal cell carcinoma (RCC). METHODS: Literature search was conducted based on PubMed, Embase, and Cochrane Central Register of Controlled Trials up to December 2018. We pooled HRs and 95% CIs to evaluate the correlation between mGPS and survival in patients with RCC. RESULTS: Twelve studies comprising 2,391 patients were included in the present study for quantitative synthesis. Our studies demonstrated that higher mGPS was significantly correlated to poor overall survival (HR=4.31; 95%CI, 2.78–6.68; P<0.001), cancer-specific survival (HR=5.88; 95%CI, 3.93–8.78; P<0.001), recurrence-free survival (HR=3.15; 95%CI, 2.07–4.79; P<0.001), and progression-free survival (HR=1.91; 95%CI, 1.27–2.89; P=0.002). Subgroup analyses also confirmed the overall results. CONCLUSION: mGPS could serve as a predictive tool for the survival of patients with RCC. In the different subgroups, the results are also consistent with previous results. In conclusion, pretreatment higher mGPS is associated with poorer survival in patients with RCC. Further external validations are necessary to strengthen this concept. |
format | Online Article Text |
id | pubmed-6613602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-66136022019-07-15 Modified Glasgow prognostic score as a prognostic factor for renal cell carcinomas: a systematic review and meta-analysis Hu, Xu Wang, Yan Yang, Wei-Xiao Dou, Wei-Chao Shao, Yan-Xiang Li, Xiang Cancer Manag Res Review OBJECTIVE: The modified Glasgow prognostic score (mGPS), a combination of C-reactive protein (CRP) and albumin levels, reflects systemic inflammation and nutritional status. This score has been shown to have prognosis value for various tumors. In the present study, we evaluated the prognostic value of mGPS for patients with renal cell carcinoma (RCC). METHODS: Literature search was conducted based on PubMed, Embase, and Cochrane Central Register of Controlled Trials up to December 2018. We pooled HRs and 95% CIs to evaluate the correlation between mGPS and survival in patients with RCC. RESULTS: Twelve studies comprising 2,391 patients were included in the present study for quantitative synthesis. Our studies demonstrated that higher mGPS was significantly correlated to poor overall survival (HR=4.31; 95%CI, 2.78–6.68; P<0.001), cancer-specific survival (HR=5.88; 95%CI, 3.93–8.78; P<0.001), recurrence-free survival (HR=3.15; 95%CI, 2.07–4.79; P<0.001), and progression-free survival (HR=1.91; 95%CI, 1.27–2.89; P=0.002). Subgroup analyses also confirmed the overall results. CONCLUSION: mGPS could serve as a predictive tool for the survival of patients with RCC. In the different subgroups, the results are also consistent with previous results. In conclusion, pretreatment higher mGPS is associated with poorer survival in patients with RCC. Further external validations are necessary to strengthen this concept. Dove 2019-07-04 /pmc/articles/PMC6613602/ /pubmed/31308752 http://dx.doi.org/10.2147/CMAR.S208839 Text en © 2019 Hu et al. http://creativecommons.org/licenses/by-nc/3.0/ 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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Hu, Xu Wang, Yan Yang, Wei-Xiao Dou, Wei-Chao Shao, Yan-Xiang Li, Xiang Modified Glasgow prognostic score as a prognostic factor for renal cell carcinomas: a systematic review and meta-analysis |
title | Modified Glasgow prognostic score as a prognostic factor for renal cell carcinomas: a systematic review and meta-analysis |
title_full | Modified Glasgow prognostic score as a prognostic factor for renal cell carcinomas: a systematic review and meta-analysis |
title_fullStr | Modified Glasgow prognostic score as a prognostic factor for renal cell carcinomas: a systematic review and meta-analysis |
title_full_unstemmed | Modified Glasgow prognostic score as a prognostic factor for renal cell carcinomas: a systematic review and meta-analysis |
title_short | Modified Glasgow prognostic score as a prognostic factor for renal cell carcinomas: a systematic review and meta-analysis |
title_sort | modified glasgow prognostic score as a prognostic factor for renal cell carcinomas: a systematic review and meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613602/ https://www.ncbi.nlm.nih.gov/pubmed/31308752 http://dx.doi.org/10.2147/CMAR.S208839 |
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