Machine-learning based classification of glioblastoma using delta-radiomic features derived from dynamic susceptibility contrast enhanced magnetic resonance images

• Type of Material: Article
• Authors: Jiwoong Jeong, Emory University; Liya Wang, Emory University; Bing Ji, Emory University; Yang Lei, Emory University; Arif Ali, Emory University; Tian Liu, Emory University; Walter J Curran, Emory University; Hui Mao, Emory University; Xiaofeng Yang, Emory University
• Language: English
• Date: 2019-07-01
• Publisher: AME Publishing Company
• Publication Version: Final Published Version
• Copyright Statement: © 2019 AME Publishing Company. All rights reserved.
• Final Published Version (URL): http://dx.doi.org/10.21037/qims.2019.07.01
• Title of Journal or Parent Work: Quantitative imaging in medicine and surgery
• ISSN: 2223-4292
• Volume: 9
• Issue: 7
• Start Page: 1201
• End Page: 1213
• Grant/Funding Information: This work was supported in parts by grants from National Institutes of Health (R01CA215718 to X Yang, R01CA203388 and R01CA169937 to H Mao); and Emory Winship Cancer Institute pilot grant.
• Keywords: GLIOMA; dynamic susceptibility contrast enhanced magnetic resonance imaging (DSC MRI); MRI; Science & Technology; radiomics; Machine learning; RADIOTHERAPY; Life Sciences & Biomedicine; IDH1; HETEROGENEITY; Radiology, Nuclear Medicine & Medical Imaging; TEXTURE ANALYSIS
• Research Categories: Health Sciences, Oncology; Health Sciences, Medicine and Surgery; Health Sciences, Radiology

Abstract

Background: Glioblastoma is the most aggressive brain tumor with poor prognosis. The purpose of this study is to improve the tissue characterization of these highly heterogeneous tumors using delta-radiomic features of images from dynamic susceptibility contrast enhanced (DSC) magnetic resonance imaging (MRI). Methods: Twenty-five patients with histopathologically confirmed to be 13 high-grade (HG) and 12 lowgrade (LG) gliomas who underwent the standard brain tumor MRI protocol, including DSC MRI, were included. Tumor regions on all DSC MRI images were registered to and contoured in T2-weighted fluidattenuated inversion recovery (FLAIR) images. These contours and its contralateral regions of the normal tissue were used to extract delta-radiomic features before applying feature selection. The most informative and non-redundant features were selected to train a random forest to differentiate HG and LG gliomas. Then a leave-one-out cross-validation random forest was applied to classify these tumors for grading. Finally, a majority-voting method was applied to reduce binarization bias and to combine the results of various feature lists. Results: Analysis of the predictions showed that the reported method consistently predicted the tumor grade of 24 out of 25 patients correctly (0.96). Finally, the mean prediction accuracy was 0.950±0.091 for HG and 0.850±0.255 for LG. The area under the receiver operating characteristic curve (AUC) was 0.94. Conclusions: This study shows that delta-radiomic features derived from DSC MRI data can be used to characterize and determine the tumor grades. The radiomic features from DSC MRI may be used to elucidate the underlying tumor biology and response to therapy.