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Platelet‐to‐lymphocyte ratio could be a promising prognostic biomarker for survival of colorectal cancer: a systematic review and meta‐analysis
Inflammation is one of the most important causes leading to colorectal carcinogenesis, and inflammatory biomarkers such as the platelet‐to‐lymphocyte ratio (PLR) might predict survival in colorectal cancer (CRC). However, the prognostic value of PLR in CRC patients remains controversial. The prognos...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932454/ https://www.ncbi.nlm.nih.gov/pubmed/27398314 http://dx.doi.org/10.1002/2211-5463.12083 |
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author | Peng, Hong‐Xin Lin, Kang He, Bang‐Shun Pan, Yu‐Qin Ying, Hou‐Qun Hu, Xiu‐Xiu Xu, Tao Wang, Shu‐Kui |
author_facet | Peng, Hong‐Xin Lin, Kang He, Bang‐Shun Pan, Yu‐Qin Ying, Hou‐Qun Hu, Xiu‐Xiu Xu, Tao Wang, Shu‐Kui |
author_sort | Peng, Hong‐Xin |
collection | PubMed |
description | Inflammation is one of the most important causes leading to colorectal carcinogenesis, and inflammatory biomarkers such as the platelet‐to‐lymphocyte ratio (PLR) might predict survival in colorectal cancer (CRC). However, the prognostic value of PLR in CRC patients remains controversial. The prognostic value of PLR was comprehensively analyzed in 12 articles including 3541 CRC patients (10 for overall survival (OS), seven for disease‐free survival (DFS), three for recurrence‐free survival (RFS), and three for cancer‐specific survival (CSS)) in this study. The overall pooled hazard ratios (HRs) of PLR for OS, DFS, and CSS were significant at 1.29 (95% confidence interval, CI = 1.13–1.47, P(H) = 0.149), 1.43 (95% CI = 1.03–1.97, P(H) = 0.025), and 1.26 (95% CI = 1.04–1.52, P(H) = 0.223), respectively. However, there was no evidence of significance for RFS (HR = 1.29, 95% CI = 0.98–1.70, P(H) = 0.231) in our study. Stratified analyses indicated elevated PLR was a predictor of poor OS (metastatic patients) and DFS (Caucasian population) and was also significantly associated with OS in univariate analysis (HR = 1.35, 95% CI = 1.14–1.60, P(H) = 0.532) and those only treated surgically (HR = 1.37, 95% CI = 1.10–1.70, P(H) = 1.080). However, our findings indicated that elevated PLR is a promising prognostic biomarker for colorectal cancer, especially in metastatic Caucasian CRC patients. |
format | Online Article Text |
id | pubmed-4932454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49324542016-07-08 Platelet‐to‐lymphocyte ratio could be a promising prognostic biomarker for survival of colorectal cancer: a systematic review and meta‐analysis Peng, Hong‐Xin Lin, Kang He, Bang‐Shun Pan, Yu‐Qin Ying, Hou‐Qun Hu, Xiu‐Xiu Xu, Tao Wang, Shu‐Kui FEBS Open Bio Research Articles Inflammation is one of the most important causes leading to colorectal carcinogenesis, and inflammatory biomarkers such as the platelet‐to‐lymphocyte ratio (PLR) might predict survival in colorectal cancer (CRC). However, the prognostic value of PLR in CRC patients remains controversial. The prognostic value of PLR was comprehensively analyzed in 12 articles including 3541 CRC patients (10 for overall survival (OS), seven for disease‐free survival (DFS), three for recurrence‐free survival (RFS), and three for cancer‐specific survival (CSS)) in this study. The overall pooled hazard ratios (HRs) of PLR for OS, DFS, and CSS were significant at 1.29 (95% confidence interval, CI = 1.13–1.47, P(H) = 0.149), 1.43 (95% CI = 1.03–1.97, P(H) = 0.025), and 1.26 (95% CI = 1.04–1.52, P(H) = 0.223), respectively. However, there was no evidence of significance for RFS (HR = 1.29, 95% CI = 0.98–1.70, P(H) = 0.231) in our study. Stratified analyses indicated elevated PLR was a predictor of poor OS (metastatic patients) and DFS (Caucasian population) and was also significantly associated with OS in univariate analysis (HR = 1.35, 95% CI = 1.14–1.60, P(H) = 0.532) and those only treated surgically (HR = 1.37, 95% CI = 1.10–1.70, P(H) = 1.080). However, our findings indicated that elevated PLR is a promising prognostic biomarker for colorectal cancer, especially in metastatic Caucasian CRC patients. John Wiley and Sons Inc. 2016-06-16 /pmc/articles/PMC4932454/ /pubmed/27398314 http://dx.doi.org/10.1002/2211-5463.12083 Text en © 2016 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Peng, Hong‐Xin Lin, Kang He, Bang‐Shun Pan, Yu‐Qin Ying, Hou‐Qun Hu, Xiu‐Xiu Xu, Tao Wang, Shu‐Kui Platelet‐to‐lymphocyte ratio could be a promising prognostic biomarker for survival of colorectal cancer: a systematic review and meta‐analysis |
title | Platelet‐to‐lymphocyte ratio could be a promising prognostic biomarker for survival of colorectal cancer: a systematic review and meta‐analysis |
title_full | Platelet‐to‐lymphocyte ratio could be a promising prognostic biomarker for survival of colorectal cancer: a systematic review and meta‐analysis |
title_fullStr | Platelet‐to‐lymphocyte ratio could be a promising prognostic biomarker for survival of colorectal cancer: a systematic review and meta‐analysis |
title_full_unstemmed | Platelet‐to‐lymphocyte ratio could be a promising prognostic biomarker for survival of colorectal cancer: a systematic review and meta‐analysis |
title_short | Platelet‐to‐lymphocyte ratio could be a promising prognostic biomarker for survival of colorectal cancer: a systematic review and meta‐analysis |
title_sort | platelet‐to‐lymphocyte ratio could be a promising prognostic biomarker for survival of colorectal cancer: a systematic review and meta‐analysis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932454/ https://www.ncbi.nlm.nih.gov/pubmed/27398314 http://dx.doi.org/10.1002/2211-5463.12083 |
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