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Evaluation of Remnant Liver Function Using Primovist-enhanced MRI Before Resection/Ablation of Hepatocellular Carcinoma

Pre-Surgical Treatment or Radio Frequency Ablation (RFA) Evaluation of Future Remnant Liver Function Using Gd-EOB-DTPA Enhanced MRI in Patients Undergoing Hepatic Resection /RFA for Hepatocellular Carcinoma

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01490203
Acronym
LiFE
Enrollment
71
Registered
2011-12-12
Start date
2011-12-31
Completion date
2016-12-31
Last updated
2018-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carcinoma, Hepatocellular, Liver Dysfunction

Keywords

Gd-EOB-DTPA, MRI, Hepatectomy, Hepatocellular Carcinoma, Liver Function Tests

Brief summary

The purpose of this study is to determine whether the global and segmental hepatic uptake and excretion of Gd-EOB-DTPA on Gd-EOB-DTPA-enhanced liver MRI correlates with standard liver function test results in the patients with Hepatocellular Carcinoma (HCC) before major hepatic resection or radiofrequency ablation (RFA).

Detailed description

1. Preoperative/RFA assessment of remnant liver function is important for avoiding posthepatectomy liver failure. However, the function of the future remnant is decreased in patients with chronic liver disease or cirrhosis, compared to that of healthy patients with an equal volume. Therefore, volume-based estimation of hepatic reserve function is inadequate for patients with hepatic dysfunction. 2. Standard clinical liver function tests, such as ICG clearance rate or Child-Pugh score, provides measurements of the global hepatic function, but cannot evaluate the functional distribution in the liver. Gd-EOB-DTPA (Gadoxetic acid, Primovist®, Bayer Schering) enhanced MRI has been recently demonstrated to have the potential to be an imaging-based liver function test, with the possibility to detect functional differences on a regional or even segmental level. 3. Gd-EOB-DTPA-enhanced liver MRI may be able to assess not only global but also segmental liver function in patients with hepatocellular carcinoma (HCC) who have a relatively high risk for developing liver failure after surgical resection due to coexistent hepatic damage by chronic viral hepatitis and/or cirrhosis preoperatively. The purpose of this study is to determine whether the global and segmental hepatic uptake and excretion of Gd-EOB-DTPA on Gd-EOB-DTPA-enhanced liver MRI correlates with standard liver function test results in the patients with HCC before major hepatic resection/RFA.

Interventions

DRUGGd-EOB-DTPA

1. Gd-EOB-DTPA enhanced MRI will be obtained within 1 week before, and within 3 to 5 days after surgical resection of the liver. 2. Gd-EOB-DTPA will be administered intravenously with an amount of 0.1mL/kg, 1mL/sec injection rate, followed by saline infusion.

PROCEDUREMRI

1. Gd-EOB-DTPA enhanced MRI will be obtained within 1 week before, and within 3 to 5 days after surgical resection of the liver. 2. Multiphasic MRI including dynamic hepatocyte specific phase will be performed for evaluation of hepatic extraction fraction, with 25 phase dynamic MRI obtained until 30 minutes after contrast injection.

Sponsors

Bayer
CollaboratorINDUSTRY
Seoul St. Mary's Hospital
CollaboratorOTHER
Asan Medical Center
CollaboratorOTHER
Chonnam National University Hospital
CollaboratorOTHER
Seoul National University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Patients with the diagnosis of HCC based on noninvasive diagnostic criteria of HCC proposed by 2010 AASLD 2. Surgical resection of hepatic resection greater than 2 Couinaud segments (including total hepatectomy for transplantation) or radiofrequency ablation is planned 3. Patients who provided the informed consent

Exclusion criteria

1. Patients younger than 18 yrs old 2. Patients who received hepatic surgery prior to this study 3. Patients who underwent TACE or RFA for greater than 2 segments within 3 months prior to this study 4. Patients who received radiation treatment including the liver or systemic chemotherapy 5. Patients who underwent contrast enhanced liver MRI within 3 days prior to this study 6. Patients with severe renal dysfunction (Cr .2.5 mg/dL or GFR \< 30mL/min) 7. Patients with hypersensitivity to gadolinium 8. Patients with uncorrectable hypokalemia 9. Pregnant women, or reproductive age women who will not agree with contraception during this study period. 10. Patients with mental disorder which will interfere with voluntary agreement 11. Patients who have any contraindication to MRI (cardiac pacemaker, ferromagnetic implants, etc.) 12. Any other condition which, in the opinion of the Investigator, would make the patient unsuitable for enrollment or could interfere with the completion of the study.

Design outcomes

Primary

MeasureTime frameDescription
Correlation of hepatic extraction fraction (HEF) of future remnant liver function (RLF) obtained from Gd-EOB-DTPA enhanced MRI with postoperative ICG R15 clearance test results3 days (upto 5 days) after surgeryPredicted RLF (HEF mL) = the sum of the individual HEF of each voxel in future remnant segment

Secondary

MeasureTime frameDescription
Correlation of various functional and volumetric parameters derived from Gd-EOB-DTPA enhanced MRI and clinical liver function tests obtained before and after surgical resectionwithin 7 days before, and 3 to 5 days after surgery1. Functional parameters derived from Gd-EOB-DTPA enhanced MRI include hepatic extraction fraction \[HEF\], input-relative blood flow \[irBF\], hepatocellular uptake index \[HUI\], liver to spleen ratio (LSR). 2. Volumetric parameters include global liver volume and remnant liver volume. 3. Clinical liver function tests include ICG R15, MELD score and Child-Pugh score. 4. ICG R15 \[Indocyanine green retention at 15 minutes, %\] test will be performed within 3 days of preoperative MRI and 3 days after surgical resection.
Analysis of clinical and MRI parameters of postoperative complication and morbidityupto 3 months (plus minus 1 week) after discharge1. Clinical parameters refer to the following. * Frequency of POD#5 days 50-50 criteria * Evaluation of operation related complication * Incidence of hepatic failure or death 2. Functional and volumetric MRI parameters of patients with postoperative complication and morbidity will be evaluated. 3. Correlation of MRI parameters with laboratory liver function tests.
Exploratory analysis of MRI parameters and ICG R15 derived from potential liver donorswithin 3 days of ICG R15 test1. Correlation of functional parameters derived from Gd-EOB-DTPA enhanced MRI with ICG R15 2. Correlation of functional and volumetric parameters derived from Gd-EOB-DTPA enhanced MRI 3. Correlation of volumetric parameters derived from Gd-EOB-DTPA enhanced MRI and ICG15 4. Comparison of functional MRI parameters between potential liver donors and patients undergoing hepatic resection for HCC.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026