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EGFR-TKI-sensitive mutations in lung carcinomas: are they related to clinical features and CT findings?
BACKGROUND: Epidermal growth factor receptor (EGFR) mutation testing is restricted to several limitations. In this study, we examined the relationship between EGFR mutation status and clinicoradiological characteristics in a Chinese cohort of patients. MATERIALS AND METHODS: The data of patients who...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173510/ https://www.ncbi.nlm.nih.gov/pubmed/30323660 http://dx.doi.org/10.2147/CMAR.S174623 |
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author | Qin, Xiaoyi Gu, Xiaolong Lu, Yingru Zhou, Wei |
author_facet | Qin, Xiaoyi Gu, Xiaolong Lu, Yingru Zhou, Wei |
author_sort | Qin, Xiaoyi |
collection | PubMed |
description | BACKGROUND: Epidermal growth factor receptor (EGFR) mutation testing is restricted to several limitations. In this study, we examined the relationship between EGFR mutation status and clinicoradiological characteristics in a Chinese cohort of patients. MATERIALS AND METHODS: The data of patients who were diagnosed with lung carcinoma and underwent both EGFR testing and chest computed tomography (CT) at our hospital between January 1, 2011, and November 31, 2015, were retrospectively analyzed. The age, sex, and smoking index of the patients, the size, margin, and density of the tumor, and the presence of specific signs visible on the CT images were assessed. RESULTS: The results showed a higher rate of EGFR-tyrosine kinase inhibitor (TKI)-sensitive group than nonsensitive group in female patients and patients with a low smoking index (P<0.001, both). In logistic regression analyses, tumor size (P<0.001), smooth margins (P=0.015), and angular margins (P<0.001) were independent negative predictors of EGFR-TKI-sensitive group. Pleural indentation (P<0.001) and air bronchogram (P=0.025) were independent positive predictors of EGFR-TKI-sensitive group. Patients with squamous cell carcinoma had fewer sensitive mutations than those with either adenocarcinoma (P<0.001) or adenosquamous carcinoma (P<0.001). CONCLUSION: Clinical and CT characteristics differed significantly between EGFR-TKI-sensitive and nonsensitive groups. Our findings may be useful in deciding therapeutic strategies for patients in whom EGFR testing is not possible. |
format | Online Article Text |
id | pubmed-6173510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61735102018-10-15 EGFR-TKI-sensitive mutations in lung carcinomas: are they related to clinical features and CT findings? Qin, Xiaoyi Gu, Xiaolong Lu, Yingru Zhou, Wei Cancer Manag Res Original Research BACKGROUND: Epidermal growth factor receptor (EGFR) mutation testing is restricted to several limitations. In this study, we examined the relationship between EGFR mutation status and clinicoradiological characteristics in a Chinese cohort of patients. MATERIALS AND METHODS: The data of patients who were diagnosed with lung carcinoma and underwent both EGFR testing and chest computed tomography (CT) at our hospital between January 1, 2011, and November 31, 2015, were retrospectively analyzed. The age, sex, and smoking index of the patients, the size, margin, and density of the tumor, and the presence of specific signs visible on the CT images were assessed. RESULTS: The results showed a higher rate of EGFR-tyrosine kinase inhibitor (TKI)-sensitive group than nonsensitive group in female patients and patients with a low smoking index (P<0.001, both). In logistic regression analyses, tumor size (P<0.001), smooth margins (P=0.015), and angular margins (P<0.001) were independent negative predictors of EGFR-TKI-sensitive group. Pleural indentation (P<0.001) and air bronchogram (P=0.025) were independent positive predictors of EGFR-TKI-sensitive group. Patients with squamous cell carcinoma had fewer sensitive mutations than those with either adenocarcinoma (P<0.001) or adenosquamous carcinoma (P<0.001). CONCLUSION: Clinical and CT characteristics differed significantly between EGFR-TKI-sensitive and nonsensitive groups. Our findings may be useful in deciding therapeutic strategies for patients in whom EGFR testing is not possible. Dove Medical Press 2018-10-01 /pmc/articles/PMC6173510/ /pubmed/30323660 http://dx.doi.org/10.2147/CMAR.S174623 Text en © 2018 Qin 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 Qin, Xiaoyi Gu, Xiaolong Lu, Yingru Zhou, Wei EGFR-TKI-sensitive mutations in lung carcinomas: are they related to clinical features and CT findings? |
title | EGFR-TKI-sensitive mutations in lung carcinomas: are they related to clinical features and CT findings? |
title_full | EGFR-TKI-sensitive mutations in lung carcinomas: are they related to clinical features and CT findings? |
title_fullStr | EGFR-TKI-sensitive mutations in lung carcinomas: are they related to clinical features and CT findings? |
title_full_unstemmed | EGFR-TKI-sensitive mutations in lung carcinomas: are they related to clinical features and CT findings? |
title_short | EGFR-TKI-sensitive mutations in lung carcinomas: are they related to clinical features and CT findings? |
title_sort | egfr-tki-sensitive mutations in lung carcinomas: are they related to clinical features and ct findings? |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173510/ https://www.ncbi.nlm.nih.gov/pubmed/30323660 http://dx.doi.org/10.2147/CMAR.S174623 |
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