Ireland
--:--IST
Recruiting Observational

Characterization of Immune Genotypes and Antibody Profiles to Foster the discoVERY of diagnosticbioMARKERS of Liver Cancer Development

NCT06718530 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2024-05-13
Last updated
2024-12-05

Condition(s) studied

Hepatitis C Virus Infection

Study summary

Hepatitis C virus (HCV), which infects more than 185 million people, is a major risk factor. Direct-acting antiviral (DAA) therapy has significantly improved the eradication of the virus, but has not completely eliminated the risk of HCC, so careful surveillance is necessary. The genetic diversity of the natural killer receptor, histocompatibility antigens (HLA) and interferon lambda 4 (INFL4) activity, among other factors, have been found to be crucial in directing disease progression. Importantly, these markers are detectable years before the diagnosis of HCC. In addition, polymorphic variants attributable to the expression of genes involved in innate-type immune response, such as IFNL4 and HLA-E, have been shown to be predictive for the development of HCC and have not yet been extensively studied. The aim of the study is to evaluate novel circulating biomarkers, including the presence of antibodies to specific HCV proteome peptides, IFNL4 expression, and the interaction of specific HLA receptors/ligands in a large cohort of HCV-positive subjects in order to create a screening strategy for the early diagnosis of HCV-associated HCC.

Part of the study will be devoted to describing the immune microenvironment associated with the expression of IFNL4 and HLAE, evaluating them as potential prognostic indicators for HCC in HCV-infected subjects undergoing surgery for HCC, as well as in those with advanced/metastatic HCC.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients aged ≥18 years with the presence of chronic infection, fibrosis, cirrhosis or HCV- associated HCC * Patients able to understand and willing to sign the of informed consent * Patients to answer the questions in the questionnaire of enrollment Exclusion Criteria: * Treatment for other oncological diseases * Immunodepression congenital or acquired (HIV, organ transplantation, pharmacological)

Primary outcome measure(s)

  • Difference in antibody profile between subjects with and without chronic HCV infection — up to 2 years
    Mean or median difference between the groups, as appropriate, will be calculated
  • Difference in antibody profile between subjects with chronic HCV infection receiving or not receiving DAA therapy — up to 2 years
    Mean or median difference between the groups, as appropriate, will be calculated

Trial sites (4)

FacilityCityRegionStatus
Centro di Riferimento Oncologico (CRO) di aviano-IRCCS Aviano Pordenone Recruiting
AORN S.Anna e S. Sebastiano, Via F. Palasciano Caserta Italy Recruiting
Istituto Nazionale Tumori di Napoli, IRCCS "G. Pascale" Naples Italy Recruiting
Dip. Univ. Clin. di Scienze mediche, chirurgiche e della salute Università di Trieste Trieste Italy Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06718530 on ClinicalTrials.gov ↗ ← All trials in Italy