4.6 Article

Improved Breast 2D SWE Algorithm to Eliminate False-Negative Cases

Journal

INVESTIGATIVE RADIOLOGY
Volume 58, Issue 10, Pages 703-709

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/RLI.0000000000000972

Keywords

breast cancer; BI-RADS; elastography; shear wave; strain elastography; false-negative cancers

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This study evaluated a new breast 2D-SWE algorithm and compared it with the standard algorithm. The results showed that the new algorithm significantly improved the sensitivity of the technique with a small decrease in specificity, thus improving the characterization of breast lesions.
Objectives: Two-dimensional shear wave elastography (SWE) has been limited in breast lesion characterization due to false-negative results from artifacts. The aim of this study was to evaluate an updated Food and Drug Administration-approved breast 2D-SWE algorithm and compare with the standard algorithm (SA). Materials and Methods: This prospective, single-center study was approved by our local institutional review board and Health Insurance Portability and Accountability Act compliant. From April 25, 2019 to May 2, 2022, raw shear wave data were saved on patients having screening or diagnostic breast ultrasound on a Siemens Sequoia US. After removing duplicate images and those without biopsy diagnosis or stability over 2 years, there were 298 patients with 394 lesions with biopsy-proven pathology or >2-year follow-up. Raw data were processed using the SA and a new algorithm (NA). Five-millimeter regions of interestwere placed in the highest stiffness in the lesion or adjacent 3 mm on the SA. Stiffness values (shear wave speed, max) in this location from both algorithms were recorded. Statistics were calculated for comparing the 2 algorithms. Results: The mean patient age was 56.3 +/- 16.1 years (range, 21-93 years). The mean benign lesion sizewas 10.7 +/- 8.0 mm (range, 2-46mm), whereas the mean malignant lesion size was 14.9 +/- 7.8 mm (range, 4-36 mm). There were 201 benign (>2-year follow-up) and 193 biopsied lesions (65 benign; 128 malignant). The mean maximum stiffness for benign lesions was 2.37 m/s (SD 1.26 m/s) for SA and 3.51 m/s (SD 2.05 m/s) for NA. For malignant lesions, the mean maximum stiffness was 4.73 m/s (SD, 1.71 m/s) for SA and 8.45 m/s (SD, 1.42 m/s) for NA. The area under the receiver operating characteristic curve was 0.87 SA and 0.95 NAwhen using the optimal cutoff value. Using a threshold value of 5.0m/s for NA and comparing to SA, the sensitivity increased from 0.45 to 1.00 and the specificity decreased from 0.94 to 0.81; the positive predictive value was 0.72, the negative predictive value was 1.00, and the negative likelihood ratio was 0.00. Conclusions: Using a new breast SWE algorithm significantly improves the sensitivity of the technique with a small decrease in specificity, virtually eliminating the soft cancer artifact. The new 2D-SWE algorithm significantly increases the sensitivity and negative predictive value in characterizing breast lesions as benign or malignant and allows for downgrading all BI-RADS 4 lesions.

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