RSS-Feed abonnieren
DOI: 10.1055/a-2643-9818
Automated breast ultrasound features associated with diagnostic performance of Multiview convolutional neural network according to radiologists’ experience
n/aGefördert durch: National Research Foundation of Korea (NRF) grant funded by the Korean government No.2021R1G1A1006474

Purpose: To investigate automated breast ultrasound (ABUS) features affecting the use of Multiview convolutional neural network (CNN) for breast lesions according to radiologists’ experience. Materials and Methods: A total of 656 breast lesions (152 malignant and 504 benign lesions) were included and reviewed by six radiologists for background echotexture, glandular tissue component (GTC), and lesion type and size without as well as with Multiview CNN. The sensitivity, specificity, and the area under the receiver operating curve (AUC) for ABUS features were compared between two sessions according to radiologists’ experience. Results: Radiology residents showed significant AUC improvement with the Multiview CNN for mass (0.81 to 0.91, P=0.003) and non-mass lesions (0.56 to 0.90, P=0.007), all background echotextures (homogeneous-fat: 0.84 to 0.94, P=0.04; homogeneous-fibroglandular: 0.85 to 0.93, P=0.01; heterogeneous: 0.68 to 0.88, P=0.002), all GTC levels (minimal: 0.86 to 0.93, P=0.001; mild: 0.82 to 0.94, P=0.003; moderate: 0.75 to 0.88, P=0.01; marked: 0.68 to 0.89, P<0.001), and lesions ≤10mm (≤5 mm: 0.69 to 0.86, P<0.001; 6–10 mm: 0.83 to 0.92, P<0.001). Breast specialists showed significant AUC improvement with the Multiview CNN in heterogeneous echotexture (0.90 to 0.95, P=0.03), marked GTC (0.88 to 0.95, P<0.001), and lesions ≤10mm (≤5 mm: 0.89 to 0.93, P=0.02; 6–10 mm: 0.95 to 0.98, P=0.01). Conclusion: With the Multiview CNN, the performance of ABUS in radiology residents was improved regardless of lesion type, background echotexture, or GTC. For breast lesions smaller than 10 mm, both radiology residents and breast specialists showed better performance of ABUS.
Publikationsverlauf
Eingereicht: 26. September 2024
Angenommen nach Revision: 26. Juni 2025
Accepted Manuscript online:
26. Juni 2025
© . Thieme. All rights reserved.
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany