Weakly-supervised learning-based pathology detection and localization in 3D chest CT scans.

3D pathology localization computed tomography multi‐abnormality detection self‐supervised learning weakly‐supervised learning

Journal

Medical physics
ISSN: 2473-4209
Titre abrégé: Med Phys
Pays: United States
ID NLM: 0425746

Informations de publication

Date de publication:
14 Aug 2024
Historique:
revised: 24 05 2024
received: 11 12 2023
accepted: 01 07 2024
medline: 14 8 2024
pubmed: 14 8 2024
entrez: 14 8 2024
Statut: aheadofprint

Résumé

Recent advancements in anomaly detection have paved the way for novel radiological reading assistance tools that support the identification of findings, aimed at saving time. The clinical adoption of such applications requires a low rate of false positives while maintaining high sensitivity. In light of recent interest and development in multi pathology identification, we present a novel method, based on a recent contrastive self-supervised approach, for multiple chest-related abnormality identification including low lung density area ("LLDA"), consolidation ("CONS"), nodules ("NOD") and interstitial pattern ("IP"). Our approach alerts radiologists about abnormal regions within a computed tomography (CT) scan by providing 3D localization. We introduce a new method for the classification and localization of multiple chest pathologies in 3D Chest CT scans. Our goal is to distinguish four common chest-related abnormalities: "LLDA", "CONS", "NOD", "IP" and "NORMAL". This method is based on a 3D patch-based classifier with a Resnet backbone encoder pretrained leveraging recent contrastive self supervised approach and a fine-tuned classification head. We leverage the SimCLR contrastive framework for pretraining on an unannotated dataset of randomly selected patches and we then fine-tune it on a labeled dataset. During inference, this classifier generates probability maps for each abnormality across the CT volume, which are aggregated to produce a multi-label patient-level prediction. We compare different training strategies, including random initialization, ImageNet weight initialization, frozen SimCLR pretrained weights and fine-tuned SimCLR pretrained weights. Each training strategy is evaluated on a validation set for hyperparameter selection and tested on a test set. Additionally, we explore the fine-tuned SimCLR pretrained classifier for 3D pathology localization and conduct qualitative evaluation. Validated on 111 chest scans for hyperparameter selection and subsequently tested on 251 chest scans with multi-abnormalities, our method achieves an AUROC of 0.931 (95% confidence interval [CI]: [0.9034, 0.9557], The proposed method integrates self-supervised learning algorithms for pretraining, utilizes a patch-based approach for 3D pathology localization and develops an aggregation method for multi-label prediction at patient-level. It shows promise in efficiently detecting and localizing multiple anomalies within a single scan.

Sections du résumé

BACKGROUND BACKGROUND
Recent advancements in anomaly detection have paved the way for novel radiological reading assistance tools that support the identification of findings, aimed at saving time. The clinical adoption of such applications requires a low rate of false positives while maintaining high sensitivity.
PURPOSE OBJECTIVE
In light of recent interest and development in multi pathology identification, we present a novel method, based on a recent contrastive self-supervised approach, for multiple chest-related abnormality identification including low lung density area ("LLDA"), consolidation ("CONS"), nodules ("NOD") and interstitial pattern ("IP"). Our approach alerts radiologists about abnormal regions within a computed tomography (CT) scan by providing 3D localization.
METHODS METHODS
We introduce a new method for the classification and localization of multiple chest pathologies in 3D Chest CT scans. Our goal is to distinguish four common chest-related abnormalities: "LLDA", "CONS", "NOD", "IP" and "NORMAL". This method is based on a 3D patch-based classifier with a Resnet backbone encoder pretrained leveraging recent contrastive self supervised approach and a fine-tuned classification head. We leverage the SimCLR contrastive framework for pretraining on an unannotated dataset of randomly selected patches and we then fine-tune it on a labeled dataset. During inference, this classifier generates probability maps for each abnormality across the CT volume, which are aggregated to produce a multi-label patient-level prediction. We compare different training strategies, including random initialization, ImageNet weight initialization, frozen SimCLR pretrained weights and fine-tuned SimCLR pretrained weights. Each training strategy is evaluated on a validation set for hyperparameter selection and tested on a test set. Additionally, we explore the fine-tuned SimCLR pretrained classifier for 3D pathology localization and conduct qualitative evaluation.
RESULTS RESULTS
Validated on 111 chest scans for hyperparameter selection and subsequently tested on 251 chest scans with multi-abnormalities, our method achieves an AUROC of 0.931 (95% confidence interval [CI]: [0.9034, 0.9557],
CONCLUSIONS CONCLUSIONS
The proposed method integrates self-supervised learning algorithms for pretraining, utilizes a patch-based approach for 3D pathology localization and develops an aggregation method for multi-label prediction at patient-level. It shows promise in efficiently detecting and localizing multiple anomalies within a single scan.

Identifiants

pubmed: 39140793
doi: 10.1002/mp.17302
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 American Association of Physicists in Medicine.

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Auteurs

Aissam Djahnine (A)

CREATIS UMR5220, INSERM U1044, Claude Bernard University Lyon 1, INSA, Lyon, France.
Philips Health Technology innovation, Paris, France.

Emilien Jupin-Delevaux (E)

Department of Radiology, Hospices Civils de Lyon, Lyon, France.

Olivier Nempont (O)

Philips Health Technology innovation, Paris, France.

Salim Aymeric Si-Mohamed (SA)

CREATIS UMR5220, INSERM U1044, Claude Bernard University Lyon 1, INSA, Lyon, France.
Department of Radiology, Hospices Civils de Lyon, Lyon, France.

Fabien Craighero (F)

Department of Radiology, Hospices Civils de Lyon, Lyon, France.

Vincent Cottin (V)

National Reference Center for Rare Pulmonary Diseases, Louis Pradel Hospital, Lyon, France.
Claude Bernard University Lyon 1, Lyon, France.

Philippe Douek (P)

CREATIS UMR5220, INSERM U1044, Claude Bernard University Lyon 1, INSA, Lyon, France.
Department of Radiology, Hospices Civils de Lyon, Lyon, France.

Alexandre Popoff (A)

Philips Health Technology innovation, Paris, France.

Loic Boussel (L)

CREATIS UMR5220, INSERM U1044, Claude Bernard University Lyon 1, INSA, Lyon, France.
Department of Radiology, Hospices Civils de Lyon, Lyon, France.

Classifications MeSH