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The relationship of plasma fibrinogen with clinicopathological stages and tumor markers in patients with non-small cell lung cancer

Numerous studies have shown that the blood of cancer patients are generally in hypercoagulable statement. The aim of the present research is to study the relationships of plasma fibrinogen (Fbg) levels with clinicopathological stages (CS) and tumor markers of non-small cell lung cancer (NSCLC). Base...

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Autores principales: Bian, Nan-Nan, Shi, Xin-Yu, Qi, Hong-Yu, Hu, Xin, Ge, Yang, An, Guang-Yu, Feng, Guo-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708950/
https://www.ncbi.nlm.nih.gov/pubmed/31393394
http://dx.doi.org/10.1097/MD.0000000000016764
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author Bian, Nan-Nan
Shi, Xin-Yu
Qi, Hong-Yu
Hu, Xin
Ge, Yang
An, Guang-Yu
Feng, Guo-Sheng
author_facet Bian, Nan-Nan
Shi, Xin-Yu
Qi, Hong-Yu
Hu, Xin
Ge, Yang
An, Guang-Yu
Feng, Guo-Sheng
author_sort Bian, Nan-Nan
collection PubMed
description Numerous studies have shown that the blood of cancer patients are generally in hypercoagulable statement. The aim of the present research is to study the relationships of plasma fibrinogen (Fbg) levels with clinicopathological stages (CS) and tumor markers of non-small cell lung cancer (NSCLC). Baseline information, plasma Fbg levels, CS, and expression level of tumor markers were collected from medical records retrospectively. Unitary linear regression was used to analyze the relationships between continuous variables and Fbg, and multiple linear regression was used to analyze the relationships between categorical variables and Fbg. National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology (Version 4) for NSCLC were adopted to evaluate CS. A total of 652 NSCLC patients were included. Compared with the females, male patients had higher mean plasma Fbg levels (P < .001). The later the N stages (P = .002), M stages (P = .002), and CS (P = .001) were, the higher the average plasma Fbg levels were. The levels of squamous cell carcinoma antigen (P = .001), carbohydrate antigen 125 (P = .041), and neuron-specific enolase (P < .001) were positively correlated with plasma Fbg concentration. The plasma level of Fbg in lung adenocarcinoma patients (P < .001) was the lowest, while that of lung squamous cell carcinoma patients (P < .001) was the highest in NSCLC patients. The plasma Fbg concentration is related to gender, CS, and tumor markers in patients with NSCLC.
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spelling pubmed-67089502019-10-01 The relationship of plasma fibrinogen with clinicopathological stages and tumor markers in patients with non-small cell lung cancer Bian, Nan-Nan Shi, Xin-Yu Qi, Hong-Yu Hu, Xin Ge, Yang An, Guang-Yu Feng, Guo-Sheng Medicine (Baltimore) Research Article Numerous studies have shown that the blood of cancer patients are generally in hypercoagulable statement. The aim of the present research is to study the relationships of plasma fibrinogen (Fbg) levels with clinicopathological stages (CS) and tumor markers of non-small cell lung cancer (NSCLC). Baseline information, plasma Fbg levels, CS, and expression level of tumor markers were collected from medical records retrospectively. Unitary linear regression was used to analyze the relationships between continuous variables and Fbg, and multiple linear regression was used to analyze the relationships between categorical variables and Fbg. National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology (Version 4) for NSCLC were adopted to evaluate CS. A total of 652 NSCLC patients were included. Compared with the females, male patients had higher mean plasma Fbg levels (P < .001). The later the N stages (P = .002), M stages (P = .002), and CS (P = .001) were, the higher the average plasma Fbg levels were. The levels of squamous cell carcinoma antigen (P = .001), carbohydrate antigen 125 (P = .041), and neuron-specific enolase (P < .001) were positively correlated with plasma Fbg concentration. The plasma level of Fbg in lung adenocarcinoma patients (P < .001) was the lowest, while that of lung squamous cell carcinoma patients (P < .001) was the highest in NSCLC patients. The plasma Fbg concentration is related to gender, CS, and tumor markers in patients with NSCLC. Wolters Kluwer Health 2019-08-09 /pmc/articles/PMC6708950/ /pubmed/31393394 http://dx.doi.org/10.1097/MD.0000000000016764 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Bian, Nan-Nan
Shi, Xin-Yu
Qi, Hong-Yu
Hu, Xin
Ge, Yang
An, Guang-Yu
Feng, Guo-Sheng
The relationship of plasma fibrinogen with clinicopathological stages and tumor markers in patients with non-small cell lung cancer
title The relationship of plasma fibrinogen with clinicopathological stages and tumor markers in patients with non-small cell lung cancer
title_full The relationship of plasma fibrinogen with clinicopathological stages and tumor markers in patients with non-small cell lung cancer
title_fullStr The relationship of plasma fibrinogen with clinicopathological stages and tumor markers in patients with non-small cell lung cancer
title_full_unstemmed The relationship of plasma fibrinogen with clinicopathological stages and tumor markers in patients with non-small cell lung cancer
title_short The relationship of plasma fibrinogen with clinicopathological stages and tumor markers in patients with non-small cell lung cancer
title_sort relationship of plasma fibrinogen with clinicopathological stages and tumor markers in patients with non-small cell lung cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708950/
https://www.ncbi.nlm.nih.gov/pubmed/31393394
http://dx.doi.org/10.1097/MD.0000000000016764
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