PERSoN4: A multiparametric ultrasound model to improve CEUS LI-RADS for HCC

Esposto Giorgio1, Santini Paolo2, Galasso Linda1

  • 1CEMAD Digestive Disease Center, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Università Cattolica del Sacro Cuore di Roma, Rome, Italy.

Insights

A new model, PERSoN4, enhances Dynamic Contrast-Enhanced Ultrasound (D-CEUS) for diagnosing hepatocellular carcinoma (HCC). This tool could enable non-invasive HCC diagnosis in nearly 50% of patients, reducing the need for liver biopsies.

Area of Science:

  • Hepatology and Radiology
  • Medical Imaging and Diagnostics
  • Oncology

Background:

  • Accurate non-invasive diagnosis of hepatocellular carcinoma (HCC) is challenging, especially with atypical vascular patterns on Dynamic Contrast-Enhanced Ultrasound (D-CEUS).
  • Developing multiparametric D-CEUS risk models integrating quantitative perfusion analysis with clinical and imaging features is crucial.

Purpose of the Study:

  • To evaluate the diagnostic performance of a novel multiparametric D-CEUS-based risk model (PERSoN4) for non-invasive HCC diagnosis.
  • To assess the model's ability to improve upon existing CEUS LI-RADS criteria.

Main Methods:

  • A cohort study enrolled 88 patients with chronic liver disease undergoing liver biopsy.
  • CEUS was performed, and data were analyzed using logistic regression to develop the PERSoN4 model, incorporating clinical and imaging variables.
  • The model's accuracy was validated on an independent cohort.

Main Results:

  • The PERSoN4 model, including variables like sex, nodule count, rim-like hyperenhancement, and Peak Enhancement ratio, showed high accuracy (AUC 0.91) in the training cohort.
  • In the validation cohort, the model achieved 48.8% sensitivity, 100.0% specificity, and 100.0% positive predictive value (PPV), with an AUC of 0.74.

Conclusions:

  • The PERSoN4 model shows potential to significantly improve CEUS LI-RADS performance for HCC diagnosis.
  • This approach could reduce liver biopsy needs by nearly 50% in eligible patients, though further external validation is required.
Abstract