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The prognostic value of the C-reactive protein to albumin ratio in cancer: An updated meta-analysis
BACKGROUND: Previous studies have demonstrated that the C-reactive protein to albumin ratio (CAR) is correlated with the clinical outcomes of solid tumors. However, the available data have not been systematically evaluated. The objective of the present meta-analysis was to explore the prognostic val...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220550/ https://www.ncbi.nlm.nih.gov/pubmed/32243358 http://dx.doi.org/10.1097/MD.0000000000019165 |
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author | Cui, Xinhua Jia, Zhiqiang Chen, Dingchao Xu, Chunwei Yang, Peng |
author_facet | Cui, Xinhua Jia, Zhiqiang Chen, Dingchao Xu, Chunwei Yang, Peng |
author_sort | Cui, Xinhua |
collection | PubMed |
description | BACKGROUND: Previous studies have demonstrated that the C-reactive protein to albumin ratio (CAR) is correlated with the clinical outcomes of solid tumors. However, the available data have not been systematically evaluated. The objective of the present meta-analysis was to explore the prognostic value of the CAR in solid tumors. METHODS: Eligible studies were identified from the PubMed, EMBASE and Web of Science electronic databases. The clinical characteristics, disease -free survival (DFS) /progression-free survival (PFS) and overall survival (OS) were extracted from the eligible studies. The pooled hazard ratios (HRs) and 95% confidence intervals were calculated with STATA 12.0 software. We also performed subgroup, meta-regression and sensitivity analyses. RESULTS: In total, twenty-seven eligible studies including 10556 patients were enrolled in the present meta-analysis. The pooled HRs with 95% confidence intervals showed that the CAR was significantly associated with poor OS (HR = 1.95, 95% CI: 1.71–2.22) and DFS/PFS (HR = 1.82, 95% CI: 1.61–2.07) in patients with solid tumors. Although publication bias was found in the studies with regard to OS, a further trim and fill analysis revealed that the adjusted HR was 1.82 (95% CI: 1.69–1.96), which was close to the original HR. Subgroup analysis confirmed the CAR as a strong prognostic marker in patients with solid tumors, regardless of the tumor type, detection time, cut-off value, sample size and area. CONCLUSION: Our meta-analysis indicated that a high CAR might be an unfavorable prognostic marker for OS and DFS/PFS in patients with solid tumors. |
format | Online Article Text |
id | pubmed-7220550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-72205502020-06-15 The prognostic value of the C-reactive protein to albumin ratio in cancer: An updated meta-analysis Cui, Xinhua Jia, Zhiqiang Chen, Dingchao Xu, Chunwei Yang, Peng Medicine (Baltimore) 5700 BACKGROUND: Previous studies have demonstrated that the C-reactive protein to albumin ratio (CAR) is correlated with the clinical outcomes of solid tumors. However, the available data have not been systematically evaluated. The objective of the present meta-analysis was to explore the prognostic value of the CAR in solid tumors. METHODS: Eligible studies were identified from the PubMed, EMBASE and Web of Science electronic databases. The clinical characteristics, disease -free survival (DFS) /progression-free survival (PFS) and overall survival (OS) were extracted from the eligible studies. The pooled hazard ratios (HRs) and 95% confidence intervals were calculated with STATA 12.0 software. We also performed subgroup, meta-regression and sensitivity analyses. RESULTS: In total, twenty-seven eligible studies including 10556 patients were enrolled in the present meta-analysis. The pooled HRs with 95% confidence intervals showed that the CAR was significantly associated with poor OS (HR = 1.95, 95% CI: 1.71–2.22) and DFS/PFS (HR = 1.82, 95% CI: 1.61–2.07) in patients with solid tumors. Although publication bias was found in the studies with regard to OS, a further trim and fill analysis revealed that the adjusted HR was 1.82 (95% CI: 1.69–1.96), which was close to the original HR. Subgroup analysis confirmed the CAR as a strong prognostic marker in patients with solid tumors, regardless of the tumor type, detection time, cut-off value, sample size and area. CONCLUSION: Our meta-analysis indicated that a high CAR might be an unfavorable prognostic marker for OS and DFS/PFS in patients with solid tumors. Wolters Kluwer Health 2020-04-03 /pmc/articles/PMC7220550/ /pubmed/32243358 http://dx.doi.org/10.1097/MD.0000000000019165 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 5700 Cui, Xinhua Jia, Zhiqiang Chen, Dingchao Xu, Chunwei Yang, Peng The prognostic value of the C-reactive protein to albumin ratio in cancer: An updated meta-analysis |
title | The prognostic value of the C-reactive protein to albumin ratio in cancer: An updated meta-analysis |
title_full | The prognostic value of the C-reactive protein to albumin ratio in cancer: An updated meta-analysis |
title_fullStr | The prognostic value of the C-reactive protein to albumin ratio in cancer: An updated meta-analysis |
title_full_unstemmed | The prognostic value of the C-reactive protein to albumin ratio in cancer: An updated meta-analysis |
title_short | The prognostic value of the C-reactive protein to albumin ratio in cancer: An updated meta-analysis |
title_sort | prognostic value of the c-reactive protein to albumin ratio in cancer: an updated meta-analysis |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220550/ https://www.ncbi.nlm.nih.gov/pubmed/32243358 http://dx.doi.org/10.1097/MD.0000000000019165 |
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