Abstract

The peritumoral region (PTR) of glioblastoma (GBM) appears as a T2W-hyperintensity and is composed of microscopic tumor and edema. Infiltrative low grade glioma (LGG) comprises tumor cells that seem similar to GBM PTR on MRI. The work here explored if a radiomics-based approach can distinguish between the two groups (tumor and edema versus tumor alone). Patients with GBM and LGG imaged using a 1.5T MRI were included in the study. Image data from cases of GBM PTR, and LGG were manually segmented guided by T2W hyperintensity. A set of 91 first-order and texture features were determined from each of T1W-contrast, and T2W-FLAIR, diffusion-weighted imaging sequences. Applying filtration techniques, a total of 3822 features were obtained. Different feature reduction techniques were employed, and a subsequent model was constructed using four machine learning classifiers. Leave-one-out cross-validation was used to assess classifier performance. The analysis included 42 GBM and 36 LGG. The best performance was obtained using AdaBoost classifier using all the features with a sensitivity, specificity, accuracy, and area of curve (AUC) of 91%, 86%, 89%, and 0.96, respectively. Amongst the feature selection techniques, the recursive feature elimination technique had the best results, with an AUC ranging from 0.87 to 0.92. Evaluation with the F-test resulted in the most consistent feature selection with 3 T1W-contrast texture features chosen in over 90% of instances. Quantitative analysis of conventional MRI sequences can effectively demarcate GBM PTR from LGG, which is otherwise indistinguishable on visual estimation.

Highlights

  • Radiomics is an emerging field in medicine and oncology involving quantitative feature analysis of highquality radiographic images [1, 2]

  • Infiltrative low grade glioma (LGG) comprises tumor cells that seem similar to GBM peritumoral region (PTR) on Magnetic resonance imaging (MRI)

  • The work here explored if a radiomics-based approach can distinguish between LGG and GBM PTR, which can have future implications on existing treatment paradigms

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Summary

Introduction

Radiomics is an emerging field in medicine and oncology involving quantitative feature analysis of highquality radiographic images [1, 2]. Radiomic analysis has been widely undertaken in various CNS tumors, including gliomas, aiding in the differentiation between tumor histologies, grading, genetic profiling, and prognostication [5, 6]. We refer to grade 2 infiltrative gliomas as low-grade glioma (LGG), which typically are identified on MRI as T2-W hyperintense lesions. On MRI, distinct anatomical compartments can be identified in GBM, including tumor enhancement appearing as contrast-enhancing regions on T1-W sequences, with a central non-enhancing necrotic core and the adjacent peritumoural region (PTR) appearing as a T2-Weighted hyperintense area. In LGG, the areas of T2-W hyperintensity represent tumor, whereas GBM PTR is an admixture of microscopic infiltrative tumor and vasogenic edema [8, 9]. Infiltrative low grade glioma (LGG) comprises tumor cells that seem similar to GBM PTR on MRI. The work here explored if a radiomics-based approach can distinguish between LGG and GBM PTR, which can have future implications on existing treatment paradigms

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