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Neutrophils: driving progression and poor prognosis in hepatocellular carcinoma?

BACKGROUND: Irrespective of the underlying aetiology, 90% of hepatocellular carcinomas arise and progress on a background of chronic inflammation. We have explored the independent prognostic value of circulating inflammatory cells. METHODS: Peripheral blood count data sets from 583 consecutive patie...

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Autores principales: Margetts, Jane, Ogle, Laura F, Chan, Stephen L, Chan, Anthony W H, Chan, K C Allen, Jamieson, David, Willoughby, Catherine E, Mann, Derek A, Wilson, Caroline L, Manas, Derek M, Yeo, Winnie, Reeves, Helen L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785742/
https://www.ncbi.nlm.nih.gov/pubmed/29123264
http://dx.doi.org/10.1038/bjc.2017.386
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author Margetts, Jane
Ogle, Laura F
Chan, Stephen L
Chan, Anthony W H
Chan, K C Allen
Jamieson, David
Willoughby, Catherine E
Mann, Derek A
Wilson, Caroline L
Manas, Derek M
Yeo, Winnie
Reeves, Helen L
author_facet Margetts, Jane
Ogle, Laura F
Chan, Stephen L
Chan, Anthony W H
Chan, K C Allen
Jamieson, David
Willoughby, Catherine E
Mann, Derek A
Wilson, Caroline L
Manas, Derek M
Yeo, Winnie
Reeves, Helen L
author_sort Margetts, Jane
collection PubMed
description BACKGROUND: Irrespective of the underlying aetiology, 90% of hepatocellular carcinomas arise and progress on a background of chronic inflammation. We have explored the independent prognostic value of circulating inflammatory cells. METHODS: Peripheral blood count data sets from 583 consecutive patients presenting to a single UK centre (2000–2010) were analysed for associations with tumour stage, liver function, performance status (PST) and survival. Validation was in an independent Hong Kong cohort (585 patients; 2007–2013). RESULTS: In both UK and Hong Kong cohorts, neutrophils, platelets, lymphocytes, the neutrophil/lymphocyte ratio (NLR) and the Systemic Immune-Inflammation Index (SII) correlated stepwise, either increasing or decreasing (lymphocytes), with tumour node metastasis (TNM) and Childs–Pugh stage, PST and consequently with the combined Barcelona Clinic for Liver Cancer stage. Survival analyses confirmed the NLR and SII as highly significant prognostic biomarkers. Focused on individual cell types, only the neutrophil count was independently associated with both TNM stage and PST, as well as being significantly and independently associated with poorer survival. CONCLUSIONS: In this study of 1168 patients, neutrophils alone, rather than lymphocytes or platelets, were independently associated with outcome. These data support further characterisation of a potentially distinctive role for neutrophils as facilitators of tumour progression and deteriorating performance.
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spelling pubmed-57857422019-01-01 Neutrophils: driving progression and poor prognosis in hepatocellular carcinoma? Margetts, Jane Ogle, Laura F Chan, Stephen L Chan, Anthony W H Chan, K C Allen Jamieson, David Willoughby, Catherine E Mann, Derek A Wilson, Caroline L Manas, Derek M Yeo, Winnie Reeves, Helen L Br J Cancer Molecular Diagnostics BACKGROUND: Irrespective of the underlying aetiology, 90% of hepatocellular carcinomas arise and progress on a background of chronic inflammation. We have explored the independent prognostic value of circulating inflammatory cells. METHODS: Peripheral blood count data sets from 583 consecutive patients presenting to a single UK centre (2000–2010) were analysed for associations with tumour stage, liver function, performance status (PST) and survival. Validation was in an independent Hong Kong cohort (585 patients; 2007–2013). RESULTS: In both UK and Hong Kong cohorts, neutrophils, platelets, lymphocytes, the neutrophil/lymphocyte ratio (NLR) and the Systemic Immune-Inflammation Index (SII) correlated stepwise, either increasing or decreasing (lymphocytes), with tumour node metastasis (TNM) and Childs–Pugh stage, PST and consequently with the combined Barcelona Clinic for Liver Cancer stage. Survival analyses confirmed the NLR and SII as highly significant prognostic biomarkers. Focused on individual cell types, only the neutrophil count was independently associated with both TNM stage and PST, as well as being significantly and independently associated with poorer survival. CONCLUSIONS: In this study of 1168 patients, neutrophils alone, rather than lymphocytes or platelets, were independently associated with outcome. These data support further characterisation of a potentially distinctive role for neutrophils as facilitators of tumour progression and deteriorating performance. Nature Publishing Group 2018-01 2017-11-09 /pmc/articles/PMC5785742/ /pubmed/29123264 http://dx.doi.org/10.1038/bjc.2017.386 Text en Copyright © 2018 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Molecular Diagnostics
Margetts, Jane
Ogle, Laura F
Chan, Stephen L
Chan, Anthony W H
Chan, K C Allen
Jamieson, David
Willoughby, Catherine E
Mann, Derek A
Wilson, Caroline L
Manas, Derek M
Yeo, Winnie
Reeves, Helen L
Neutrophils: driving progression and poor prognosis in hepatocellular carcinoma?
title Neutrophils: driving progression and poor prognosis in hepatocellular carcinoma?
title_full Neutrophils: driving progression and poor prognosis in hepatocellular carcinoma?
title_fullStr Neutrophils: driving progression and poor prognosis in hepatocellular carcinoma?
title_full_unstemmed Neutrophils: driving progression and poor prognosis in hepatocellular carcinoma?
title_short Neutrophils: driving progression and poor prognosis in hepatocellular carcinoma?
title_sort neutrophils: driving progression and poor prognosis in hepatocellular carcinoma?
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785742/
https://www.ncbi.nlm.nih.gov/pubmed/29123264
http://dx.doi.org/10.1038/bjc.2017.386
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