GLITCA: Serum Glycomics as Prognostic and Diagnostic Biomarkers of Disease Recurrence in Liver Transplant Recipients With Hepatocellular Carcinoma

Sponsor
University Hospital, Ghent (Other)
Overall Status
Recruiting
CT.gov ID
NCT05866783
Collaborator
University Hospital, Antwerp (Other), Universitaire Ziekenhuizen KU Leuven (Other), Cliniques universitaires Saint-Luc- Université Catholique de Louvain (Other)
500
1
176.2
2.8

Study Details

Study Description

Brief Summary

Liver transplantation (LT) is the only curative option for a selection of patients with hepatocellular carcinoma (HCC) based on clinical selection criteria known as the Milan criteria. Nevertheless, 15% of these patients still show tumour recurrence after LT. In a monocentric pilot study, we have demonstrated that specific changes in N-glycan profiles (measured before LT) occur in HCC patients receiving LT1. These specific changes proved to be strongly associated with the risk of HCC recurrence and overall death after LT, independent of the criteria used for stringent patient selection. Pathophysiologically, it is known that abberations in protein glycosylation are involved in the onset en development of HCC. As such, a prognostic biomarker was developed that can clearly differentiate between patients with and without increased risk of HCC recurrence.

The primary goal of this research study is to set up a prospective, multicentre study in order to validate the prognostic value of this glycomics-based serum biomarker. As such, the risk of tumour recurrence in patients undergoing LT for HCC will be estimated independent from the Milan criteria and the French alpha-fetoprotein model as the current standard. The secondary goal is to explore the potential of serum glycomics as markers of early recurrence after LT for HCC. More specifically, we aim to investigate whether serial glycomics determination at fixed time points after LT could allow early detection of recurrent HCC even before it is visible on conventional imaging. Consequently, a diagnostic biomarker for monitoring early recurrence after LT could be developed with the potential of redirecting treatment strategies already in an early disease stage.

In case the promising data from the pilot study will be confirmed, the prognostic biomarker could be implemented in daily clinical practice leading to optimization of patient selection using a simple blood test before LT. More specifically, this marker could improve organ allocation thus preventing unnessecary treatment toxicity for the patient and reducing the costs of treatment for society. Moreover, it should be emphasized that a patent application was already submitted and accepted in collaboration with TechTranfer of Ghent University (PCT/EP2021/057788-Prognostic markers of disease recurrence in liver transplant recipients with hepatocellular carcinoma).

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: HCCRecurrencePrognosticScore
  • Diagnostic Test: HCCRecurrenceDiagnosticScore

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
500 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Serum Glycomics as Prognostic and Diagnostic Biomarkers of Disease Recurrence in Liver Transplant Recipients With Hepatocellular Carcinoma
Actual Study Start Date :
Apr 28, 2023
Anticipated Primary Completion Date :
Jan 1, 2027
Anticipated Study Completion Date :
Jan 1, 2038

Arms and Interventions

Arm Intervention/Treatment
No HCC recurrence

Patients receiving a liver transplantation that do NOT develop HCC recurrence after liver transplantation.

Diagnostic Test: HCCRecurrencePrognosticScore
Determination of serum glycomics pre-transplant using an optimal cutoff based on statistic modeling

Diagnostic Test: HCCRecurrenceDiagnosticScore
Determination of serum glycomics post-transplant using an optimal cutoff based on statistic modeling

HCC recurrence

Patients receiving a liver transplantation that develop HCC recurrence after liver transplantation.

Diagnostic Test: HCCRecurrencePrognosticScore
Determination of serum glycomics pre-transplant using an optimal cutoff based on statistic modeling

Diagnostic Test: HCCRecurrenceDiagnosticScore
Determination of serum glycomics post-transplant using an optimal cutoff based on statistic modeling

Outcome Measures

Primary Outcome Measures

  1. HCC recurrence [18 months]

  2. Disease-free survival [18 months]

Secondary Outcome Measures

  1. Overall survival [10 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Signed and dated patient informed consent document

  • Diagnosis of hepatocellular carcinoma

  • Age ≥ 18 years

  • Ability to comply with protocol-specified evaluations and scheduled visits

  • Eligible for liver transplantation and/or active on the waiting list for liver transplantation

  • Consulted the department of Gastroenterology and Hepatology

Exclusion Criteria:
  • Diagnosis of other liver tumors (eg. liver metastasis, cholangiocarcinoma)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ghent University Hospital Gent Belgium 9000

Sponsors and Collaborators

  • University Hospital, Ghent
  • University Hospital, Antwerp
  • Universitaire Ziekenhuizen KU Leuven
  • Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT05866783
Other Study ID Numbers:
  • ONZ-2022-0492
First Posted:
May 19, 2023
Last Update Posted:
May 19, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 19, 2023