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Machine learning based differentiation of glioblastoma from brain metastasis using MRI derived radiomics.

ABSTRACT: Few studies have addressed radiomics based differentiation of Glioblastoma (GBM) and intracranial metastatic disease (IMD). However, the effect of different tumor masks, comparison of single versus multiparametric MRI (mp-MRI) or select combination of sequences remains undefined. We cross-compared multiple radiomics based machine learning (ML) models using mp-MRI to determine optimized configurations. Our retrospective study included 60 GBM and 60 IMD patients. Forty-five combinations of ML models and feature reduction strategies were assessed for features extracted from whole tumor and edema masks using mp-MRI [T1W, T2W, T1-contrast enhanced (T1-CE), ADC, FLAIR], individual MRI sequences and combined T1-CE and FLAIR sequences. Model performance was assessed using receiver operating characteristic curve. For mp-MRI, the best model was LASSO model fit using full feature set (AUC 0.953). FLAIR was the best individual sequence (LASSO-full feature set, AUC 0.951). For combined T1-CE/FLAIR sequence, adaBoost-full feature set was the best performer (AUC 0.951). No significant difference was seen between top models across all scenarios, including models using FLAIR only, mp-MRI and combined T1-CE/FLAIR sequence. Top features were extracted from both the whole tumor and edema masks. Shape sphericity is an important discriminating feature.

SUBMITTER: Priya S

PROVIDER: S-EPMC8131619 | biostudies-literature | 2021 May

REPOSITORIES: biostudies-literature

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Machine learning based differentiation of glioblastoma from brain metastasis using MRI derived radiomics.

Priya Sarv S Liu Yanan Y Ward Caitlin C Le Nam H NH Soni Neetu N Pillenahalli Maheshwarappa Ravishankar R Monga Varun V Zhang Honghai H Sonka Milan M Bathla Girish G

Scientific reports 20210518 1

Few studies have addressed radiomics based differentiation of Glioblastoma (GBM) and intracranial metastatic disease (IMD). However, the effect of different tumor masks, comparison of single versus multiparametric MRI (mp-MRI) or select combination of sequences remains undefined. We cross-compared multiple radiomics based machine learning (ML) models using mp-MRI to determine optimized configurations. Our retrospective study included 60 GBM and 60 IMD patients. Forty-five combinations of ML mode ...[more]

PMID: 34006893

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Project description:BackgroundBrain metastases are common brain tumors in adults. Brain metastases from different primary tumors have special magnetic resonance imaging (MRI) features. As a new technology that can extract and quantify medical image data, and with the rapid development of artificial intelligence, the machine learning model based on radiology has been successfully applied to the diagnosis and differentiation of tumors. This study aimed to develop radiomics models from post-contrast T1-weighted images using machine learning algorithms to differentiate lung cancer from breast cancer brain metastases.MethodsA retrospective analysis was conducted on 118 lung cancer brain metastases patients and 62 breast cancer brain metastases patients confirmed by surgery pathology or combined clinical and imaging diagnosis at The Fifth Affiliated Hospital of Sun Yat-sen University from August 2015 to September 2023. Patients were randomly divided into a training set (126 cases) and a validation set (54 cases) at a 7:3 ratio. Enhanced T1-weighted images of all patients were imported into ITK-SNAP software to manually delineate the region of interest (ROI). Radiomic features were extracted based on the ROI and feature selection was performed using the least absolute shrinkage and selection operator. Significant features were used to develop models using logistic regression (LR), support vector machine (SVM), K-nearest neighbors (KNN), multilayer perceptron (MLP), and light gradient boosting machine (LightGBM). The diagnostic performance of the models was assessed using the receiver operating characteristic (ROC) curve.ResultsThe LightGBM radiomics model exhibited the best diagnostic performance, with an area under the curve (AUC) of 0.875 [95% confidence interval (CI): 0.819-0.931] in the training set and 0.866 (95% CI: 0.740-0.993) in the validation set.ConclusionsThe enhanced MRI radiomics model, especially the LightGBM model, can accurately predict the primary lesion types of brain metastases from lung cancer and breast cancer origins.

Project description:BackgroundDifferentiation between cerebral glioblastoma multiforme (GBM) and solitary brain metastasis (MET) is important. The existing radiomic differentiation method ignores the clinical and routine magnetic resonance imaging (MRI) features.PurposeTo differentiate between GBM and MET and between METs from the lungs (MET-lung) and other sites (MET-other) through clinical and routine MRI, and radiomics analyses.Methods and materialsA total of 350 patients were collected from two institutions, including 182 patients with GBM and 168 patients with MET, which were all proven by pathology. The ROI of the tumor was obtained on axial postcontrast MRI which was performed before operation. Seven radiomic feature selection methods and four classification algorithms constituted 28 classifiers in two classification strategies, with the best classifier serving as the final radiomics model. The clinical and combination models were constructed using the nomograms developed. The performance of the nomograms was evaluated in terms of calibration, discrimination, and clinical usefulness. Student's t-test or the chi-square test was used to assess the differences in the clinical and radiological characteristics between the training and internal validation cohorts. Receiver operating characteristic curve analysis was performed to assess the performance of developed models with the area under the curve (AUC).ResultsThe classifier fisher_decision tree (fisher_DT) showed the best performance (AUC: 0.696, 95% CI:0.608-0.783) for distinguishing between GBM and MET in internal validation cohorts; the classifier reliefF_random forest (reliefF_RF) showed the best performance (AUC: 0.759, 95% CI: 0.613-0.904) for distinguishing between MET-lung and MET-other in internal validation cohorts. The combination models incorporating the radiomics signature and clinical-radiological characteristics were superior to the clinical-radiological models in the two classification strategies (AUC: 0.764 for differentiation between GBM in internal validation cohorts and MET and 0.759 or differentiation between MET-lung and MET-other in internal validation cohorts). The nomograms showed satisfactory performance and calibration and were considered clinically useful, as revealed in the decision curve analysis.Data conclusionThe combination of radiomic and non-radiomic features is helpful for the differentiation among GBM, MET-lung, and MET-other.

Project description:Background:To evaluate the association of multiparametric and multiregional MRI-features with key molecular characteristics in patients with newly-diagnosed glioblastoma. Methods:Retrospective data evaluation was approved by the local ethics committee of the University of Heidelberg (ethics approval number: S-320/2012) and informed consent was waived. Preoperative MRI-features were correlated with key molecular characteristics within a single-institutional cohort of 152 patients with newly-diagnosed glioblastoma. Preoperative MRI-features (n=31) included multiparametric (anatomical, diffusion-, perfusion-, and susceptibility-weighted images) and multiregional (contrast enhancing and non-enhancing FLAIR-hyperintense) information with (histogram) quantification of tumor volumes, volume ratios, apparent diffusion coefficients, cerebral blood flow / volume (CBF / CBV) and intratumoral susceptibility signals. Molecular characteristics determined with the Illumina Infinium HumanMethylation450 array included global DNA-methylation subgroups (e.g. mesenchymal (MES), RTK I “PGFRA”, RTK II “classic”), MGMT-promoter methylation status and hallmark copy-number-variations (EGFR-, PDGFRA-, MDM4- and CDK4-amplification; PTEN-, CDKN2A-, NF1- and RB1-loss). Univariate analyses (voxel-lesion-symptom-mapping for tumor location, Wilcoxon-test for all other MRI-features) as well as machine-learning models were applied to study the strength of association and discriminative value of MRI-features for predicting underlying molecular characteristics. Results: There was no tumor location predilection for any of the assessed molecular parameters (permutation-adjusted p>0.05 each). Univariate imaging parameter associations were noted for EGFR amplification and CDKN2A loss, both demonstrating increased nrCBV and nrCBF values (performance of these parameters, as assessed by the area under the ROC curve ranged from 63 to 69%, FDR-adjusted p<0.05, respectively). Subjecting all MRI-features to machine-learning-based classification allowed to predict EGFR amplification status and the RTK II “classic” GB subgroup with a moderate, yet significantly greater accuracy (63% for EGFR [p<0.01] and 61% for RTK II [p=0.01]) than the prediction by chance, whereas prediction accuracy for all other molecular parameters was non-significant (p>0.05, all models). Conclusions: In summary, we found univariate associations between established MRI-features and molecular characteristics, however not of sufficient strength to allow the generation of machine-learning classification models for reliable and clinically meaningful prediction of the assessed molecular characteristics in patients with newly-diagnosed glioblastoma.

Dataset Information

Machine learning based differentiation of glioblastoma from brain metastasis using MRI derived radiomics.

Publications

Machine learning based differentiation of glioblastoma from brain metastasis using MRI derived radiomics.

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