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Prognostic role of platelet–lymphocyte ratio in colorectal cancer: A systematic review and meta-analysis

Many studies have been reported that platelet–lymphocyte ratio (PLR) may be associated with the prognosis of colorectal cancer (CRC), but the results are inconsistent. Current opinion on the prognostic role of the PLR in CRC is inconsistent and inconclusive. Therefore, we conduct a meta-analysis tha...

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Autores principales: Tan, Dewen, Fu, Yan, Su, Qi, Wang, Heling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998446/
https://www.ncbi.nlm.nih.gov/pubmed/27310960
http://dx.doi.org/10.1097/MD.0000000000003837
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author Tan, Dewen
Fu, Yan
Su, Qi
Wang, Heling
author_facet Tan, Dewen
Fu, Yan
Su, Qi
Wang, Heling
author_sort Tan, Dewen
collection PubMed
description Many studies have been reported that platelet–lymphocyte ratio (PLR) may be associated with the prognosis of colorectal cancer (CRC), but the results are inconsistent. Current opinion on the prognostic role of the PLR in CRC is inconsistent and inconclusive. Therefore, we conduct a meta-analysis that combines these studies and to identify the prognostic value of PLR in patients with CRC. Data were retrieved from PubMed, EMBASE, Cochrane Library, and Web of Science databases that came from inception through January 2016. We extracted data from the characteristics of each study and analyzed the relationship between PLR and overall survival (OS), disease-free survival (DFS), or other prognosis in patients with CRC by using the hazard ratio (HR) and 95% confidence intervals (95% CIs). Of the 256 identified studies, 15 studies were included and a total of 3991 patients were included. In a meta-analysis, patients with an elevated PLR had a significantly lower OS (pooled HR, 1.53; 95% CI, 1.24–1.89; P ≤ 0.001), DFS (pooled HR, 1.68; 95% CI, 1.07–2.62; P = 0.023). Even after sensitivity analyses and trim and fill method, high PLR remains significantly predictive poorer OS, but not DFS. In addition, our meta-analysis indicated that increased PLR is also significantly associated with the poor tumor differentiation [odds ratio (OR) 2.12; 95% CI, 1.45–3.08, P < 0.001)], the propensity toward depth of infiltration (OR 1.69; 95% CI, 1.20–2.39, P = 0.003), and recurrence in patients with CRC (HR, 2.71; 95% CI, 1.31–5.60, P = 0.005). This meta-analysis suggested that a high peripheral blood PLR can be used as a predictor of OS connected with clinicopathological parameters in patients with CRC, not DFS. These ratios may thus contribute to inform more personalized treatment decisions and predict treatment outcomes.
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spelling pubmed-49984462016-09-02 Prognostic role of platelet–lymphocyte ratio in colorectal cancer: A systematic review and meta-analysis Tan, Dewen Fu, Yan Su, Qi Wang, Heling Medicine (Baltimore) 3700 Many studies have been reported that platelet–lymphocyte ratio (PLR) may be associated with the prognosis of colorectal cancer (CRC), but the results are inconsistent. Current opinion on the prognostic role of the PLR in CRC is inconsistent and inconclusive. Therefore, we conduct a meta-analysis that combines these studies and to identify the prognostic value of PLR in patients with CRC. Data were retrieved from PubMed, EMBASE, Cochrane Library, and Web of Science databases that came from inception through January 2016. We extracted data from the characteristics of each study and analyzed the relationship between PLR and overall survival (OS), disease-free survival (DFS), or other prognosis in patients with CRC by using the hazard ratio (HR) and 95% confidence intervals (95% CIs). Of the 256 identified studies, 15 studies were included and a total of 3991 patients were included. In a meta-analysis, patients with an elevated PLR had a significantly lower OS (pooled HR, 1.53; 95% CI, 1.24–1.89; P ≤ 0.001), DFS (pooled HR, 1.68; 95% CI, 1.07–2.62; P = 0.023). Even after sensitivity analyses and trim and fill method, high PLR remains significantly predictive poorer OS, but not DFS. In addition, our meta-analysis indicated that increased PLR is also significantly associated with the poor tumor differentiation [odds ratio (OR) 2.12; 95% CI, 1.45–3.08, P < 0.001)], the propensity toward depth of infiltration (OR 1.69; 95% CI, 1.20–2.39, P = 0.003), and recurrence in patients with CRC (HR, 2.71; 95% CI, 1.31–5.60, P = 0.005). This meta-analysis suggested that a high peripheral blood PLR can be used as a predictor of OS connected with clinicopathological parameters in patients with CRC, not DFS. These ratios may thus contribute to inform more personalized treatment decisions and predict treatment outcomes. Wolters Kluwer Health 2016-06-17 /pmc/articles/PMC4998446/ /pubmed/27310960 http://dx.doi.org/10.1097/MD.0000000000003837 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial, and noncommercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle 3700
Tan, Dewen
Fu, Yan
Su, Qi
Wang, Heling
Prognostic role of platelet–lymphocyte ratio in colorectal cancer: A systematic review and meta-analysis
title Prognostic role of platelet–lymphocyte ratio in colorectal cancer: A systematic review and meta-analysis
title_full Prognostic role of platelet–lymphocyte ratio in colorectal cancer: A systematic review and meta-analysis
title_fullStr Prognostic role of platelet–lymphocyte ratio in colorectal cancer: A systematic review and meta-analysis
title_full_unstemmed Prognostic role of platelet–lymphocyte ratio in colorectal cancer: A systematic review and meta-analysis
title_short Prognostic role of platelet–lymphocyte ratio in colorectal cancer: A systematic review and meta-analysis
title_sort prognostic role of platelet–lymphocyte ratio in colorectal cancer: a systematic review and meta-analysis
topic 3700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998446/
https://www.ncbi.nlm.nih.gov/pubmed/27310960
http://dx.doi.org/10.1097/MD.0000000000003837
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