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Research ArticleAdult Brain
Open Access

Unsupervised Deep Learning for Stroke Lesion Segmentation on Follow-up CT Based on Generative Adversarial Networks

H. van Voorst, P.R. Konduri, L.M. van Poppel, W. van der Steen, P.M. van der Sluijs, E.M.H. Slot, B.J. Emmer, W.H. van Zwam, Y.B.W.E.M. Roos, C.B.L.M. Majoie, G. Zaharchuk, M.W.A. Caan and H.A. Marquering on behalf of the CONTRAST Consortium Collaborators
American Journal of Neuroradiology August 2022, 43 (8) 1107-1114; DOI: https://doi.org/10.3174/ajnr.A7582
H. van Voorst
aFrom the Departments of Radiology and Nuclear Medicine (H.v.V., P.R.K., L.M.v.P., B.J.E., C.B.L.M.M., H.A.M.)
bBiomedical Engineering and Physics (H.v.V., P.R.K., L.M.v.P., M.W.A.C., H.A.M.)
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P.R. Konduri
aFrom the Departments of Radiology and Nuclear Medicine (H.v.V., P.R.K., L.M.v.P., B.J.E., C.B.L.M.M., H.A.M.)
bBiomedical Engineering and Physics (H.v.V., P.R.K., L.M.v.P., M.W.A.C., H.A.M.)
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L.M. van Poppel
aFrom the Departments of Radiology and Nuclear Medicine (H.v.V., P.R.K., L.M.v.P., B.J.E., C.B.L.M.M., H.A.M.)
bBiomedical Engineering and Physics (H.v.V., P.R.K., L.M.v.P., M.W.A.C., H.A.M.)
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W. van der Steen
dDepartments of Neurology (W.v.d.S., P.M.v.d.S.)
eRadiology and Nuclear Medicine (W.v.d.S., P.M.v.d.S.), Erasmus University Medical Center, Rotterdam, the Netherlands
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P.M. van der Sluijs
dDepartments of Neurology (W.v.d.S., P.M.v.d.S.)
eRadiology and Nuclear Medicine (W.v.d.S., P.M.v.d.S.), Erasmus University Medical Center, Rotterdam, the Netherlands
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E.M.H. Slot
fDepartment of Neurology and Neurosurgery (E.M.H.S.), University Medical Center Utrecht, Utrecht, the Netherlands
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B.J. Emmer
aFrom the Departments of Radiology and Nuclear Medicine (H.v.V., P.R.K., L.M.v.P., B.J.E., C.B.L.M.M., H.A.M.)
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W.H. van Zwam
gDepartment of Radiology and Nuclear Medicine (W.H.v.Z.), Maastricht University Medical Center, Maastricht, the Netherlands
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Y.B.W.E.M. Roos
cNeurology (Y.B.W.E.M.R.), Faculty of Medicine, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands
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C.B.L.M. Majoie
aFrom the Departments of Radiology and Nuclear Medicine (H.v.V., P.R.K., L.M.v.P., B.J.E., C.B.L.M.M., H.A.M.)
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G. Zaharchuk
hDepartment of Radiology (G.Z.), Stanford University, Stanford, California
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M.W.A. Caan
bBiomedical Engineering and Physics (H.v.V., P.R.K., L.M.v.P., M.W.A.C., H.A.M.)
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H.A. Marquering
aFrom the Departments of Radiology and Nuclear Medicine (H.v.V., P.R.K., L.M.v.P., B.J.E., C.B.L.M.M., H.A.M.)
bBiomedical Engineering and Physics (H.v.V., P.R.K., L.M.v.P., M.W.A.C., H.A.M.)
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Abstract

BACKGROUND AND PURPOSE: Supervised deep learning is the state-of-the-art method for stroke lesion segmentation on NCCT. Supervised methods require manual lesion annotations for model development, while unsupervised deep learning methods such as generative adversarial networks do not. The aim of this study was to develop and evaluate a generative adversarial network to segment infarct and hemorrhagic stroke lesions on follow-up NCCT scans.

MATERIALS AND METHODS: Training data consisted of 820 patients with baseline and follow-up NCCT from 3 Dutch acute ischemic stroke trials. A generative adversarial network was optimized to transform a follow-up scan with a lesion to a generated baseline scan without a lesion by generating a difference map that was subtracted from the follow-up scan. The generated difference map was used to automatically extract lesion segmentations. Segmentation of primary hemorrhagic lesions, hemorrhagic transformation of ischemic stroke, and 24-hour and 1-week follow-up infarct lesions were evaluated relative to expert annotations with the Dice similarity coefficient, Bland-Altman analysis, and intraclass correlation coefficient.

RESULTS: The median Dice similarity coefficient was 0.31 (interquartile range, 0.08–0.59) and 0.59 (interquartile range, 0.29–0.74) for the 24-hour and 1-week infarct lesions, respectively. A much lower Dice similarity coefficient was measured for hemorrhagic transformation (median, 0.02; interquartile range, 0–0.14) and primary hemorrhage lesions (median, 0.08; interquartile range, 0.01–0.35). Predicted lesion volume and the intraclass correlation coefficient were good for the 24-hour (bias, 3 mL; limits of agreement, −64−59 mL; intraclass correlation coefficient, 0.83; 95% CI, 0.78–0.88) and excellent for the 1-week (bias, −4 m; limits of agreement,−66−58 mL; intraclass correlation coefficient, 0.90; 95% CI, 0.83–0.93) follow-up infarct lesions.

CONCLUSIONS: An unsupervised generative adversarial network can be used to obtain automated infarct lesion segmentations with a moderate Dice similarity coefficient and good volumetric correspondence.

ABBREVIATIONS:

AIS
acute ischemic stroke
BL
baseline
DSC
Dice similarity coefficient
FU
follow-up
FU2BL-GAN
follow-up to baseline generative adversarial network
GAN
generative adversarial network
24H
24 hours
HT
hemorrhagic transformation
ICC
intraclass correlation coefficient
IQR
interquartile range
L1-loss
voxelwise absolute difference between generated baseline and real baseline NCCTs
L1+adv
L1 and adversarial loss
LoA
limits of agreement
nnUnet
no new Unet
PrH
primary hemorrhagic lesions
1W
1 week
  • © 2022 by American Journal of Neuroradiology

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H. van Voorst, P.R. Konduri, L.M. van Poppel, W. van der Steen, P.M. van der Sluijs, E.M.H. Slot, B.J. Emmer, W.H. van Zwam, Y.B.W.E.M. Roos, C.B.L.M. Majoie, G. Zaharchuk, M.W.A. Caan, H.A. Marquering
Unsupervised Deep Learning for Stroke Lesion Segmentation on Follow-up CT Based on Generative Adversarial Networks
American Journal of Neuroradiology Aug 2022, 43 (8) 1107-1114; DOI: 10.3174/ajnr.A7582

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Unsupervised DL for Stroke Lesion Segmentation
H. van Voorst, P.R. Konduri, L.M. van Poppel, W. van der Steen, P.M. van der Sluijs, E.M.H. Slot, B.J. Emmer, W.H. van Zwam, Y.B.W.E.M. Roos, C.B.L.M. Majoie, G. Zaharchuk, M.W.A. Caan, H.A. Marquering
American Journal of Neuroradiology Aug 2022, 43 (8) 1107-1114; DOI: 10.3174/ajnr.A7582
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