Quantitative Biomarkers for Prediction of Epidermal Growth Factor Receptor Mutation in Non-Small Cell Lung Cancer
OBJECTIVES: To predict epidermal growth factor receptor (EGFR) mutation status using quantitative radiomic biomarkers and representative clinical variables. METHODS: The study included 180 patients diagnosed as of non-small cell lung cancer (NSCLC) with their pre-therapy computed tomography (CT) sca...
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doaj-660ae76adcb948e59cf87df5a481ad532020-11-24T21:05:58ZengElsevierTranslational Oncology1936-52331944-71242018-02-011119410110.1016/j.tranon.2017.10.012Quantitative Biomarkers for Prediction of Epidermal Growth Factor Receptor Mutation in Non-Small Cell Lung CancerLiwen Zhang0Bojiang Chen1Xia Liu2Jiangdian Song3Mengjie Fang4Chaoen Hu5Di Dong6Weimin Li7Jie Tian8School of automation, Harbin University of Science and Technology, Harbin, Heilongjiang, 150080, ChinaDepartment of respiratory and critical care medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, ChinaSchool of automation, Harbin University of Science and Technology, Harbin, Heilongjiang, 150080, ChinaSchool of Medical Informatics, China Medical University, Shenyang, Liaoning 110122, ChinaCAS Key Lab of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, 100190, ChinaCAS Key Lab of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, 100190, ChinaCAS Key Lab of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, 100190, ChinaDepartment of respiratory and critical care medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, ChinaCAS Key Lab of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, 100190, ChinaOBJECTIVES: To predict epidermal growth factor receptor (EGFR) mutation status using quantitative radiomic biomarkers and representative clinical variables. METHODS: The study included 180 patients diagnosed as of non-small cell lung cancer (NSCLC) with their pre-therapy computed tomography (CT) scans. Using a radiomic method, 485 features that reflect the heterogeneity and phenotype of tumors were extracted. Afterwards, these radiomic features were used for predicting epidermal growth factor receptor (EGFR) mutation status by a least absolute shrinkage and selection operator (LASSO) based on multivariable logistic regression. As a result, we found that radiomic features have prognostic ability in EGFR mutation status prediction. In addition, we used radiomic nomogram and calibration curve to test the performance of the model. RESULTS: Multivariate analysis revealed that the radiomic features had the potential to build a prediction model for EGFR mutation. The area under the receiver operating characteristic curve (AUC) for the training cohort was 0.8618, and the AUC for the validation cohort was 0.8725, which were superior to prediction model that used clinical variables alone. CONCLUSION: Radiomic features are better predictors of EGFR mutation status than conventional semantic CT image features or clinical variables to help doctors to decide who need EGFR tyrosine kinase inhibitor (TKI) treatment.http://www.sciencedirect.com/science/article/pii/S1936523317302619 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Liwen Zhang Bojiang Chen Xia Liu Jiangdian Song Mengjie Fang Chaoen Hu Di Dong Weimin Li Jie Tian |
spellingShingle |
Liwen Zhang Bojiang Chen Xia Liu Jiangdian Song Mengjie Fang Chaoen Hu Di Dong Weimin Li Jie Tian Quantitative Biomarkers for Prediction of Epidermal Growth Factor Receptor Mutation in Non-Small Cell Lung Cancer Translational Oncology |
author_facet |
Liwen Zhang Bojiang Chen Xia Liu Jiangdian Song Mengjie Fang Chaoen Hu Di Dong Weimin Li Jie Tian |
author_sort |
Liwen Zhang |
title |
Quantitative Biomarkers for Prediction of Epidermal Growth Factor Receptor Mutation in Non-Small Cell Lung Cancer |
title_short |
Quantitative Biomarkers for Prediction of Epidermal Growth Factor Receptor Mutation in Non-Small Cell Lung Cancer |
title_full |
Quantitative Biomarkers for Prediction of Epidermal Growth Factor Receptor Mutation in Non-Small Cell Lung Cancer |
title_fullStr |
Quantitative Biomarkers for Prediction of Epidermal Growth Factor Receptor Mutation in Non-Small Cell Lung Cancer |
title_full_unstemmed |
Quantitative Biomarkers for Prediction of Epidermal Growth Factor Receptor Mutation in Non-Small Cell Lung Cancer |
title_sort |
quantitative biomarkers for prediction of epidermal growth factor receptor mutation in non-small cell lung cancer |
publisher |
Elsevier |
series |
Translational Oncology |
issn |
1936-5233 1944-7124 |
publishDate |
2018-02-01 |
description |
OBJECTIVES: To predict epidermal growth factor receptor (EGFR) mutation status using quantitative radiomic biomarkers and representative clinical variables. METHODS: The study included 180 patients diagnosed as of non-small cell lung cancer (NSCLC) with their pre-therapy computed tomography (CT) scans. Using a radiomic method, 485 features that reflect the heterogeneity and phenotype of tumors were extracted. Afterwards, these radiomic features were used for predicting epidermal growth factor receptor (EGFR) mutation status by a least absolute shrinkage and selection operator (LASSO) based on multivariable logistic regression. As a result, we found that radiomic features have prognostic ability in EGFR mutation status prediction. In addition, we used radiomic nomogram and calibration curve to test the performance of the model. RESULTS: Multivariate analysis revealed that the radiomic features had the potential to build a prediction model for EGFR mutation. The area under the receiver operating characteristic curve (AUC) for the training cohort was 0.8618, and the AUC for the validation cohort was 0.8725, which were superior to prediction model that used clinical variables alone. CONCLUSION: Radiomic features are better predictors of EGFR mutation status than conventional semantic CT image features or clinical variables to help doctors to decide who need EGFR tyrosine kinase inhibitor (TKI) treatment. |
url |
http://www.sciencedirect.com/science/article/pii/S1936523317302619 |
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