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Pretreatment neutrophil-to-lymphocyte ratio as a survival predictor for small-cell lung cancer

BACKGROUND: The inflammatory response indexes, neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR), have prognostic value for a variety of cancers. However, their prognostic value for small-cell lung cancer (SCLC) has been rarely reported. In this study, we monitored changes...

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Autores principales: Wang, Xin, Teng, Feifei, Kong, Li, Yu, Jinming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036593/
https://www.ncbi.nlm.nih.gov/pubmed/27703374
http://dx.doi.org/10.2147/OTT.S106296
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author Wang, Xin
Teng, Feifei
Kong, Li
Yu, Jinming
author_facet Wang, Xin
Teng, Feifei
Kong, Li
Yu, Jinming
author_sort Wang, Xin
collection PubMed
description BACKGROUND: The inflammatory response indexes, neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR), have prognostic value for a variety of cancers. However, their prognostic value for small-cell lung cancer (SCLC) has been rarely reported. In this study, we monitored changes of NLR and PLR along with the clinical outcomes in patients with limited-stage and extensive-stage SCLC who received standard treatments. MATERIALS AND METHODS: We retrospectively reviewed the records of 153 patients who were pathologically diagnosed with SCLC and collected their hematological data at different time points during disease and treatment process. Kaplan–Meier analysis and Cox proportional hazards models were used to determine the prognostic significance of NLR and PLR for overall survival (OS) and progression-free survival (PFS). RESULTS: The median OS and PFS for all patients were 23.3 months and 11.0 months, respectively. After applying cutoffs of 3.2 for NLR and 122.7 for PLR, NLR, but not PLR, showed independent prognostic significance. High-NLR group was associated with shorter median OS (high vs low, 18.0 months vs 31.0 months, P<0.01) and shorter PFS (high vs low, 9.3 months vs 13.0 months, P=0.006). The cumulative 3-year OS rate and 3-year PFS rate of high-NLR group versus low-NLR group were 14.3% versus 37.3% and 8.6% versus 22.9%, respectively. In the multivariate analysis, both disease stage and NLR at diagnosis were independent prognostic factors for OS and PFS. CONCLUSION: The NLR at diagnosis showed significant prognostic value for clinical outcomes in SCLC patients treated with chemoradiotherapy. As an effective biomarker of host immune status, NLR could potentially help monitoring disease progression and adjusting treatment plans.
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spelling pubmed-50365932016-10-04 Pretreatment neutrophil-to-lymphocyte ratio as a survival predictor for small-cell lung cancer Wang, Xin Teng, Feifei Kong, Li Yu, Jinming Onco Targets Ther Original Research BACKGROUND: The inflammatory response indexes, neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR), have prognostic value for a variety of cancers. However, their prognostic value for small-cell lung cancer (SCLC) has been rarely reported. In this study, we monitored changes of NLR and PLR along with the clinical outcomes in patients with limited-stage and extensive-stage SCLC who received standard treatments. MATERIALS AND METHODS: We retrospectively reviewed the records of 153 patients who were pathologically diagnosed with SCLC and collected their hematological data at different time points during disease and treatment process. Kaplan–Meier analysis and Cox proportional hazards models were used to determine the prognostic significance of NLR and PLR for overall survival (OS) and progression-free survival (PFS). RESULTS: The median OS and PFS for all patients were 23.3 months and 11.0 months, respectively. After applying cutoffs of 3.2 for NLR and 122.7 for PLR, NLR, but not PLR, showed independent prognostic significance. High-NLR group was associated with shorter median OS (high vs low, 18.0 months vs 31.0 months, P<0.01) and shorter PFS (high vs low, 9.3 months vs 13.0 months, P=0.006). The cumulative 3-year OS rate and 3-year PFS rate of high-NLR group versus low-NLR group were 14.3% versus 37.3% and 8.6% versus 22.9%, respectively. In the multivariate analysis, both disease stage and NLR at diagnosis were independent prognostic factors for OS and PFS. CONCLUSION: The NLR at diagnosis showed significant prognostic value for clinical outcomes in SCLC patients treated with chemoradiotherapy. As an effective biomarker of host immune status, NLR could potentially help monitoring disease progression and adjusting treatment plans. Dove Medical Press 2016-09-20 /pmc/articles/PMC5036593/ /pubmed/27703374 http://dx.doi.org/10.2147/OTT.S106296 Text en © 2016 Wang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Wang, Xin
Teng, Feifei
Kong, Li
Yu, Jinming
Pretreatment neutrophil-to-lymphocyte ratio as a survival predictor for small-cell lung cancer
title Pretreatment neutrophil-to-lymphocyte ratio as a survival predictor for small-cell lung cancer
title_full Pretreatment neutrophil-to-lymphocyte ratio as a survival predictor for small-cell lung cancer
title_fullStr Pretreatment neutrophil-to-lymphocyte ratio as a survival predictor for small-cell lung cancer
title_full_unstemmed Pretreatment neutrophil-to-lymphocyte ratio as a survival predictor for small-cell lung cancer
title_short Pretreatment neutrophil-to-lymphocyte ratio as a survival predictor for small-cell lung cancer
title_sort pretreatment neutrophil-to-lymphocyte ratio as a survival predictor for small-cell lung cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036593/
https://www.ncbi.nlm.nih.gov/pubmed/27703374
http://dx.doi.org/10.2147/OTT.S106296
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