A Fully Automated Deep-Learning Model for Predicting the Molecular Subtypes of Posterior Fossa Ependymomas Using T2-Weighted Images

Author:

Cheng Dan1ORCID,Zhuo Zhizheng1ORCID,Du Jiang2ORCID,Weng Jinyuan3ORCID,Zhang Chengzhou4ORCID,Duan Yunyun1ORCID,Sun Ting1ORCID,Wu Minghao1ORCID,Guo Min1ORCID,Hua Tiantian1ORCID,Jin Ying1ORCID,Peng Boyang1ORCID,Li Zhaohui5ORCID,Zhu Mingwang6ORCID,Imami Maliha7ORCID,Bettegowda Chetan8ORCID,Sair Haris7ORCID,Bai Harrison X.7ORCID,Barkhof Frederik910ORCID,Liu Xing2ORCID,Liu Yaou1ORCID

Affiliation:

1. 1Department of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, P.R. China.

2. 2Department of Neuropathology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.

3. 3Department of Medical Imaging Product, Neusoft, Group Ltd., Shenyang, P.R. China.

4. 4Department of Radiology, Yantai Yuhuangding Hospital, Yantai, Shandong, P.R. China.

5. 5BioMind Inc., Beijing, P.R. China.

6. 6Department of Radiology, Sanbo Brain Hospital, Capital Medical University, Beijing, P.R. China.

7. 7Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland.

8. 8Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.

9. 9Queen Square Institute of Neurology and Centre for Medical Image Computing, University College London, London, United Kingdom.

10. 10Department of Radiology & Nuclear Medicine, Amsterdam UMC, Vrije Universiteit, the Netherlands.

Abstract

Abstract Purpose: We aimed to develop and validate a deep learning (DL) model to automatically segment posterior fossa ependymoma (PF-EPN) and predict its molecular subtypes [Group A (PFA) and Group B (PFB)] from preoperative MR images. Experimental Design: We retrospectively identified 227 PF-EPNs (development and internal test sets) with available preoperative T2-weighted (T2w) MR images and molecular status to develop and test a 3D nnU-Net (referred to as T2-nnU-Net) for tumor segmentation and molecular subtype prediction. The network was externally tested using an external independent set [n = 40; subset-1 (n = 31) and subset-2 (n =9)] and prospectively enrolled cases [prospective validation set (n = 27)]. The Dice similarity coefficient was used to evaluate the segmentation performance. Receiver operating characteristic analysis for molecular subtype prediction was performed. Results: For tumor segmentation, the T2-nnU-Net achieved a Dice score of 0.94 ± 0.02 in the internal test set. For molecular subtype prediction, the T2-nnU-Net achieved an AUC of 0.93 and accuracy of 0.89 in the internal test set, an AUC of 0.99 and accuracy of 0.93 in the external test set. In the prospective validation set, the model achieved an AUC of 0.93 and an accuracy of 0.89. The predictive performance of T2-nnU-Net was superior or comparable to that of demographic and multiple radiologic features (AUCs ranging from 0.87 to 0.95). Conclusions: A fully automated DL model was developed and validated to accurately segment PF-EPNs and predict molecular subtypes using only T2w MR images, which could help in clinical decision-making.

Funder

National Science Foundation of China

Beijing Municipal Natural Science Foundation for Distinguished Young Scholars

Beijing Youth Scholar, and the Special Fund of the Pediatric Medical Coordinated Development Center of Beijing Hospital Authority

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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