Noninvasive Molecular Subtyping of Pediatric Low-Grade Glioma with Self-Supervised Transfer Learning.

Radiol Artif Intell

From the Artificial Intelligence in Medicine Program, Mass General Brigham, Harvard Medical School, Boston, Mass (D.T., Z.Y., A.Z., Y.Z., A.B., R.C., H.H., H.J.W.L.A., B.H.K.); Department of Radiation Oncology, Dana-Farber Cancer Institute, Brigham and Women's Hospital, Boston Children's Hospital, Harvard Medical School, 75 Francis St, Boston, MA 02115 (D.T., Z.Y., A.Z., Y.Z., A.B., R.C., H.H., K.X.L., H.E., H.J.W.L.A., D.A.H.K., B.H.K.); Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, Mass (S.V., S.P.P., T.Y.P.); Center for Data-Driven Discovery in Biomedicine (A.N., A.F.) and Department of Neurosurgery (A.F., A.C.R.), Children's Hospital of Philadelphia, Philadelphia, Pa; Department of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pa (A.N.); Departments of Neurology, Pediatrics, and Neurologic Surgery, University of California San Francisco, San Francisco, Calif (S.M.); Department of Radiology, Brigham and Women's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Mass (H.J.W.L.A.); Department of Radiology and Nuclear Medicine, CalifRIM & GROW, Maastricht University, Maastricht, the Netherlands (H.J.W.L.A.); and Department of Pediatric Oncology (P.B.) and Department of Pathology (K.L.L.), Dana-Farber Cancer Institute, Boston Children's Hospital, Harvard Medical School, Boston, Mass.

Published: May 2024

Purpose To develop and externally test a scan-to-prediction deep learning pipeline for noninvasive, MRI-based mutational status classification for pediatric low-grade glioma. Materials and Methods This retrospective study included two pediatric low-grade glioma datasets with linked genomic and diagnostic T2-weighted MRI data of patients: Dana-Farber/Boston Children's Hospital (development dataset, = 214 [113 (52.8%) male; 104 (48.6%) wild type, 60 (28.0%) fusion, and 50 (23.4%) V600E]) and the Children's Brain Tumor Network (external testing, = 112 [55 (49.1%) male; 35 (31.2%) wild type, 60 (53.6%) fusion, and 17 (15.2%) V600E]). A deep learning pipeline was developed to classify mutational status ( wild type vs fusion vs V600E) via a two-stage process: three-dimensional tumor segmentation and extraction of axial tumor images and section-wise, deep learning-based classification of mutational status. Knowledge-transfer and self-supervised approaches were investigated to prevent model overfitting, with a primary end point of the area under the receiver operating characteristic curve (AUC). To enhance model interpretability, a novel metric, center of mass distance, was developed to quantify the model attention around the tumor. Results A combination of transfer learning from a pretrained medical imaging-specific network and self-supervised label cross-training (TransferX) coupled with consensus logic yielded the highest classification performance with an AUC of 0.82 (95% CI: 0.72, 0.91), 0.87 (95% CI: 0.61, 0.97), and 0.85 (95% CI: 0.66, 0.95) for wild type, fusion, and V600E, respectively, on internal testing. On external testing, the pipeline yielded an AUC of 0.72 (95% CI: 0.64, 0.86), 0.78 (95% CI: 0.61, 0.89), and 0.72 (95% CI: 0.64, 0.88) for wild type, fusion, and V600E, respectively. Conclusion Transfer learning and self-supervised cross-training improved classification performance and generalizability for noninvasive pediatric low-grade glioma mutational status prediction in a limited data scenario. Pediatrics, MRI, CNS, Brain/Brain Stem, Oncology, Feature Detection, Diagnosis, Supervised Learning, Transfer Learning, Convolutional Neural Network (CNN) © RSNA, 2024.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11140508PMC
http://dx.doi.org/10.1148/ryai.230333DOI Listing

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