Serum GLYcomics to Predict Graft Loss and Mortality After Liver Transplantation
GLYGALT
Validation of Serum GLYcomics to Predict Graft Loss and Mortality After Liver Transplantation
1 other identifier
observational
600
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2023
Longer than P75 for all trials
1 active site
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 Start
First participant enrolled
April 26, 2023
CompletedFirst Submitted
Initial submission to the registry
May 10, 2023
CompletedFirst Posted
Study publicly available on registry
May 19, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 26, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2027
ExpectedMay 16, 2024
May 1, 2024
3 years
May 10, 2023
May 14, 2024
Conditions
Keywords
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.
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.
Interventions
Determination of serum glycomics in the early posttransplant stage, using an optimal cutoff based on statistic modeling.
Eligibility Criteria
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
- University Hospital, Ghentlead
- Fund for Scientific Research, Flanders, Belgiumcollaborator
- University Hospital, Antwerpcollaborator
- Universitaire Ziekenhuizen KU Leuvencollaborator
- Cliniques universitaires Saint-Luc- Université Catholique de Louvaincollaborator
Study Sites (1)
Xavier Verhelst
Ghent, Flanders, 9000, Belgium
Biospecimen
Serum samples for glycomics analysis
Central Study Contacts
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