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Prognostic performance of inflammation-based prognostic indices in primary operable non-small cell lung cancer

BACKGROUND: At least 30% of patients with primary resectable non-small cell lung cancer (NSCLC) will experience a relapse in their disease within 5 years following definitive treatment. Clinicopathological predictors have proved to be suboptimal in identifying high-risk patients. We aimed to establi...

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Autores principales: Pinato, D J, Shiner, R J, Seckl, M J, Stebbing, J, Sharma, R, Mauri, F A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992503/
https://www.ncbi.nlm.nih.gov/pubmed/24667648
http://dx.doi.org/10.1038/bjc.2014.145
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author Pinato, D J
Shiner, R J
Seckl, M J
Stebbing, J
Sharma, R
Mauri, F A
author_facet Pinato, D J
Shiner, R J
Seckl, M J
Stebbing, J
Sharma, R
Mauri, F A
author_sort Pinato, D J
collection PubMed
description BACKGROUND: At least 30% of patients with primary resectable non-small cell lung cancer (NSCLC) will experience a relapse in their disease within 5 years following definitive treatment. Clinicopathological predictors have proved to be suboptimal in identifying high-risk patients. We aimed to establish whether inflammation-based scores offer an improved prognostic ability in terms of estimating overall (OS) and recurrence-free survival (RFS) in a cohort of operable, early-stage NSCLC patients. METHODS: Clinicopathological, demographic and treatment data were collected prospectively for 220 patients operated for primary NSCLC at the Hammersmith Hospital from 2004 to 2011. Pretreatment modified Glasgow Prognostic Score (mGPS), neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) were tested together with established prognostic factors in uni- and multivariate Cox regression analyses of OS and RFS. RESULTS: Half of the patients were male, with a median age of 65. A total of 57% were classified as stage I with adenocarcinoma being the most prevalent subtype (60%). Univariate analyses of survival revealed stage (P<0.001), grade (P=0.02), lymphovascular (LVI, P=0.001), visceral pleural invasion (VPI, P=0.003), mGPS (P=0.02) and NLR (P=0.04) as predictors of OS, with stage (P<0.001), VPI (P=0.02) and NLR (P=0.002) being confirmed as independent prognostic factors on multivariate analyses. Patients with more advanced stage (P<0.001) and LVI (P=0.008) had significantly shorter RFS. CONCLUSIONS: An elevated NLR identifies operable NSCLC patients with a poor prognostic outlook and an OS difference of almost 2 years compared to those with a normal score at diagnosis. Our study validates the clinical utility of the NLR in early-stage NSCLC.
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spelling pubmed-39925032015-04-15 Prognostic performance of inflammation-based prognostic indices in primary operable non-small cell lung cancer Pinato, D J Shiner, R J Seckl, M J Stebbing, J Sharma, R Mauri, F A Br J Cancer Clinical Study BACKGROUND: At least 30% of patients with primary resectable non-small cell lung cancer (NSCLC) will experience a relapse in their disease within 5 years following definitive treatment. Clinicopathological predictors have proved to be suboptimal in identifying high-risk patients. We aimed to establish whether inflammation-based scores offer an improved prognostic ability in terms of estimating overall (OS) and recurrence-free survival (RFS) in a cohort of operable, early-stage NSCLC patients. METHODS: Clinicopathological, demographic and treatment data were collected prospectively for 220 patients operated for primary NSCLC at the Hammersmith Hospital from 2004 to 2011. Pretreatment modified Glasgow Prognostic Score (mGPS), neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) were tested together with established prognostic factors in uni- and multivariate Cox regression analyses of OS and RFS. RESULTS: Half of the patients were male, with a median age of 65. A total of 57% were classified as stage I with adenocarcinoma being the most prevalent subtype (60%). Univariate analyses of survival revealed stage (P<0.001), grade (P=0.02), lymphovascular (LVI, P=0.001), visceral pleural invasion (VPI, P=0.003), mGPS (P=0.02) and NLR (P=0.04) as predictors of OS, with stage (P<0.001), VPI (P=0.02) and NLR (P=0.002) being confirmed as independent prognostic factors on multivariate analyses. Patients with more advanced stage (P<0.001) and LVI (P=0.008) had significantly shorter RFS. CONCLUSIONS: An elevated NLR identifies operable NSCLC patients with a poor prognostic outlook and an OS difference of almost 2 years compared to those with a normal score at diagnosis. Our study validates the clinical utility of the NLR in early-stage NSCLC. Nature Publishing Group 2014-04-15 2014-03-25 /pmc/articles/PMC3992503/ /pubmed/24667648 http://dx.doi.org/10.1038/bjc.2014.145 Text en Copyright © 2014 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Clinical Study
Pinato, D J
Shiner, R J
Seckl, M J
Stebbing, J
Sharma, R
Mauri, F A
Prognostic performance of inflammation-based prognostic indices in primary operable non-small cell lung cancer
title Prognostic performance of inflammation-based prognostic indices in primary operable non-small cell lung cancer
title_full Prognostic performance of inflammation-based prognostic indices in primary operable non-small cell lung cancer
title_fullStr Prognostic performance of inflammation-based prognostic indices in primary operable non-small cell lung cancer
title_full_unstemmed Prognostic performance of inflammation-based prognostic indices in primary operable non-small cell lung cancer
title_short Prognostic performance of inflammation-based prognostic indices in primary operable non-small cell lung cancer
title_sort prognostic performance of inflammation-based prognostic indices in primary operable non-small cell lung cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992503/
https://www.ncbi.nlm.nih.gov/pubmed/24667648
http://dx.doi.org/10.1038/bjc.2014.145
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