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. 2020 Jul 21;10(1):12110.
doi: 10.1038/s41598-020-68980-6.

Robust performance of deep learning for distinguishing glioblastoma from single brain metastasis using radiomic features: model development and validation

Affiliations

Robust performance of deep learning for distinguishing glioblastoma from single brain metastasis using radiomic features: model development and validation

Sohi Bae et al. Sci Rep. .

Abstract

We evaluated the diagnostic performance and generalizability of traditional machine learning and deep learning models for distinguishing glioblastoma from single brain metastasis using radiomics. The training and external validation cohorts comprised 166 (109 glioblastomas and 57 metastases) and 82 (50 glioblastomas and 32 metastases) patients, respectively. Two-hundred-and-sixty-five radiomic features were extracted from semiautomatically segmented regions on contrast-enhancing and peritumoral T2 hyperintense masks and used as input data. For each of a deep neural network (DNN) and seven traditional machine learning classifiers combined with one of five feature selection methods, hyperparameters were optimized through tenfold cross-validation in the training cohort. The diagnostic performance of the optimized models and two neuroradiologists was tested in the validation cohort for distinguishing glioblastoma from metastasis. In the external validation, DNN showed the highest diagnostic performance, with an area under receiver operating characteristic curve (AUC), sensitivity, specificity, and accuracy of 0.956 (95% confidence interval [CI], 0.918-0.990), 90.6% (95% CI, 80.5-100), 88.0% (95% CI, 79.0-97.0), and 89.0% (95% CI, 82.3-95.8), respectively, compared to the best-performing traditional machine learning model (adaptive boosting combined with tree-based feature selection; AUC, 0.890 (95% CI, 0.823-0.947)) and human readers (AUC, 0.774 [95% CI, 0.685-0.852] and 0.904 [95% CI, 0.852-0.951]). The results demonstrated deep learning using radiomic features can be useful for distinguishing glioblastoma from metastasis with good generalizability.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Flow chart of patient inclusion. T2WI T2-weighted image, 3D CE-T1WI three-dimensional contrast-enhanced T1-weighted image, IDH isocitrate dehydrogenase.
Figure 2
Figure 2
Heatmap depicting the mean area under the receiver operating characteristic curve of five machine learning classifier (columns) and seven feature selection (rows) methods in the training set. (A) CE mask alone, (B) PT mask alone, (C) CE and PT masks combined. CE contrast-enhancing, PT peritumoral T2 hyperintense, MI mutual information, RFE  recursive feature elimination, Lasso least absolute shrinkage and selection operator, kNN k-nearest neighbor, NB naïve Bayes, RF random forest, Ada adaptive boosting, L-SVM linear support vector machine, R-SVM radial basis function support vector machine, LDA linear discriminant analysis.
Figure 3
Figure 3
Pipeline of the study. CE contrast-enhancing, PT peritumoral T2 hyperintense, CE-T1WI contrast-enhanced T1-weighted image, T2WI T2-weighted image, GLCM gray level co-occurrence matrix, GLRLM gray level run length matrix, GLSZM gray level size zone matrix, NGTDM neighboring gray tone difference matrix, MI mutual information, RFE recursive feature elimination, Lasso least absolute shrinkage and selection operator, kNN k-nearest neighbor, NB naïve Bayes, RF random forest, Ada adaptive boosting, L-SVM linear support vector machine, R-SVM radial basis function support vector machine, LDA linear discriminant analysis, AUC area under the receiver operating characteristic curve.

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