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Impact of systemic inflammation on gastric cancer outcomes

BACKGROUND: The prognostic value of neutrophil-lymphocyte ratio (NLR) and Glasgow Prognostic Score (GPS) has been extensively validated in various cancers. We aimed to examine the usefulness of a combination of NLR and GPS (named CNG) for predicting survival outcomes in patients after curative resec...

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Autores principales: Liu, Xuechao, Chen, Shangxiang, Liu, Jianjun, Xu, Dazhi, Li, Wei, Zhan, Youqing, Li, Yuanfang, Chen, Yingbo, Zhou, Zhiwei, Sun, Xiaowei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373584/
https://www.ncbi.nlm.nih.gov/pubmed/28358923
http://dx.doi.org/10.1371/journal.pone.0174085
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author Liu, Xuechao
Chen, Shangxiang
Liu, Jianjun
Xu, Dazhi
Li, Wei
Zhan, Youqing
Li, Yuanfang
Chen, Yingbo
Zhou, Zhiwei
Sun, Xiaowei
author_facet Liu, Xuechao
Chen, Shangxiang
Liu, Jianjun
Xu, Dazhi
Li, Wei
Zhan, Youqing
Li, Yuanfang
Chen, Yingbo
Zhou, Zhiwei
Sun, Xiaowei
author_sort Liu, Xuechao
collection PubMed
description BACKGROUND: The prognostic value of neutrophil-lymphocyte ratio (NLR) and Glasgow Prognostic Score (GPS) has been extensively validated in various cancers. We aimed to examine the usefulness of a combination of NLR and GPS (named CNG) for predicting survival outcomes in patients after curative resection for gastric cancer (GC). METHODS: We retrospectively analyzed the records of 1056 patients who underwent curative resection as initial treatment for GC from October 2000 to September 2012. The preoperative CNG was calculated as follows: patients with hypoalbuminemia (< 35 g/L), elevated C-reactive protein (> 10 mg/L), and elevated NLR (≥ 2) were allocated a score of 3; patients with two, one, or no abnormal values were allocated a score of 2, 1, or 0, respectively. RESULTS: The NLR and GPS were the only inflammatory variables independently associated with overall survival (OS) in multivariate analysis. When they were replaced by CNG in multivariate analysis, CNG was independently associated with OS (hazard ratio [HR] for CNG 1 [1.367, 95% CI: 1.065–1.755; P = 0.014], CNG 2 [1.887, 95% CI: 1.182–3.011; P = 0.008], and CNG 3 [2.224, 95% CI: 1.238–3.997; P = 0.008]; P = 0.020). In stage-matched analysis, the prognostic significance was still maintained in stage I-III (P = 0.002, P = 0.042, and P < 0.001, respectively). In addition, 5-year survival rates ranged from 92% (stage I) to 35% (stage III) and from 65%(CNG 0) to 18%(CNG 3) with tumor-nodes-metastasis (TNM) stage or CNG alone. However, the combination of TNM and CNG stratified 5-year survival rates from 98% (TNM I, CNG 0) to 12% (TNM III, CNG 3). CONCLUSION: The preoperative CNG is a novel predictor of postoperative survival, and the combination of CNG and TNM effectively stratifies outcomes in patients after curative resection for GC.
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spelling pubmed-53735842017-04-07 Impact of systemic inflammation on gastric cancer outcomes Liu, Xuechao Chen, Shangxiang Liu, Jianjun Xu, Dazhi Li, Wei Zhan, Youqing Li, Yuanfang Chen, Yingbo Zhou, Zhiwei Sun, Xiaowei PLoS One Research Article BACKGROUND: The prognostic value of neutrophil-lymphocyte ratio (NLR) and Glasgow Prognostic Score (GPS) has been extensively validated in various cancers. We aimed to examine the usefulness of a combination of NLR and GPS (named CNG) for predicting survival outcomes in patients after curative resection for gastric cancer (GC). METHODS: We retrospectively analyzed the records of 1056 patients who underwent curative resection as initial treatment for GC from October 2000 to September 2012. The preoperative CNG was calculated as follows: patients with hypoalbuminemia (< 35 g/L), elevated C-reactive protein (> 10 mg/L), and elevated NLR (≥ 2) were allocated a score of 3; patients with two, one, or no abnormal values were allocated a score of 2, 1, or 0, respectively. RESULTS: The NLR and GPS were the only inflammatory variables independently associated with overall survival (OS) in multivariate analysis. When they were replaced by CNG in multivariate analysis, CNG was independently associated with OS (hazard ratio [HR] for CNG 1 [1.367, 95% CI: 1.065–1.755; P = 0.014], CNG 2 [1.887, 95% CI: 1.182–3.011; P = 0.008], and CNG 3 [2.224, 95% CI: 1.238–3.997; P = 0.008]; P = 0.020). In stage-matched analysis, the prognostic significance was still maintained in stage I-III (P = 0.002, P = 0.042, and P < 0.001, respectively). In addition, 5-year survival rates ranged from 92% (stage I) to 35% (stage III) and from 65%(CNG 0) to 18%(CNG 3) with tumor-nodes-metastasis (TNM) stage or CNG alone. However, the combination of TNM and CNG stratified 5-year survival rates from 98% (TNM I, CNG 0) to 12% (TNM III, CNG 3). CONCLUSION: The preoperative CNG is a novel predictor of postoperative survival, and the combination of CNG and TNM effectively stratifies outcomes in patients after curative resection for GC. Public Library of Science 2017-03-30 /pmc/articles/PMC5373584/ /pubmed/28358923 http://dx.doi.org/10.1371/journal.pone.0174085 Text en © 2017 Liu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Liu, Xuechao
Chen, Shangxiang
Liu, Jianjun
Xu, Dazhi
Li, Wei
Zhan, Youqing
Li, Yuanfang
Chen, Yingbo
Zhou, Zhiwei
Sun, Xiaowei
Impact of systemic inflammation on gastric cancer outcomes
title Impact of systemic inflammation on gastric cancer outcomes
title_full Impact of systemic inflammation on gastric cancer outcomes
title_fullStr Impact of systemic inflammation on gastric cancer outcomes
title_full_unstemmed Impact of systemic inflammation on gastric cancer outcomes
title_short Impact of systemic inflammation on gastric cancer outcomes
title_sort impact of systemic inflammation on gastric cancer outcomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373584/
https://www.ncbi.nlm.nih.gov/pubmed/28358923
http://dx.doi.org/10.1371/journal.pone.0174085
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