Combined model-based and deep learning-based automated 3D zonal segmentation of the prostate on T2-weighted MR images: clinical evaluation.


Journal

European radiology
ISSN: 1432-1084
Titre abrégé: Eur Radiol
Pays: Germany
ID NLM: 9114774

Informations de publication

Date de publication:
May 2022
Historique:
received: 06 08 2021
accepted: 09 10 2021
revised: 28 09 2021
pubmed: 11 1 2022
medline: 28 4 2022
entrez: 10 1 2022
Statut: ppublish

Résumé

To train and to test for prostate zonal segmentation an existing algorithm already trained for whole-gland segmentation. The algorithm, combining model-based and deep learning-based approaches, was trained for zonal segmentation using the NCI-ISBI-2013 dataset and 70 T2-weighted datasets acquired at an academic centre. Test datasets were randomly selected among examinations performed at this centre on one of two scanners (General Electric, 1.5 T; Philips, 3 T) not used for training. Automated segmentations were corrected by two independent radiologists. When segmentation was initiated outside the prostate, images were cropped and segmentation repeated. Factors influencing the algorithm's mean Dice similarity coefficient (DSC) and its precision were assessed using beta regression. Eighty-two test datasets were selected; one was excluded. In 13/81 datasets, segmentation started outside the prostate, but zonal segmentation was possible after image cropping. Depending on the radiologist chosen as reference, algorithm's median DSCs were 96.4/97.4%, 91.8/93.0% and 79.9/89.6% for whole-gland, central gland and anterior fibromuscular stroma (AFMS) segmentations, respectively. DSCs comparing radiologists' delineations were 95.8%, 93.6% and 81.7%, respectively. For all segmentation tasks, the scanner used for imaging significantly influenced the mean DSC and its precision, and the mean DSC was significantly lower in cases with initial segmentation outside the prostate. For central gland segmentation, the mean DSC was also significantly lower in larger prostates. The radiologist chosen as reference had no significant impact, except for AFMS segmentation. The algorithm performance fell within the range of inter-reader variability but remained significantly impacted by the scanner used for imaging. • Median Dice similarity coefficients obtained by the algorithm fell within human inter-reader variability for the three segmentation tasks (whole gland, central gland, anterior fibromuscular stroma). • The scanner used for imaging significantly impacted the performance of the automated segmentation for the three segmentation tasks. • The performance of the automated segmentation of the anterior fibromuscular stroma was highly variable across patients and showed also high variability across the two radiologists.

Identifiants

pubmed: 35001157
doi: 10.1007/s00330-021-08408-5
pii: 10.1007/s00330-021-08408-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3248-3259

Informations de copyright

© 2021. The Author(s), under exclusive licence to European Society of Radiology.

Références

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Auteurs

Olivier Rouvière (O)

Department of Urinary and Vascular Imaging, Hôpital Edouard Herriot, Hospices Civils de Lyon, Pavillon B, 5 place d'Arsonval, F-69437, Lyon, France. olivier.rouviere@netcourrier.com.
Université de Lyon, F-69003, Lyon, France. olivier.rouviere@netcourrier.com.
Faculté de Médecine Lyon Est, Université Lyon 1, F-69003, Lyon, France. olivier.rouviere@netcourrier.com.
INSERM, LabTau, U1032, Lyon, France. olivier.rouviere@netcourrier.com.

Paul Cezar Moldovan (PC)

Department of Urinary and Vascular Imaging, Hôpital Edouard Herriot, Hospices Civils de Lyon, Pavillon B, 5 place d'Arsonval, F-69437, Lyon, France.

Anna Vlachomitrou (A)

Philips France, 33 rue de Verdun, CS 60 055, 92156, Suresnes Cedex, France.

Sylvain Gouttard (S)

Department of Urinary and Vascular Imaging, Hôpital Edouard Herriot, Hospices Civils de Lyon, Pavillon B, 5 place d'Arsonval, F-69437, Lyon, France.

Benjamin Riche (B)

Service de Biostatistique Et Bioinformatique, Pôle Santé Publique, Hospices Civils de Lyon, F-69003, Lyon, France.
Laboratoire de Biométrie Et Biologie Évolutive, Équipe Biostatistique-Santé, UMR 5558, CNRS, F-69100, Villeurbanne, France.

Alexandra Groth (A)

Philips Research, Röntgenstrasse 24-26, 22335, Hamburg, Germany.

Mark Rabotnikov (M)

Philips, MATAM Industrial Park, 3508409, Haifa, Israel.

Alain Ruffion (A)

Department of Urology, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, F-69310, Pierre-Bénite, France.

Marc Colombel (M)

Université de Lyon, F-69003, Lyon, France.
Faculté de Médecine Lyon Est, Université Lyon 1, F-69003, Lyon, France.
Department of Urology, Hôpital Edouard Herriot, Hospices Civils de Lyon, F-69437, Lyon, France.

Sébastien Crouzet (S)

Department of Urology, Hôpital Edouard Herriot, Hospices Civils de Lyon, F-69437, Lyon, France.

Juergen Weese (J)

Philips Research, Röntgenstrasse 24-26, 22335, Hamburg, Germany.

Muriel Rabilloud (M)

Université de Lyon, F-69003, Lyon, France.
Faculté de Médecine Lyon Est, Université Lyon 1, F-69003, Lyon, France.
Service de Biostatistique Et Bioinformatique, Pôle Santé Publique, Hospices Civils de Lyon, F-69003, Lyon, France.
Laboratoire de Biométrie Et Biologie Évolutive, Équipe Biostatistique-Santé, UMR 5558, CNRS, F-69100, Villeurbanne, France.

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