Association between real-time shear wave elastography findings and HER-2 expression in breast cancer

  • 0Department of Ultrasound Medicine, The Affiliated People's Hospital of Ningbo University, Ningbo, China.

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Summary

This summary is machine-generated.

Shear wave elastography (SWE) shows potential for assessing Human Epidermal growth factor Receptor-2 (HER-2) status in breast cancer. The maximum elastic modulus (Emax) combined with lesion size and calcification demonstrated moderate accuracy in predicting HER-2 positivity.

Area Of Science

  • Medical Imaging
  • Oncology
  • Biophysics

Background

  • Human Epidermal growth factor Receptor-2 (HER-2) positive breast cancer exhibits aggressive traits and poorer outcomes.
  • Accurate HER-2 status determination is crucial for effective breast cancer treatment planning.
  • Real-time shear wave elastography (SWE) is explored as a non-invasive method to assess HER-2 expression.

Purpose Of The Study

  • To investigate the correlation between real-time shear wave elastography (SWE) parameters and HER-2 expression levels in breast cancer.
  • To evaluate the diagnostic performance of SWE in differentiating HER-2 positive from HER-2 negative breast cancer lesions.

Main Methods

  • Retrospective analysis of 67 patients with 70 breast cancer lesions (31 HER-2 negative, 39 HER-2 positive).
  • Shear wave elastography (SWE) measurements including mean (Emean), maximum (Emax), and minimum (Emin) elastic modulus.
  • Receiver operating characteristic (ROC) curve analysis to assess diagnostic efficacy for HER-2 positivity.

Main Results

  • HER-2 positive lesions were more frequently larger than 20 mm.
  • A significantly lower Emax value was observed in the HER-2 positive group (P<0.05).
  • The combination of Emax, lesion size, and calcification yielded the highest Area Under the Curve (AUC) of 0.800, with 66.7% sensitivity and 83.9% specificity.

Conclusions

  • Emax, lesion size, and calcification show a moderate association with HER-2 positivity.
  • SWE, particularly Emax, may serve as a valuable non-invasive tool to complement existing methods for assessing HER-2 status in breast cancer.