Serum GLYcomics to Predict Graft Loss and Mortality After Liver Transplantation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Ghent

About this trial

The first 12 months after liver transplantation (LT) are decisive in posttransplant outcome, as almost half of deaths and two thirds of graft loss requiring retransplant occur in the first year after LT. Since delaying retransplantation in those patients that experience an unfavorable posttransplant course directly impacts their outcome, timely decision making is of paramount importance in these individuals. However, balancing the need and right timing for retransplantation in individual patients with a complicated posttransplant course is currently a difficult challenge that relies on imperfect clinical variables and biomarkers, as well as the experienced judgment of the transplant team.

Building on the findings of a pilot study in liver transplant recipients (n = 131) led by the Ghent University Hospital, we want to validate the prognostic performance of the GlycoTransplantTest on a multicentric scale. In this pilot study, a single glycomic signature at day 7 after LT allowed accurate prediction of graft loss at 3 months after LT. The serum glycome of those patients experiencing graft loss was characterized by increased undergalactosylation and an increased presence of fucosylated and triantennary glycans. After statistical modeling, use of an optimized cutoff based on the relative abundance of 13 serum glycans showed a strong association with graft loss at 3 months (odds ratio 70.211; P\<0.001; 95% CI: 10.876-453.23).

Using sequential measurements of serum glycomics in liver transplant recipients, we want to prospectively study and validate the predictive value of the serum glycomic signature for graft survival and overall survival at 3-months (primary end point) and 12-months after liver transplantation (secondary end point).

Determination of the serum glycomic profile is a high-throughput technique that allows to study and quantify the relative abundance of sugar chains (glycans) anchored at specific sites of serum proteins. This technique has shown a very strong prognostic value for graft loss at 3-months after liver transplantation in a pilot study at the Ghent University Hospital.

In this large-scale multicentric prognostic study, we will collect serum samples of liver transplant recipients at fixed time points.

Apart from the serum glycomic profile, we will collect data from the patients electronic record: demographic data (gender, age), data directly relevant to the indication of transplant (eg. imaging for primary liver cancer, lab values for diagnosis of end-stage liver disease), and outcome data (graft survival, overall survival, follow-up time). This list is non-exhaustive.

Using this approach, we will demonstrate the predictive validity of serum glycomics in liver transplant recipients for graft survival and overall survival at 3- and 12-months post-LT. Building on these data, the use of a simple blood test could differentiate patients at risk of graft loss and thus represent a paradigm shift directing these patients to timely treatment adaptations.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Signed and dated patient informed consent document

Age ≥ 18 years

Ability to comply with protocol-specified evaluations and scheduled visits

Diagnosis of end-stage liver disease, primary hepatic malignancy meeting the Milan criteria for liver transplantation, or acute hepatic failure

Disqualifiers

None

Trial population

Adult patients active on the waiting list or undergoing a liver transplantation. All indications for liver transplantations are eligible.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • GlycoTransplantTest

    Diagnostic test

    Determination of serum glycomics in the early posttransplant stage, using an optimal cutoff based on statistic modeling.

Treatment groups

600 Participants
are divided into 2 treatment groups
Group A: No graft loss1 intervention
Group B: Graft loss1 intervention

Trial outcomes

Primary outcomes

1

Graft loss

Death or need for retransplantation

Time frame
3 months after liver transplantation
2

Mortality

All-cause mortality

Time frame
3 months after liver transplantation

Secondary outcomes

1

Graft loss

Death or need for retransplantation

Time frame
12 months after liver transplantation
2

Mortality

All-cause mortality

Time frame
12 months after liver transplantation

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University Hospital, Ghent

Lead sponsor

Fund for Scientific Research, Flanders, Belgium

Collaborator

University Hospital, Antwerp

Collaborator

Universitaire Ziekenhuizen KU Leuven

Collaborator

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Collaborator