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Utility of red cell distribution width as a diagnostic and prognostic marker in non-small cell lung cancer

An increasing number of studies have indicated that red blood cell distribution width (RDW) may be a novel biomarker for the diagnosis and prognosis of various malignancies. However, to date, data on the association of RDW with non-small cell lung cancer (NSCLC) are unclear. Our present study aimed...

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Autores principales: Song, Bin, Shi, Pengchong, Xiao, Jianhong, Song, Yanfang, Zeng, Menglu, Cao, Yingping, Zhu, Xianjin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7515922/
https://www.ncbi.nlm.nih.gov/pubmed/32973271
http://dx.doi.org/10.1038/s41598-020-72585-4
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author Song, Bin
Shi, Pengchong
Xiao, Jianhong
Song, Yanfang
Zeng, Menglu
Cao, Yingping
Zhu, Xianjin
author_facet Song, Bin
Shi, Pengchong
Xiao, Jianhong
Song, Yanfang
Zeng, Menglu
Cao, Yingping
Zhu, Xianjin
author_sort Song, Bin
collection PubMed
description An increasing number of studies have indicated that red blood cell distribution width (RDW) may be a novel biomarker for the diagnosis and prognosis of various malignancies. However, to date, data on the association of RDW with non-small cell lung cancer (NSCLC) are unclear. Our present study aimed to explore the value of RDW in NSCLC patients. A total of 338 NSCLC patients, 109 small cell lung cancer (SCLC) patients, and 302 healthy participants were retrospectively analyzed between January 2016 and December 2018. In the present study, we found that RDW was significantly increased in NSCLC patients. Receiver-operating characteristic (ROC) analysis showed that the area under the ROC curve (AUC) of RDW was 0.753 in discriminating NSCLC patients from healthy participants, the optimal cut-off value of RDW was 12.95, and the specificity and sensitivity were 76.33% and 76.16%, respectively. Further analysis found that RDW can enhance the diagnostic performance of Cyfra21-1 and NSE in discriminating NSCLC patients from healthy participants or SCLC patients. Among NSCLC patients, RDW was significantly correlated with TNM stage, T stage, N stage, M stage, and Cyfra21-1, indicating that RDW may be helpful for predicting the prognosis of NSCLC patients. Our findings suggest that RDW can be used as an auxiliary marker for the diagnosis and prognosis of NSCLC.
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spelling pubmed-75159222020-09-29 Utility of red cell distribution width as a diagnostic and prognostic marker in non-small cell lung cancer Song, Bin Shi, Pengchong Xiao, Jianhong Song, Yanfang Zeng, Menglu Cao, Yingping Zhu, Xianjin Sci Rep Article An increasing number of studies have indicated that red blood cell distribution width (RDW) may be a novel biomarker for the diagnosis and prognosis of various malignancies. However, to date, data on the association of RDW with non-small cell lung cancer (NSCLC) are unclear. Our present study aimed to explore the value of RDW in NSCLC patients. A total of 338 NSCLC patients, 109 small cell lung cancer (SCLC) patients, and 302 healthy participants were retrospectively analyzed between January 2016 and December 2018. In the present study, we found that RDW was significantly increased in NSCLC patients. Receiver-operating characteristic (ROC) analysis showed that the area under the ROC curve (AUC) of RDW was 0.753 in discriminating NSCLC patients from healthy participants, the optimal cut-off value of RDW was 12.95, and the specificity and sensitivity were 76.33% and 76.16%, respectively. Further analysis found that RDW can enhance the diagnostic performance of Cyfra21-1 and NSE in discriminating NSCLC patients from healthy participants or SCLC patients. Among NSCLC patients, RDW was significantly correlated with TNM stage, T stage, N stage, M stage, and Cyfra21-1, indicating that RDW may be helpful for predicting the prognosis of NSCLC patients. Our findings suggest that RDW can be used as an auxiliary marker for the diagnosis and prognosis of NSCLC. Nature Publishing Group UK 2020-09-24 /pmc/articles/PMC7515922/ /pubmed/32973271 http://dx.doi.org/10.1038/s41598-020-72585-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Song, Bin
Shi, Pengchong
Xiao, Jianhong
Song, Yanfang
Zeng, Menglu
Cao, Yingping
Zhu, Xianjin
Utility of red cell distribution width as a diagnostic and prognostic marker in non-small cell lung cancer
title Utility of red cell distribution width as a diagnostic and prognostic marker in non-small cell lung cancer
title_full Utility of red cell distribution width as a diagnostic and prognostic marker in non-small cell lung cancer
title_fullStr Utility of red cell distribution width as a diagnostic and prognostic marker in non-small cell lung cancer
title_full_unstemmed Utility of red cell distribution width as a diagnostic and prognostic marker in non-small cell lung cancer
title_short Utility of red cell distribution width as a diagnostic and prognostic marker in non-small cell lung cancer
title_sort utility of red cell distribution width as a diagnostic and prognostic marker in non-small cell lung cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7515922/
https://www.ncbi.nlm.nih.gov/pubmed/32973271
http://dx.doi.org/10.1038/s41598-020-72585-4
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