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Related Experiment Video

Updated: Jan 12, 2026

DTI of the Visual Pathway - White Matter Tracts and Cerebral Lesions
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Image-Based Identification and Localisation of Changes in Intraoperative Brain Tumour Resection.

Adil Jahouh1, Andrei Jalba1, Maxime Chamberland2

  • 1Department of Mathematics and Computer Science, Eindhoven University of Technology, Eindhoven, Netherlands.

Journal of Imaging Informatics in Medicine
|November 7, 2025
PubMed
Summary
This summary is machine-generated.

This study introduces a novel image-based method for tracking brain tumor changes on MRI scans, overcoming issues with inconsistent image acquisition. The approach accurately identifies tumor progression and regression without needing image registration, showing high robustness to real-world imaging variability.

Keywords:
ChangeIntraoperativeResectionSegmentationSiamese networkTumour

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Area of Science:

  • Medical Imaging
  • Artificial Intelligence
  • Neuro-oncology

Background:

  • Conventional methods for tracking brain tumor progression assume consistent MRI scan conditions.
  • Real-world MRI data often exhibit harmonization issues due to variations in acquisition protocols, scanner settings, or patient positioning.
  • These inconsistencies complicate accurate tumor progression assessment.

Purpose of the Study:

  • To develop an image-based approach for identifying and localizing changes between baseline and follow-up MRI scans.
  • To create a method that does not require independent registration or extensive pre-processing.
  • To enhance the tracking of tumor progression and regression in clinical settings with variable imaging quality.

Main Methods:

  • A registration-invariant Siamese network utilizing dilated convolutions to learn long-context spatial features.
  • Directly detecting and localizing changes from input images using learned feature maps.
  • Employing panchromatic sharpening to enhance both high-level structural and pixel-level differences in the change map.

Main Results:

  • The proposed method outperformed baseline models in identifying and localizing resected tumor tissue on unregistered MRI scans (F1=0.64, IoU=0.57 vs. baseline F1=0.11, IoU=0.07).
  • Performance remained robust under augmentation, noise, and misalignment conditions (F1=0.55, IoU=0.45).
  • Demonstrated strong robustness to spatial misalignment, a common issue in clinical MRI.

Conclusions:

  • The developed approach offers a robust solution for tracking brain tumor progression and regression.
  • It effectively addresses harmonization issues and spatial misalignment in MRI data.
  • Presents a promising tool for clinical environments where reliable image registration is not always feasible.