Fully automated hybrid approach to predict the IDH mutation status of gliomas via deep learning and radiomics

Author:

Choi Yoon Seong123ORCID,Bae Sohi4,Chang Jong Hee5,Kang Seok-Gu5,Kim Se Hoon6,Kim Jinna3,Rim Tyler Hyungtaek7,Choi Seung Hong8,Jain Rajan910,Lee Seung-Koo3

Affiliation:

1. Duke-NUS Medical School, RADSC ACP, Singapore

2. Department of Diagnostic Radiology, Singapore General Hospital, Singapore

3. Department of Radiology and Research Institute of Radiological Science, Yonsei University College of Medicine, Seoul, Korea

4. Department of Radiology, National Health Insurance Service Ilsan Hospital, Goyang, Korea

5. Department of Neurosurgery, Yonsei University College of Medicine, Seoul, Korea

6. Department of Pathology, Yonsei University College of Medicine, Seoul, Korea

7. Singapore Eye Research Institute, Singapore National Eye Centre, Duke-NUS Medical School, Singapore

8. Department of Radiology, Seoul National University College of Medicine, Seoul, Korea

9. Department of Radiology, New York University School of Medicine, New York, New York, USA

10. Department of Neurosurgery, New York University School of Medicine, New York, New York, USA

Abstract

Abstract Background Glioma prognosis depends on isocitrate dehydrogenase (IDH) mutation status. We aimed to predict the IDH status of gliomas from preoperative MR images using a fully automated hybrid approach with convolutional neural networks (CNNs) and radiomics. Methods We reviewed 1166 preoperative MR images of gliomas (grades II–IV) from Severance Hospital (n = 856), Seoul National University Hospital (SNUH; n = 107), and The Cancer Imaging Archive (TCIA; n = 203). The Severance set was subdivided into the development (n = 727) and internal test (n = 129) sets. Based on T1 postcontrast, T2, and fluid-attenuated inversion recovery images, a fully automated model was developed that comprised a CNN for tumor segmentation (Model 1) and CNN-based classifier for IDH status prediction (Model 2) that uses a hybrid approach based on 2D tumor images and radiomic features from 3D tumor shape and loci guided by Model 1. The trained model was tested on internal (a subset of the Severance set) and external (SNUH and TCIA) test sets. Results The CNN for tumor segmentation (Model 1) achieved a dice coefficient of 0.86–0.92 across datasets. Our hybrid model achieved accuracies of 93.8%, 87.9%, and 78.8%, with areas under the receiver operating characteristic curves of 0.96, 0.94, and 0.86 and areas under the precision-recall curves of 0.88, 0.82, and 0.81 in the internal test, SNUH, and TCIA sets, respectively. Conclusions Our fully automated hybrid model demonstrated the potential to be a highly reproducible and generalizable tool across different datasets for the noninvasive prediction of the IDH status of gliomas.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Clinical Neurology,Oncology

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