4.7 Article

Noninvasive Prediction of IDH1 Mutation and ATRX Expression Loss in Low-Grade Gliomas Using Multiparametric MR Radiomic Features

期刊

JOURNAL OF MAGNETIC RESONANCE IMAGING
卷 49, 期 3, 页码 808-817

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WILEY
DOI: 10.1002/jmri.26240

关键词

radiomics; multiparametric MR; IDH1 mutation; loss of ATRX expression; low-grade glioma

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BackgroundNoninvasive detection of isocitrate dehydrogenase 1 mutation (IDH1(+)) and loss of nuclear alpha thalassemia/mental retardation syndrome X-linked expression ((ATRX(-)) are clinically meaningful for molecular stratification of low-grade gliomas (LGGs). PurposeTo study a radiomic approach based on multiparametric MR for noninvasively determining molecular status of IDH1(+) and ATRX(-) in patients with LGG. Study TypeRetrospective, radiomics. PopulationFifty-seven LGG patients with IDH1(+) (n=36 with 19 ATRX(-) and 17 ATRX(+) patients) and IDH1(-) (n=21). Field Strength/Sequence3.0T MRI / 3D arterial spin labeling (3D-ASL), T-2/fluid-attenuated inversion recovery (T(2)FLAIR), and diffusion-weighted imaging (DWI). AssessmentIn all, 265 high-throughput radiomic features were extracted on each tumor volume of interest from T(2)FLAIR and the other three parametric maps of ASL-derived cerebral blood flow (CBF), DWI-derived apparent diffusion coefficient (ADC), and exponential ADC (eADC). Optimal feature subsets were selected as using the support vector machine with a recursive feature elimination algorithm (SVM-RFE). Receiver operating characteristic curve (ROC) analysis was employed to assess the efficiency for identifying the IDH1(+) and ATRX(-) status. Statistical TestsStudent's t-test, chi-square test, and Fisher's exact test were applied to confirm whether intergroup significant differences exist between molecular subtypes decided by IDH1 and ATRX. ResultsOptimal SVM predictive models of IDH1(+) and ATRX(-) were established using 28 features from T(2)Flair, ADC, eADC, and CBF and six features from T(2)Flair, ADC, and CBF. The accuracies/AUCs/sensitivity/specifity/PPV/NPV of predicting IDH1(+) in LGG were 94.74%/0.931/100%/85.71%/92.31%/100%, and those of predicting ATRX(-) in LGG with IDH1(+) were 91.67%/0.926/94.74%/88.24%/90.00%/93.75%, respectively. Data ConclusionUsing the optimal texture features extracted from multiple MR sequences or parametric maps, a promising stratifying strategy was acquired for predicting molecular subtypes of IDH1 and ATRX in LGGs. Level of Evidence: 3 Technical Efficacy Stage: 2 J. Magn. Reson. Imaging 2019;49:808-817.

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