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Inflammatory markers in intrahepatic cholangiocarcinoma: Effects of advanced liver disease
BACKGROUND: To investigate the neutrophil‐to‐lymphocyte ratio (NLR), platelet‐to‐lymphocyte ratio (PLR), and systemic immune‐inflammation index (SII) as prognostic biomarkers in intrahepatic cholangiocarcinoma (ICC) with a focus on viral hepatitis and liver status. METHODS: In this retrospective coh...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792510/ https://www.ncbi.nlm.nih.gov/pubmed/31429524 http://dx.doi.org/10.1002/cam4.2373 |
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author | Sellers, Cortlandt M. Uhlig, Johannes Ludwig, Johannes M. Stein, Stacey M. Kim, Hyun S. |
author_facet | Sellers, Cortlandt M. Uhlig, Johannes Ludwig, Johannes M. Stein, Stacey M. Kim, Hyun S. |
author_sort | Sellers, Cortlandt M. |
collection | PubMed |
description | BACKGROUND: To investigate the neutrophil‐to‐lymphocyte ratio (NLR), platelet‐to‐lymphocyte ratio (PLR), and systemic immune‐inflammation index (SII) as prognostic biomarkers in intrahepatic cholangiocarcinoma (ICC) with a focus on viral hepatitis and liver status. METHODS: In this retrospective cohort study, patients from the institutional cancer registry with ICC from 2005 to 2016 were stratified by treatment group. Baseline inflammatory markers were dichotomized at the median. Overall survival (OS) was assessed via Kaplan‐Meier curves and Cox proportional hazard models. Multiple patient, liver, and tumor factors were included in the multivariable analysis (MVA). RESULTS: About 131 patients (median age 65 years, 52% male, 76% Caucasian) had a median OS of 13.0 months. Resection/interventional oncology with/without systemic therapy had improved survival vs systemic therapy alone in Child‐Pugh A patients (P < 0.01). In Child‐Pugh B/C patients, this survival difference became nonsignificant (P = 0.22). Increased NLR and SII were associated with decreased survival (P < 0.01), while dichotomized PLR was not (P = 0.3). On MVA, increased NLR remained an independent prognostic factor (HR 1.6, P < 0.05). In Child‐Pugh class A (n = 94), low‐NLR had higher OS vs high‐NLR (25.4 vs 12.2 months, P < 0.01). In Child‐Pugh class B/C (n = 28), NLR did not have a significant effect on median OS (low‐ vs high‐NLR: 6.7 vs 2.9 months, P = 0.2). Child‐Pugh class acted as an effect modifier on MVA for NLR (P = 0.0124). CONCLUSIONS: The NLR has a stronger impact as a prognostic marker in ICC over the PLR and SII. This survival effect is decreased in advanced liver disease. |
format | Online Article Text |
id | pubmed-6792510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67925102019-10-21 Inflammatory markers in intrahepatic cholangiocarcinoma: Effects of advanced liver disease Sellers, Cortlandt M. Uhlig, Johannes Ludwig, Johannes M. Stein, Stacey M. Kim, Hyun S. Cancer Med Clinical Cancer Research BACKGROUND: To investigate the neutrophil‐to‐lymphocyte ratio (NLR), platelet‐to‐lymphocyte ratio (PLR), and systemic immune‐inflammation index (SII) as prognostic biomarkers in intrahepatic cholangiocarcinoma (ICC) with a focus on viral hepatitis and liver status. METHODS: In this retrospective cohort study, patients from the institutional cancer registry with ICC from 2005 to 2016 were stratified by treatment group. Baseline inflammatory markers were dichotomized at the median. Overall survival (OS) was assessed via Kaplan‐Meier curves and Cox proportional hazard models. Multiple patient, liver, and tumor factors were included in the multivariable analysis (MVA). RESULTS: About 131 patients (median age 65 years, 52% male, 76% Caucasian) had a median OS of 13.0 months. Resection/interventional oncology with/without systemic therapy had improved survival vs systemic therapy alone in Child‐Pugh A patients (P < 0.01). In Child‐Pugh B/C patients, this survival difference became nonsignificant (P = 0.22). Increased NLR and SII were associated with decreased survival (P < 0.01), while dichotomized PLR was not (P = 0.3). On MVA, increased NLR remained an independent prognostic factor (HR 1.6, P < 0.05). In Child‐Pugh class A (n = 94), low‐NLR had higher OS vs high‐NLR (25.4 vs 12.2 months, P < 0.01). In Child‐Pugh class B/C (n = 28), NLR did not have a significant effect on median OS (low‐ vs high‐NLR: 6.7 vs 2.9 months, P = 0.2). Child‐Pugh class acted as an effect modifier on MVA for NLR (P = 0.0124). CONCLUSIONS: The NLR has a stronger impact as a prognostic marker in ICC over the PLR and SII. This survival effect is decreased in advanced liver disease. John Wiley and Sons Inc. 2019-08-20 /pmc/articles/PMC6792510/ /pubmed/31429524 http://dx.doi.org/10.1002/cam4.2373 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the 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 | Clinical Cancer Research Sellers, Cortlandt M. Uhlig, Johannes Ludwig, Johannes M. Stein, Stacey M. Kim, Hyun S. Inflammatory markers in intrahepatic cholangiocarcinoma: Effects of advanced liver disease |
title | Inflammatory markers in intrahepatic cholangiocarcinoma: Effects of advanced liver disease |
title_full | Inflammatory markers in intrahepatic cholangiocarcinoma: Effects of advanced liver disease |
title_fullStr | Inflammatory markers in intrahepatic cholangiocarcinoma: Effects of advanced liver disease |
title_full_unstemmed | Inflammatory markers in intrahepatic cholangiocarcinoma: Effects of advanced liver disease |
title_short | Inflammatory markers in intrahepatic cholangiocarcinoma: Effects of advanced liver disease |
title_sort | inflammatory markers in intrahepatic cholangiocarcinoma: effects of advanced liver disease |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792510/ https://www.ncbi.nlm.nih.gov/pubmed/31429524 http://dx.doi.org/10.1002/cam4.2373 |
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