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Prognostic values of hematological biomarkers in nasopharyngeal carcinoma patients treated with intensity-modulated radiotherapy

PURPOSE: In this study, we evaluated the prognostic values of hematological biomarkers in primary nasopharyngeal carcinoma (NPC) patients receiving definitive intensity-modulated radiotherapy (IMRT). METHODS: There were 427 NPC patients enrolled between January 2010 and March 2013 at Fudan Universit...

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Autores principales: Ye, Lulu, Oei, Ronald Wihal, Kong, Fangfang, Xu, Tingting, Shen, Chunying, Wang, Xiaoshen, He, Xiayun, Kong, Lin, Hu, Chaosu, Ying, Hongmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893672/
https://www.ncbi.nlm.nih.gov/pubmed/29589142
http://dx.doi.org/10.1007/s00405-018-4956-x
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author Ye, Lulu
Oei, Ronald Wihal
Kong, Fangfang
Xu, Tingting
Shen, Chunying
Wang, Xiaoshen
He, Xiayun
Kong, Lin
Hu, Chaosu
Ying, Hongmei
author_facet Ye, Lulu
Oei, Ronald Wihal
Kong, Fangfang
Xu, Tingting
Shen, Chunying
Wang, Xiaoshen
He, Xiayun
Kong, Lin
Hu, Chaosu
Ying, Hongmei
author_sort Ye, Lulu
collection PubMed
description PURPOSE: In this study, we evaluated the prognostic values of hematological biomarkers in primary nasopharyngeal carcinoma (NPC) patients receiving definitive intensity-modulated radiotherapy (IMRT). METHODS: There were 427 NPC patients enrolled between January 2010 and March 2013 at Fudan University Shanghai Cancer Center. Pre-treatment absolute neutrophil count (ANC), platelet count (APC), lymphocyte count (ALC), neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) were collected as prognostic biomarkers. The Kaplan–Meier method and log-rank test were utilized to calculate progression-free survival (PFS) and overall survival (OS). The Cox proportional hazard models were applied to assess variables. RESULTS: ANC, APC and ALC were declined, while NLR and PLR were elevated significantly after therapy (P < 0.001 each). On multivariate analysis, pre-treatment NLR ≥ 2.32 was associated with shortened OS (P = 0.048) and PFS (P = 0.008), whereas PLR ≥ 123.0 was related with inferior OS (P = 0.032), yet it was not correlated with PFS (P = 0.161). CONCLUSIONS: High pre-treatment NLR and PLR indicated poor survival in NPC patients treated with IMRT-based therapy. As easily accessible and economically feasible biomarkers, NLR and PLR can be applied into clinical practice, in combination with current TNM staging, to design a more personalized treatment in these patients.
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spelling pubmed-58936722018-04-16 Prognostic values of hematological biomarkers in nasopharyngeal carcinoma patients treated with intensity-modulated radiotherapy Ye, Lulu Oei, Ronald Wihal Kong, Fangfang Xu, Tingting Shen, Chunying Wang, Xiaoshen He, Xiayun Kong, Lin Hu, Chaosu Ying, Hongmei Eur Arch Otorhinolaryngol Head and Neck PURPOSE: In this study, we evaluated the prognostic values of hematological biomarkers in primary nasopharyngeal carcinoma (NPC) patients receiving definitive intensity-modulated radiotherapy (IMRT). METHODS: There were 427 NPC patients enrolled between January 2010 and March 2013 at Fudan University Shanghai Cancer Center. Pre-treatment absolute neutrophil count (ANC), platelet count (APC), lymphocyte count (ALC), neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) were collected as prognostic biomarkers. The Kaplan–Meier method and log-rank test were utilized to calculate progression-free survival (PFS) and overall survival (OS). The Cox proportional hazard models were applied to assess variables. RESULTS: ANC, APC and ALC were declined, while NLR and PLR were elevated significantly after therapy (P < 0.001 each). On multivariate analysis, pre-treatment NLR ≥ 2.32 was associated with shortened OS (P = 0.048) and PFS (P = 0.008), whereas PLR ≥ 123.0 was related with inferior OS (P = 0.032), yet it was not correlated with PFS (P = 0.161). CONCLUSIONS: High pre-treatment NLR and PLR indicated poor survival in NPC patients treated with IMRT-based therapy. As easily accessible and economically feasible biomarkers, NLR and PLR can be applied into clinical practice, in combination with current TNM staging, to design a more personalized treatment in these patients. Springer Berlin Heidelberg 2018-03-27 2018 /pmc/articles/PMC5893672/ /pubmed/29589142 http://dx.doi.org/10.1007/s00405-018-4956-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Head and Neck
Ye, Lulu
Oei, Ronald Wihal
Kong, Fangfang
Xu, Tingting
Shen, Chunying
Wang, Xiaoshen
He, Xiayun
Kong, Lin
Hu, Chaosu
Ying, Hongmei
Prognostic values of hematological biomarkers in nasopharyngeal carcinoma patients treated with intensity-modulated radiotherapy
title Prognostic values of hematological biomarkers in nasopharyngeal carcinoma patients treated with intensity-modulated radiotherapy
title_full Prognostic values of hematological biomarkers in nasopharyngeal carcinoma patients treated with intensity-modulated radiotherapy
title_fullStr Prognostic values of hematological biomarkers in nasopharyngeal carcinoma patients treated with intensity-modulated radiotherapy
title_full_unstemmed Prognostic values of hematological biomarkers in nasopharyngeal carcinoma patients treated with intensity-modulated radiotherapy
title_short Prognostic values of hematological biomarkers in nasopharyngeal carcinoma patients treated with intensity-modulated radiotherapy
title_sort prognostic values of hematological biomarkers in nasopharyngeal carcinoma patients treated with intensity-modulated radiotherapy
topic Head and Neck
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893672/
https://www.ncbi.nlm.nih.gov/pubmed/29589142
http://dx.doi.org/10.1007/s00405-018-4956-x
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