Differentiating Well-Differentiated from Poorly-Differentiated HCC: The Potential and the Limitation of Gd-EOB-DTPA in the Presence of Liver Cirrhosis
Andrea Goetz,
Niklas Verloh,
Kirsten Utpatel,
Claudia Fellner,
Janine Rennert,
Ingo Einspieler,
Michael Doppler,
Lukas Luerken,
Leona S. Alizadeh,
Wibke Uller,
Christian Stroszczynski,
Michael Haimerl
Affiliations
Andrea Goetz
Department of Radiology, University Hospital Regensburg, 93053 Regensburg, Germany
Niklas Verloh
Department of Diagnostic and Interventional Radiology, Medical Center University of Freiburg, Faculty of Medicine, University of Freiburg, 79085 Freiburg, Germany
Kirsten Utpatel
Department of Pathology, University Regensburg, 93053 Regensburg, Germany
Claudia Fellner
Department of Radiology, University Hospital Regensburg, 93053 Regensburg, Germany
Janine Rennert
Department of Radiology, University Hospital Regensburg, 93053 Regensburg, Germany
Ingo Einspieler
Department of Radiology, University Hospital Regensburg, 93053 Regensburg, Germany
Michael Doppler
Department of Diagnostic and Interventional Radiology, Medical Center University of Freiburg, Faculty of Medicine, University of Freiburg, 79085 Freiburg, Germany
Lukas Luerken
Department of Radiology, Klinikum Würzburg Mitte, 97074 Würzburg, Germany
Leona S. Alizadeh
Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, 60596 Frankfurt am Main, Germany
Wibke Uller
Department of Diagnostic and Interventional Radiology, Medical Center University of Freiburg, Faculty of Medicine, University of Freiburg, 79085 Freiburg, Germany
Christian Stroszczynski
Department of Radiology, University Hospital Regensburg, 93053 Regensburg, Germany
Michael Haimerl
Department of Radiology, Klinikum Würzburg Mitte, 97074 Würzburg, Germany
This study uses magnetic resonance imaging (MRI) to investigate the potential of the hepatospecific contrast agent gadolinium ethoxybenzyl-diethylenetriaminepentaacetic acid (Gd-EOB-DTPA) in distinguishing G1- from G2/G3-differentiated hepatocellular carcinoma (HCC). Our approach involved analyzing the dynamic behavior of the contrast agent in different phases of imaging by signal intensity (SI) and lesion contrast (C), to surrounding liver parenchyma, and comparing it across distinct groups of patients differentiated based on the histopathological grading of their HCC lesions and the presence of liver cirrhosis. Our results highlighted a significant contrast between well- and poorly-differentiated lesions regarding the lesion contrast in the arterial and late arterial phases. Furthermore, the hepatobiliary phase showed limited diagnostic value in cirrhotic liver parenchyma due to altered pharmacokinetics. Ultimately, our findings underscore the potential of Gd-EOB-DTPA-enhanced MRI as a tool for improving preoperative diagnosis and treatment selection for HCC while emphasizing the need for continued research to overcome the diagnostic complexities posed by the disease.