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Early Differentiation of Irreversible Electroporation Ablation Regions with Radiomics Features of Conventional MRI
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9 2022
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Source: Acad Radiol. 29(9):1378-1386
Details:
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Alternative Title:Acad Radiol
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Personal Author:
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Description:Rationale and Objectives:
Irreversible electroporation (IRE) is a promising non-thermal ablation technique for the treatment of patients with hepatocellular carcinoma. Early differentiation of the IRE zone from surrounding reversibly electroporated (RE) penumbra is vital for the evaluation of treatment response. In this study, an advanced statistical learning framework was developed by evaluating standard MRI data to differentiate IRE ablation zones, to correlate with histological tumor biomarkers.
Materials and Methods:
Fourteen rabbits with VX2 liver tumors were scanned following IRE ablation and forty-six features were extracted from T1w and T2w MRI. Following identification of key imaging variables through two-step feature analysis, multivariable classification and regression models were generated for differentiation of IRE ablation zones, and correlation with histological markers reflecting viable tumor cells, microvessel density, and apoptosis rate. The performance of the multivariable models was assessed by measuring accuracy, receiver operating characteristics curve analysis, and Spearman correlation coefficients.
Results:
The classifiers integrating four radiomics features of T1w, T2w, and T1w+T2w MRI data distinguished IRE from RE zones with an accuracy of 97%, 80%, and 97%, respectively. Also, pixelwise classification models of T1w, T2w, and T1w+T2w MRI labeled each voxel with an accuracy of 82.8%, 66.5%, and 82.9%, respectively. Regression models obtained a strong correlation with behavior of viable tumor cells (0.62≤r2≤0.85, p<0.01), apoptosis (0.40≤r2≤0.82, p<0.01), and microvessel density (0.48≤r2≤0.58, p<0.01).
Conclusion:
MRI radiomics features provide descriptive power for early differentiation of IRE and RE zones while observing strong correlations among multivariable MRI regression models and histological tumor biomarkers.
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Pubmed ID:34933803
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Pubmed Central ID:PMC10029937
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Funding:
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Volume:29
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Issue:9
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