AI Article Synopsis

  • The study focuses on creating an automated system for measuring tumor sizes in pediatric brain tumors using MRI imagery, which is important for assessing treatment responses.
  • A deep learning model, specifically a 3D U-Net, was trained on a large dataset to perform tumor segmentation and size measurement, and its results were compared with those of expert human raters.
  • The findings show strong agreement between the automated system and manual assessments, suggesting that the tool could enhance accuracy and efficiency in monitoring tumor response in pediatric patients, though further validation is needed.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804897PMC
http://dx.doi.org/10.1093/neuonc/noab151DOI Listing

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