Liver Imaging Reporting and Data System Contrast-Enhanced US Nonradiation Treatment Response Assessment Version 2024
Andrej Lyshchik1, David T Fetzer1, Yuko Kono1
1From the Department of Radiology, Thomas Jefferson University Hospital, 132 S 10th St, 763G Main Bldg, Philadelphia, PA 19107 (A.L.); Department of Radiology, UT Southwestern Medical Center, Dallas, Tex (D.T.F.); Departments of Medicine and Radiology, University of California, San Diego, San Diego, Calif (Y.K.); Department of Diagnostic Imaging, University of Calgary, Calgary, Alberta, Canada (S.R.W.); Department of General Internal Medicine, Hirslanden Klinik Beau-Site, Hirslanden Salem-Spital, and Hirslanden Klinik Permanence, Bern, Switzerland (C.F.D.); Interdisciplinary Ultrasound Center, Department of Radiology, LMU University Hospital, Ludwig Maximilian University of Munich, Munich, Germany (D.A.C.); Department of Interventional Ultrasound, Casa di Cura Igea, Milan, Italy (M.F.M.); Joint Department of Medical Imaging, University of Toronto, Toronto, Ontario, Canada (H.J.J., T.K.K.); Department of Radiology and Institute of Radiation Medicine, Seoul National University Hospital, Seoul, Korea (J.M.L.); Department of Radiology, Seoul National University College of Medicine, Seoul, Korea (J.M.L.); Department of Gastroenterology and Hepatology, Faculty of Medicine, Kindai University, Osaka, Japan (Y.M., M.K.); Hepatobiliary and Immunoallergic Diseases, Division of Internal Medicine, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy (F.P.); and Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy (F.P.).
None:
The American College of Radiology Liver Imaging Reporting and Data System (LI-RADS) standardizes the imaging technique, reporting lexicon, disease categorization, and management for patients with or at risk for hepatocellular carcinoma (HCC). LI-RADS encompasses HCC surveillance with US; HCC diagnosis with CT, MRI, or contrast-enhanced US (CEUS); and treatment response assessment (TRA) with CT or MRI. LI-RADS was recently expanded to include CEUS TRA after nonradiation locoregional therapy or surgical resection. This report provides an overview of LI-RADS CEUS Nonradiation TRA v2024, including a lexicon of imaging findings, techniques, and imaging criteria for posttreatment tumor viability assessment. LI-RADS CEUS Nonradiation TRA v2024 takes into consideration differences in the CEUS appearance of viable tumor and posttreatment changes within and in close proximity to a treated lesion. Due to the high sensitivity of CEUS to vascular flow, posttreatment reactive changes commonly manifest as areas of abnormal perilesional enhancement without washout, especially in the first 3 months after treatment. To improve the accuracy of CEUS for nonradiation TRA, different diagnostic criteria are used to evaluate tumor viability within and outside of the treated lesion margin. Broader criteria for intralesional enhancement increase sensitivity for tumor viability detection. Stricter criteria for perilesional enhancement limit miscategorization of posttreatment reactive changes as viable tumor. Finally, the TRA algorithm reconciles intralesional and perilesional tumor viability assessment and assigns a single LI-RADS treatment response (LR-TR) category: LR-TR nonviable, LR-TR equivocal, or LR-TR viable.
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