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A retrospective analysis in patients with EGFR-mutant lung adenocarcinoma: is EGFR mutation associated with a higher incidence of brain metastasis?

Lung adenocarcinomas are more commonly associated with brain metastases (BM). Epidermal growth factor receptor (EGFR) mutations have been demonstrated to be both predictive and prognostic for patients with lung adenocarcinoma. We aimed to explore the potential association between EGFR mutation and t...

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Autores principales: Han, Guang, Bi, Jianping, Tan, Wenyong, Wei, Xueyan, Wang, Xiaohong, Ying, Xiaofang, Guo, Xiaofang, Zhou, Xiaoyi, Hu, Desheng, Zhen, Weining
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302968/
https://www.ncbi.nlm.nih.gov/pubmed/27486770
http://dx.doi.org/10.18632/oncotarget.10933
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author Han, Guang
Bi, Jianping
Tan, Wenyong
Wei, Xueyan
Wang, Xiaohong
Ying, Xiaofang
Guo, Xiaofang
Zhou, Xiaoyi
Hu, Desheng
Zhen, Weining
author_facet Han, Guang
Bi, Jianping
Tan, Wenyong
Wei, Xueyan
Wang, Xiaohong
Ying, Xiaofang
Guo, Xiaofang
Zhou, Xiaoyi
Hu, Desheng
Zhen, Weining
author_sort Han, Guang
collection PubMed
description Lung adenocarcinomas are more commonly associated with brain metastases (BM). Epidermal growth factor receptor (EGFR) mutations have been demonstrated to be both predictive and prognostic for patients with lung adenocarcinoma. We aimed to explore the potential association between EGFR mutation and the risk of BM in pulmonary adenocarcinoma patients. Data of 234 patients from 2007 to 2014 were retrospectively reviewed. A total of 108 patients had EGFR mutations in the entire cohort. Among them, 76 patients developed BM during their disease course. The incidence of BM was statistically higher in patients with EGFR mutations both at initial diagnosis (P=0.014) and at last follow-up (P<0.001). Multivariate logistic regression analysis revealed that EGFR mutation significantly increased the risk of BM at initial diagnosis (OR=2.515, P=0.022). In patients without BM at initial diagnosis, the accumulative rate of subsequent BM was significantly higher with EGFR mutations (P=0.001). Multivariate Cox regression analysis identified EGFR mutation as the only independent risk factor for subsequent BM (HR=3.036, P=0.001). Patients with EGFR mutations demonstrated longer overall survival (OS) after BM diagnosis than patients with wild-type EGFR (P=0.028). Our data suggest that EGFR mutation is an independent predictive and prognostic risk factor for BM and a positive predictive factor for OS in patients with BM.
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spelling pubmed-53029682017-02-13 A retrospective analysis in patients with EGFR-mutant lung adenocarcinoma: is EGFR mutation associated with a higher incidence of brain metastasis? Han, Guang Bi, Jianping Tan, Wenyong Wei, Xueyan Wang, Xiaohong Ying, Xiaofang Guo, Xiaofang Zhou, Xiaoyi Hu, Desheng Zhen, Weining Oncotarget Research Paper Lung adenocarcinomas are more commonly associated with brain metastases (BM). Epidermal growth factor receptor (EGFR) mutations have been demonstrated to be both predictive and prognostic for patients with lung adenocarcinoma. We aimed to explore the potential association between EGFR mutation and the risk of BM in pulmonary adenocarcinoma patients. Data of 234 patients from 2007 to 2014 were retrospectively reviewed. A total of 108 patients had EGFR mutations in the entire cohort. Among them, 76 patients developed BM during their disease course. The incidence of BM was statistically higher in patients with EGFR mutations both at initial diagnosis (P=0.014) and at last follow-up (P<0.001). Multivariate logistic regression analysis revealed that EGFR mutation significantly increased the risk of BM at initial diagnosis (OR=2.515, P=0.022). In patients without BM at initial diagnosis, the accumulative rate of subsequent BM was significantly higher with EGFR mutations (P=0.001). Multivariate Cox regression analysis identified EGFR mutation as the only independent risk factor for subsequent BM (HR=3.036, P=0.001). Patients with EGFR mutations demonstrated longer overall survival (OS) after BM diagnosis than patients with wild-type EGFR (P=0.028). Our data suggest that EGFR mutation is an independent predictive and prognostic risk factor for BM and a positive predictive factor for OS in patients with BM. Impact Journals LLC 2016-07-29 /pmc/articles/PMC5302968/ /pubmed/27486770 http://dx.doi.org/10.18632/oncotarget.10933 Text en Copyright: © 2016 Han et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Han, Guang
Bi, Jianping
Tan, Wenyong
Wei, Xueyan
Wang, Xiaohong
Ying, Xiaofang
Guo, Xiaofang
Zhou, Xiaoyi
Hu, Desheng
Zhen, Weining
A retrospective analysis in patients with EGFR-mutant lung adenocarcinoma: is EGFR mutation associated with a higher incidence of brain metastasis?
title A retrospective analysis in patients with EGFR-mutant lung adenocarcinoma: is EGFR mutation associated with a higher incidence of brain metastasis?
title_full A retrospective analysis in patients with EGFR-mutant lung adenocarcinoma: is EGFR mutation associated with a higher incidence of brain metastasis?
title_fullStr A retrospective analysis in patients with EGFR-mutant lung adenocarcinoma: is EGFR mutation associated with a higher incidence of brain metastasis?
title_full_unstemmed A retrospective analysis in patients with EGFR-mutant lung adenocarcinoma: is EGFR mutation associated with a higher incidence of brain metastasis?
title_short A retrospective analysis in patients with EGFR-mutant lung adenocarcinoma: is EGFR mutation associated with a higher incidence of brain metastasis?
title_sort retrospective analysis in patients with egfr-mutant lung adenocarcinoma: is egfr mutation associated with a higher incidence of brain metastasis?
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302968/
https://www.ncbi.nlm.nih.gov/pubmed/27486770
http://dx.doi.org/10.18632/oncotarget.10933
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