New parameters of ultrafast dynamic contrast-enhanced breast MRI using compressed sensing.


Journal

Journal of magnetic resonance imaging : JMRI
ISSN: 1522-2586
Titre abrégé: J Magn Reson Imaging
Pays: United States
ID NLM: 9105850

Informations de publication

Date de publication:
01 2020
Historique:
received: 21 03 2019
accepted: 22 05 2019
pubmed: 20 6 2019
medline: 14 4 2021
entrez: 20 6 2019
Statut: ppublish

Résumé

Ultrafast dynamic contrast-enhanced (UF-DCE) breast MRI is considered a promising method of accelerated breast MRI. However, the value of new kinetic parameters derived from UF-DCE need clinical evaluation. To evaluate the diagnostic performance of the maximum slope (MS), time to enhancement (TTE), and time interval between arterial and venous visualization (AVI) derived from UF-DCE MRI using compressed sensing (CS). Retrospective. Seventy-five patients with histologically proven breast lesions. The total number of analyzed lesions was 90 (61 malignant and 29 benign). 3T MRI with UF-DCE MRI based on the 3D gradient-echo volumetric interpolated breath-hold examination (VIBE) sequence using incoherent k-space sampling combined with a CS reconstruction followed by conventional DCE MRI. The diagnostic performance of the MS, TTE, AVI, and conventional kinetic analysis was analyzed and compared with histology. Wilcoxon rank sum test, receiver operating characteristic analysis. The MS was larger and the TTE and AVI were smaller for malignant lesions compared with benign lesions: MS: 29.3%/s and 18.4%/s (P < 0.001), TTE: 7.0 and 12.0 seconds (P < 0.001), AVI: 2.7 and 4.4 frames (P = 0.006) for malignant and benign lesions. The discriminating power of the MS (area under the curve [AUC], 0.76) was slightly better than that of conventional kinetic analysis (AUC, 0.69) and comparable to that of the TTE and AVI (AUC, 0.78 and 0.76 for TTE and AVI, respectively). Invasive lobular carcinoma had smaller MS (21.8%/s) among malignant lesions (29.3%/s). The MS, TTE, and AVI can be used to evaluate breast lesions with clinical performance equivalent to that of conventional kinetic analysis. These parameters vary among histologies. 3 Technical Efficacy: Stage 2 J. Magn. Reson. Imaging 2020;51:164-174.

Sections du résumé

BACKGROUND
Ultrafast dynamic contrast-enhanced (UF-DCE) breast MRI is considered a promising method of accelerated breast MRI. However, the value of new kinetic parameters derived from UF-DCE need clinical evaluation.
PURPOSE
To evaluate the diagnostic performance of the maximum slope (MS), time to enhancement (TTE), and time interval between arterial and venous visualization (AVI) derived from UF-DCE MRI using compressed sensing (CS).
STUDY TYPE
Retrospective.
POPULATION
Seventy-five patients with histologically proven breast lesions. The total number of analyzed lesions was 90 (61 malignant and 29 benign).
FIELD STRENGTH/SEQUENCE
3T MRI with UF-DCE MRI based on the 3D gradient-echo volumetric interpolated breath-hold examination (VIBE) sequence using incoherent k-space sampling combined with a CS reconstruction followed by conventional DCE MRI.
ASSESSMENT
The diagnostic performance of the MS, TTE, AVI, and conventional kinetic analysis was analyzed and compared with histology.
STATISTICAL TESTS
Wilcoxon rank sum test, receiver operating characteristic analysis.
RESULTS
The MS was larger and the TTE and AVI were smaller for malignant lesions compared with benign lesions: MS: 29.3%/s and 18.4%/s (P < 0.001), TTE: 7.0 and 12.0 seconds (P < 0.001), AVI: 2.7 and 4.4 frames (P = 0.006) for malignant and benign lesions. The discriminating power of the MS (area under the curve [AUC], 0.76) was slightly better than that of conventional kinetic analysis (AUC, 0.69) and comparable to that of the TTE and AVI (AUC, 0.78 and 0.76 for TTE and AVI, respectively). Invasive lobular carcinoma had smaller MS (21.8%/s) among malignant lesions (29.3%/s).
DATA CONCLUSION
The MS, TTE, and AVI can be used to evaluate breast lesions with clinical performance equivalent to that of conventional kinetic analysis. These parameters vary among histologies.
LEVEL OF EVIDENCE
3 Technical Efficacy: Stage 2 J. Magn. Reson. Imaging 2020;51:164-174.

Identifiants

pubmed: 31215107
doi: 10.1002/jmri.26838
doi:

Substances chimiques

Contrast Media 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

164-174

Informations de copyright

© 2019 International Society for Magnetic Resonance in Medicine.

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Auteurs

Maya Honda (M)

Department of Diagnostic Imaging and Nuclear Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Masako Kataoka (M)

Department of Diagnostic Imaging and Nuclear Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Natsuko Onishi (N)

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.

Mami Iima (M)

Department of Diagnostic Imaging and Nuclear Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Akane Ohashi (A)

Department of Diagnostic Imaging and Nuclear Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Shotaro Kanao (S)

Department of Diagnostic Radiology, Kobe City Medical Center General Hospital, Kobe, Japan.

Marcel Dominik Nickel (MD)

MR Application Predevelopment, Siemens Healthcare, Erlangen, Germany.

Masakazu Toi (M)

Department of Breast Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Kaori Togashi (K)

Department of Diagnostic Imaging and Nuclear Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.

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