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NCT Number: NCT05866796

Serum GLYcomics to Predict Graft Loss and Mortality After Liver Transplantation

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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
  • Eligible for liver transplantation and/or active on the waiting list for liver transplantation. Individuals eligible and/or active on the waiting list for multiple organ transplantation including the liver (eg. Combined liver and kidney transplantation, or intestinal transplantation) are also eligible for inclusion.
  • Consulted the department of Gastroenterology and Hepatology at Ghent University Hospital

Exclusion criteria

  • Transplantation of one or more organs not including the liver

Treatment and study plan

GlycoTransplantTest

Diagnostic Test

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

Primary outcomes

  1. Graft loss

    Time frame: 3 months after liver transplantation

    Death or need for retransplantation

  2. Mortality

    Time frame: 3 months after liver transplantation

    All-cause mortality

Secondary outcomes

  1. Graft loss

    Time frame: 12 months after liver transplantation

    Death or need for retransplantation

  2. Mortality

    Time frame: 12 months after liver transplantation

    All-cause mortality

Study contacts

Contact information is provided by the study sponsor or research team.

Lorenz Grossar, MD

CONTACT

[email protected]

0032 494 088 789

Xavier Verhelst, MD, PhD

CONTACT

[email protected]

0032 9 332 23 71

Sponsors and collaborators

Lead sponsor

University Hospital, Ghent

Other

Collaborators

  • Cliniques universitaires Saint-Luc- Université Catholique de Louvain
  • Fund for Scientific Research, Flanders, Belgium
  • Universitaire Ziekenhuizen KU Leuven
  • University Hospital, Antwerp

Registry information

Official study title

Validation of Serum GLYcomics to Predict Graft Loss and Mortality After Liver Transplantation

Acronym: GLYGALT

Important dates

Study start
2023
Primary completion
2026
Study completion
2027
First posted
May 19, 2023
Registry last updated
May 16, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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