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Impact of platelet to lymphocyte ratio and metabolic syndrome on the prognosis of colorectal cancer patients

OBJECTIVE: The aim of this study was to evaluate the prognostic value of both platelet to lymphocyte ratio (PLR) and metabolic syndrome (MetS) in colorectal cancer (CRC) patients. PATIENTS AND METHODS: We retrospectively enrolled 1,163 CRC patients. Preoperative values of PLR were stratified into th...

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Autores principales: You, Jie, Zhang, Huxiang, Shen, Yanyan, Chen, Chuanzhi, Liu, Wenyue, Zheng, Minghua, Van Poucke, Sven, Guo, Guilong, Huang, Zonghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403005/
https://www.ncbi.nlm.nih.gov/pubmed/28458563
http://dx.doi.org/10.2147/OTT.S132621
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author You, Jie
Zhang, Huxiang
Shen, Yanyan
Chen, Chuanzhi
Liu, Wenyue
Zheng, Minghua
Van Poucke, Sven
Guo, Guilong
Huang, Zonghai
author_facet You, Jie
Zhang, Huxiang
Shen, Yanyan
Chen, Chuanzhi
Liu, Wenyue
Zheng, Minghua
Van Poucke, Sven
Guo, Guilong
Huang, Zonghai
author_sort You, Jie
collection PubMed
description OBJECTIVE: The aim of this study was to evaluate the prognostic value of both platelet to lymphocyte ratio (PLR) and metabolic syndrome (MetS) in colorectal cancer (CRC) patients. PATIENTS AND METHODS: We retrospectively enrolled 1,163 CRC patients. Preoperative values of PLR were stratified into three groups according to cut-off values of 120 and 220. The Kaplan–Meier analysis was used to calculate cumulative survival rate related to PLR and MetS. Cox proportional hazard regression models were used to analyze potential risk factors and the prognosis associated with PLR and MetS in CRC patients. RESULTS: PLR was significantly higher in the MetS(+) group as compared to MetS(−) group (P=0.039). An elevated PLR was significantly associated with mortality (P=0.014), but not the existence of MetS (P=0.235). In multivariate regression analysis, PLR was an independent risk factor for overall survival (OS) (P=0.046). For the subgroup with a PLR >220, MetS was an independent predictor for both OS and disease-free survival (P=0.039 and P=0.047, respectively) by multivariate analysis adjusting for confounding covariates. In addition, the presence of MetS was associated with a 2-fold increased risk of mortality and tumor recurrences (hazard ratio [HR] =2.0 and HR =1.9, P<0.05, respectively). CONCLUSION: Preoperative PLR was associated with MetS in CRC patients. Testing for the combined presence of PLR and MetS could potentially improve the predictive accuracy of CRC prognosis.
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spelling pubmed-54030052017-04-28 Impact of platelet to lymphocyte ratio and metabolic syndrome on the prognosis of colorectal cancer patients You, Jie Zhang, Huxiang Shen, Yanyan Chen, Chuanzhi Liu, Wenyue Zheng, Minghua Van Poucke, Sven Guo, Guilong Huang, Zonghai Onco Targets Ther Original Research OBJECTIVE: The aim of this study was to evaluate the prognostic value of both platelet to lymphocyte ratio (PLR) and metabolic syndrome (MetS) in colorectal cancer (CRC) patients. PATIENTS AND METHODS: We retrospectively enrolled 1,163 CRC patients. Preoperative values of PLR were stratified into three groups according to cut-off values of 120 and 220. The Kaplan–Meier analysis was used to calculate cumulative survival rate related to PLR and MetS. Cox proportional hazard regression models were used to analyze potential risk factors and the prognosis associated with PLR and MetS in CRC patients. RESULTS: PLR was significantly higher in the MetS(+) group as compared to MetS(−) group (P=0.039). An elevated PLR was significantly associated with mortality (P=0.014), but not the existence of MetS (P=0.235). In multivariate regression analysis, PLR was an independent risk factor for overall survival (OS) (P=0.046). For the subgroup with a PLR >220, MetS was an independent predictor for both OS and disease-free survival (P=0.039 and P=0.047, respectively) by multivariate analysis adjusting for confounding covariates. In addition, the presence of MetS was associated with a 2-fold increased risk of mortality and tumor recurrences (hazard ratio [HR] =2.0 and HR =1.9, P<0.05, respectively). CONCLUSION: Preoperative PLR was associated with MetS in CRC patients. Testing for the combined presence of PLR and MetS could potentially improve the predictive accuracy of CRC prognosis. Dove Medical Press 2017-04-18 /pmc/articles/PMC5403005/ /pubmed/28458563 http://dx.doi.org/10.2147/OTT.S132621 Text en © 2017 You 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
You, Jie
Zhang, Huxiang
Shen, Yanyan
Chen, Chuanzhi
Liu, Wenyue
Zheng, Minghua
Van Poucke, Sven
Guo, Guilong
Huang, Zonghai
Impact of platelet to lymphocyte ratio and metabolic syndrome on the prognosis of colorectal cancer patients
title Impact of platelet to lymphocyte ratio and metabolic syndrome on the prognosis of colorectal cancer patients
title_full Impact of platelet to lymphocyte ratio and metabolic syndrome on the prognosis of colorectal cancer patients
title_fullStr Impact of platelet to lymphocyte ratio and metabolic syndrome on the prognosis of colorectal cancer patients
title_full_unstemmed Impact of platelet to lymphocyte ratio and metabolic syndrome on the prognosis of colorectal cancer patients
title_short Impact of platelet to lymphocyte ratio and metabolic syndrome on the prognosis of colorectal cancer patients
title_sort impact of platelet to lymphocyte ratio and metabolic syndrome on the prognosis of colorectal cancer patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403005/
https://www.ncbi.nlm.nih.gov/pubmed/28458563
http://dx.doi.org/10.2147/OTT.S132621
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