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Interinstitutional Portability of a Deep Learning Brain MRI Lesion Segmentation Algorithm.

Andreas M Rauschecker1, Tyler J Gleason1, Pierre Nedelec1

  • 1Department of Radiology & Biomedical Imaging, University of California, San Francisco, 513 Parnassus Ave, Room S-261, Box 0628, San Francisco, CA 94143-0628 (A.M.R., T.J.G., P.N., D.A.W., E.C., J.B.C., L.P.S., J.D.R., C.P.H.); and Department of Radiology, Hospital of the University of Pennsylvania, Philadelphia, Pa (M.T.D., D.W.).

Radiology. Artificial Intelligence
|February 11, 2022
PubMed
Summary
This summary is machine-generated.

Adding relevant external brain MRI data improved lesion segmentation performance. A small amount of diverse data from a new institution significantly boosted algorithm accuracy, enabling successful application across different sites.

Keywords:
Brain/Brain StemNeural NetworksSegmentation

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Area of Science:

  • Artificial Intelligence in Medical Imaging
  • Machine Learning for Neuroscience
  • Radiology and Diagnostic Imaging

Background:

  • Brain MRI lesion segmentation algorithms are crucial for diagnosis and treatment planning.
  • Performance of algorithms trained at one institution often degrades when applied to data from another due to variations in imaging protocols and patient populations.
  • Multi-institutional training datasets are explored to enhance algorithm generalizability.

Purpose of the Study:

  • To evaluate the performance of a brain MRI lesion segmentation algorithm trained at one institution (IN1) when tested at a second institution (IN2).
  • To assess the impact of incorporating multi-institutional training data on mitigating performance decline in external validation.
  • To determine the optimal strategy for augmenting training datasets to improve cross-institutional generalizability.

Main Methods:

  • A 3D U-Net model was initially trained on 293 brain MRI scans from IN1 and tested on 51 scans from IN2.
  • The model was subsequently retrained with additional datasets: 285 multi-institution tumor segmentations, 198 IN2 tumor segmentations, and 34 IN2 heterogeneous lesion segmentations.
  • Segmentation performance was quantified using Dice coefficients on both IN1 and IN2 test datasets.

Main Results:

  • The algorithm demonstrated accurate segmentation across various brain pathologies but showed reduced performance on external data (median Dice score 0.70 for IN2 vs. 0.76 for IN1).
  • Adding 483 cases of a single pathology, even from IN2, did not significantly improve external performance (median Dice 0.72, P = .10).
  • Incorporating a small subset (34 cases) of diverse IN2 lesion data (10% of total training data) significantly improved performance to baseline levels (Dice score 0.77, P < .001), with high correlation (Spearman r = 0.98) in total lesion volumes.

Conclusions:

  • A modest addition of relevant, heterogeneous training data from an external institution can successfully adapt a pre-trained brain MRI segmentation model for use at that new site.
  • The findings highlight the importance of data diversity over sheer volume when augmenting training sets for improved cross-institutional performance.
  • This approach facilitates the reliable application of AI models in diverse clinical settings, enhancing diagnostic capabilities.