Gadoxetic Acid-enhanced MR Evaluation of Hepatocellular Carcinoma and Dysplastic Nodules in the Cirrhotic Liver (PriMPa)

Jae Ho Byun

Status: Withdrawn

Conditions: Carcinoma, Hepatocellular; Liver Cirrhosis

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT01501240

AMC-2011-0797

Details and patient eligibility

About

A prospective intra-individual study to investigate the diagnostic performance of gadoxetic acid-enhanced MR for the patients with liver cirrhosis using thin-section whole-explant as standard of reference

Full description

Liver cirrhosis is a progressive, diffuse disease of the liver characterized by hepatocyte necrosis, fibrosis, distortion of the normal hepatic architecture and a spectrum of nodular lesions that includes regenerative nodules (RN), dysplastic nodules (DN) and hepatocellular carcinomas (HCC). Since HCC is the leading cause of death among the patients with liver cirrhosis, Early and accurate diagnosis of HCC and its precursors by using optimal imaging technique is critical for its treatment and management.

Recently state-of-the-art magnetic resonance (MR) imaging with gadoxetic acid, which works both an extracellular and hepatocyte-specific contrast agent, has been increasing used to evaluate the patients with liver cirrhosis. Several studies correlated gadoxetic acid-enhanced MR of HCC and hepatocellular nodules with the pathology from biopsy or surgical resection specimens. However, all of those studies are limited by its lack of complete correlation between pathologic and imaging findings and the resulting bias being toward the positive studies. Ideally, the use of whole explant pathologic correlation would be helpful for exact characterization of HCC and its precursors on gadoxetic acid-enhanced MR.

The question of our study is how accurate gadoxetic acid-enhanced MR is in the evaluation of the patients with cirrhotic liver to detect HCC and dysplastic nodules and, by using thin-section whole-explant correlation following liver transplantation as the reference standard.

Sex: All

Ages: 20 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with known liver cirrhosis based on either histology, or a combination of physical examination, laboratory tests, and imaging data
• Patients with known liver cirrhosis based on either histology, or a combination of physical examination, laboratory tests, and imaging data

Exclusion criteria

• Patients under 20 years of age
• Patients who have more than 10 nodules detected on hepatobiliary phase of gadoxetic acid-enhanced MR
• Patients who underwent transarterial chemotherapy or radiofrequency ablation
• Women who are pregnant, lactating or who are of childbearing potential
• Patients with any physical or mental status than interferes with the signing of informed consent
• Patients with a contraindication for MR
• Patients with impaired renal function (e.g. acute renal failure or eGFR < 30 ml/min/1.73m2) or patients on dialysis

Trial design

0 participants in 1 patient group

liver cirrhosis, liver transplantation

Description:

Patients with known liver cirrhosis and planned to undergo liver transplantation within 1 month will be eligible population in the study