NCT05866796

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
600

participants targeted

Target at P75+ for all trials

Timeline
12mo left

Started Apr 2023

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress76%
Apr 2023May 2027

Study Start

First participant enrolled

April 26, 2023

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

May 10, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 19, 2023

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 26, 2026

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2027

Expected
Last Updated

May 16, 2024

Status Verified

May 1, 2024

Enrollment Period

3 years

First QC Date

May 10, 2023

Last Update Submit

May 14, 2024

Conditions

Keywords

GlycomicsLiver transplantationGraft survival

Outcome Measures

Primary Outcomes (2)

  • Graft loss

    Death or need for retransplantation

    3 months after liver transplantation

  • Mortality

    All-cause mortality

    3 months after liver transplantation

Secondary Outcomes (2)

  • Graft loss

    12 months after liver transplantation

  • Mortality

    12 months after liver transplantation

Study Arms (2)

No graft loss

Patients receiving liver transplantation that do NOT experience graft loss within 3-months or 12-months after liver transplantation.

Diagnostic Test: GlycoTransplantTest

Graft loss

Patients receiving liver transplantation that experience graft loss within 3-months or 12-months after liver transplantation. Graft loss is defined as either death of the liver transplant recipient (all-cause), or need for retransplantation of the liver.

Diagnostic Test: GlycoTransplantTest

Interventions

GlycoTransplantTestDIAGNOSTIC_TEST

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

Graft lossNo graft loss

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

  • 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
  • Consulted the department of Gastroenterology and Hepatology at Ghent University Hospital

You may not qualify if:

  • \- Transplantation of one or more organs not including the liver

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Xavier Verhelst

Ghent, Flanders, 9000, Belgium

RECRUITING

Biospecimen

Retention: SAMPLES WITHOUT DNA

Serum samples for glycomics analysis

Central Study Contacts

Xavier Verhelst, MD, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 10, 2023

First Posted

May 19, 2023

Study Start

April 26, 2023

Primary Completion

April 26, 2026

Study Completion (Estimated)

May 1, 2027

Last Updated

May 16, 2024

Record last verified: 2024-05

Locations