Assessment of Remnant Liver Function in ALPPS by Gd-EOB-DTPA Enhanced MRI

Liver Malignant Tumors Clinical Trial

Official title:

Assessment of Remnant Liver Function in ALPPS by Gd-EOB-DTPA Enhanced MRI

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04559451
• Other study ID #: PekingUTH-ALPPS
• Status: Recruiting
• Start date: October 1, 2020
• Est. completion date: December 31, 2023

Study information

• Verified date: March 2021
• Source: Peking University Third Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Insufficient future liver remnant (FLR), which may render post-hepatectomy liver failure, is one of the major obstacles for performing liver resection for patients with liver malignants. Associating liver partition and portal vein ligation (ALPPS) was introduced to induce rapid and extensive liver hypertrophy, which offers the opportunity for removing the liver malignancy in the second stage operation for patients with insufficient FLR at their first stage operation. Feasibility of the second stage of ALPPS has been assessed mostly on the basis of laboratory parameters and volumetry by the 3D reconstruction of CT. Meanwhile, part of the patients who underwent the second stage ALPPS still experienced postoperative liver failure, even in patients with sufficient FLR volume. In other words, this volumetric increase may not reflect the increase of liver function. And the laboratory parameters can only partly reflect the global liver function but not the regional liver function. Therefore, the combination of volumetric and global liver function tests might be unsuitable for predicting FLR function after first stage ALPPS because function is distributed unequally between left and right liver lobe. The Gd-EOB-DTPA-enhanced liver MRI, which has remarkable potential to evaluate regional liver function and could therefore be an ideal diagnostic test for performing volumetric and functional measurement after the first stage ALPPS in one examination. Thus we performed this clinical trial in order to evaluate the efficacy of Gd-EOB-DTPA-enhanced liver MRI in evaluating the FLR liver function after the first stage ALPPS.

Description:

The clinical data and follow up information of the patients who underwent laparoscopic ALPPS in Department of General Surgery, Peking University Third Hospital were collected. The indication for the performance of the first and second ALPPS was evaluated by multi-disciplinary team (MDT). The liver function evaluation indexes of Gd-EOB-DTPA Enhanced liver MRI such as RE (Relative enhancement of the liver)=（SI20min-SIunenhanced）/ SIunenhanced and other related indexes were calculated. SI referred to signal intensity. SI20 min referred to the signal intensity in the hepatocyte phase (20 min after the injection). The relationship between the indexes and postoperative liver failure as well as other complications were analyzed.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 31, 2023
• Est. primary completion date: December 31, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• future liver remnant volume <30%;
• indocyanine green clearance (ICG) rate <20% at 15 minutes;
• Child A liver function, serum platelet count > 50×109/L;
• good general condition.

Exclusion Criteria:

• complete right portal vein thrombosis;
• serum platelet count < 50×109/L;
• clinical signs of portal hypertension such as ascites, and/or intra-abdominal varices.

Related Conditions & MeSH terms

• Liver Failure
• Liver Function Failure
• Liver Malignant Tumors
• Liver Neoplasms
• Neoplasms

Locations

Country	Name	City	State
China	Peking University Third Hospital	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Peking University Third Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Postoperative liver function failure	The "50-50 criteria" was applied to assess post-treatment liver failure, which considers the increased total bilirubin level (>50 umol/L) and decreased PTA (<50%) on postoperative day 5.	Within 90 days after the operation
Secondary	Postoperative morbidities and mortalities	Postoperative morbidities and mortalities were graded according to the Clavien classification.	Within 90 days after the operation