Revisiting DCE-MRI: Classification of Prostate Tissue Using Descriptive Signal Enhancement Features Derived From DCE-MRI Acquisition With High Spatiotemporal Resolution.


Journal

Investigative radiology
ISSN: 1536-0210
Titre abrégé: Invest Radiol
Pays: United States
ID NLM: 0045377

Informations de publication

Date de publication:
01 09 2021
Historique:
pubmed: 5 3 2021
medline: 16 10 2021
entrez: 4 3 2021
Statut: ppublish

Résumé

A retrospective study (from January 2016 to July 2019) including 75 subjects (mean, 65 years; 46-80 years) with 2.5-second temporal resolution DCE-MRI and PIRADS 4 or 5 lesions was performed. Fifty-four subjects had biopsy-proven prostate cancer (Gleason 6, 15; Gleason 7, 20; Gleason 8, 13; Gleason 9, 6), whereas 21 subjects had negative MRI/ultrasound fusion-guided biopsies. Voxel-wise analysis of contrast signal enhancement was performed for all time points using custom-developed software, including automatic arterial input function detection. Seven descriptive parameter maps were calculated: normalized maximum signal intensity, time to start, time to maximum, time-to-maximum slope, and maximum slope with normalization on maximum signal and the arterial input function (SMN1, SMN2). The parameters were compared with ADC using multiparametric machine-learning models to determine classification accuracy. A Wilcoxon test was used for the hypothesis test and the Spearman coefficient for correlation. There were significant differences (P < 0.05) for all 7 DCE-derived parameters between the normal peripheral zone versus PIRADS 4 or 5 lesions and the biopsy-positive versus biopsy-negative lesions. Multiparametric analysis showed better performance when combining ADC + DCE as input (accuracy/sensitivity/specificity, 97%/93%/100%) relative to ADC alone (accuracy/sensitivity/specificity, 94%/95%/95%) and to DCE alone (accuracy/sensitivity/specificity, 78%/79%/77%) in differentiating the normal peripheral zone from PIRADS lesions, biopsy-positive versus biopsy-negative lesions (accuracy/sensitivity/specificity, 68%/33%/81%), and Gleason 6 versus ≥7 prostate cancer (accuracy/sensitivity/specificity, 69%/60%/72%). Descriptive perfusion characteristics derived from high-resolution DCE-MRI using model-free computations show significant differences between normal and cancerous tissue but do not reach the accuracy achieved with solely ADC-based classification. Combining ADC with DCE-based input features improved classification accuracy for PIRADS lesions, discrimination of biopsy-positive versus biopsy-negative lesions, and differentiation between Gleason 6 versus Gleason ≥7 lesions.

Identifiants

pubmed: 33660631
doi: 10.1097/RLI.0000000000000772
pii: 00004424-202109000-00003
pmc: PMC8373655
mid: NIHMS1707206
doi:

Substances chimiques

Contrast Media 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

553-562

Subventions

Organisme : NIBIB NIH HHS
ID : P41 EB017183
Pays : United States

Informations de copyright

Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest and sources of funding: none declare.

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Auteurs

Hanns C Breit (HC)

From the Department of Radiology, University Hospital Basel, Basel, Switzerland.

Tobias K Block (TK)

NYU Langone Medical Center, New York, NY.

David J Winkel (DJ)

From the Department of Radiology, University Hospital Basel, Basel, Switzerland.

Julian E Gehweiler (JE)

From the Department of Radiology, University Hospital Basel, Basel, Switzerland.

Carl G Glessgen (CG)

From the Department of Radiology, University Hospital Basel, Basel, Switzerland.

Helge Seifert (H)

From the Department of Radiology, University Hospital Basel, Basel, Switzerland.

Christian Wetterauer (C)

From the Department of Radiology, University Hospital Basel, Basel, Switzerland.

Daniel T Boll (DT)

From the Department of Radiology, University Hospital Basel, Basel, Switzerland.

Tobias J Heye (TJ)

From the Department of Radiology, University Hospital Basel, Basel, Switzerland.

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