Deep learning-based automatic tumor burden assessment of pediatric high-grade gliomas, medulloblastomas, and other leptomeningeal seeding tumors

Author:

Peng Jian1,Kim Daniel D2,Patel Jay B3,Zeng Xiaowei1,Huang Jiaer4,Chang Ken3,Xun Xinping1,Zhang Chen1,Sollee John2,Wu Jing5,Dalal Deepa J6,Feng Xue7,Zhou Hao8,Zhu Chengzhang14,Zou Beiji4,Jin Ke9,Wen Patrick Y10,Boxerman Jerrold L2,Warren Katherine E11,Poussaint Tina Y12,States Lisa J6,Kalpathy-Cramer Jayashree3,Yang Li1,Huang Raymond Y13,Bai Harrison X2ORCID

Affiliation:

1. Department of Neurology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China

2. Department of Diagnostic Imaging, Rhode Island Hospital and Alpert Medical School of Brown University, Providence, Rhode Island, USA

3. Department of Radiology, Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA

4. School of Computer Science and Engineering, Central South University, Changsha, Hunan, China

5. Department of Radiology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China

6. Department of Radiology, Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, USA

7. Department of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, USA

8. Department of Neurology, Xiangya Hospital of Central South University, Changsha, Hunan, China

9. Department of Radiology, Hunan Children’s Hospital, Changsha, Hunan, China

10. Center for Neuro-Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA

11. Department of Pediatrics, Dana Farber Cancer Institute, Boston, Massachusetts, USA

12. Department of Radiology, Boston Children’s Hospital, Boston, Massachusetts, USA

13. Department of Radiology, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA

Abstract

Abstract Background Longitudinal measurement of tumor burden with magnetic resonance imaging (MRI) is an essential component of response assessment in pediatric brain tumors. We developed a fully automated pipeline for the segmentation of tumors in pediatric high-grade gliomas, medulloblastomas, and leptomeningeal seeding tumors. We further developed an algorithm for automatic 2D and volumetric size measurement of tumors. Methods The preoperative and postoperative cohorts were randomly split into training and testing sets in a 4:1 ratio. A 3D U-Net neural network was trained to automatically segment the tumor on T1 contrast-enhanced and T2/FLAIR images. The product of the maximum bidimensional diameters according to the RAPNO (Response Assessment in Pediatric Neuro-Oncology) criteria (AutoRAPNO) was determined. Performance was compared to that of 2 expert human raters who performed assessments independently. Volumetric measurements of predicted and expert segmentations were computationally derived and compared. Results A total of 794 preoperative MRIs from 794 patients and 1003 postoperative MRIs from 122 patients were included. There was excellent agreement of volumes between preoperative and postoperative predicted and manual segmentations, with intraclass correlation coefficients (ICCs) of 0.912 and 0.960 for the 2 preoperative and 0.947 and 0.896 for the 2 postoperative models. There was high agreement between AutoRAPNO scores on predicted segmentations and manually calculated scores based on manual segmentations (Rater 2 ICC = 0.909; Rater 3 ICC = 0.851). Lastly, the performance of AutoRAPNO was superior in repeatability to that of human raters for MRIs with multiple lesions. Conclusions Our automated deep learning pipeline demonstrates potential utility for response assessment in pediatric brain tumors. The tool should be further validated in prospective studies.

Funder

Natural Science Foundation of China

Sheng Hua Yu-Ying Project of Central South University

National Institute of Biomedical Imaging and Bioengineering

National Institutes of Health

High-tech Industry of Hunan Province

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

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