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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentro di Riferimento Oncologico - Aviano

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Treatment for other oncological diseases

Immunodepression congenital or acquired (HIV, organ transplantation, pharmacological)

Trial population

The study population consists of patients with varying degrees of liver damage, diagnosed with of HCC or HCV-positive with diagnosed cirrhosis, fibrosis or long-term HCV infection

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Difference in antibody profile between subjects with and without chronic HCV infection

Mean or median difference between the groups, as appropriate, will be calculated

Time frame
up to 2 years
2

Difference in antibody profile between subjects with chronic HCV infection receiving or not receiving DAA therapy

Mean or median difference between the groups, as appropriate, will be calculated

Time frame
up to 2 years

Secondary outcomes

1

Define a relationship between IgG levels toward HCV-specific peptides and viral load/development clinical after 2 years of follow-up

Correlation coefficient between the highest IgG levels towards at least one specific HCV peptide and high viral load will be calculated

Time frame
up to 2 years
2

Define a relationship between IgG levels toward HCV-specific peptides and HCV genotype

Relation will be analyzed with logistic regression analysis and represented with Odds Ratio (OR) and relative 95% Confidence Interval (95% CI)

Time frame
up to 2 years
3

Characterization of Interferon Lambda 4 (INFL4) and Human Leukocyte antigene (HLA-E) variants within patient with or without HCV related hepatocarcinoma (HCC)

Frequencies of genetic variants within patient with or without HCV related hepatocarcinoma (HCC) will be reported

Time frame
up to 2 years
4

Characterization of INFL4 and HLA-E variants within patient with or without HCV related chronic hepatitis

Frequencies of genetic variants within patient with or without HCV related chronic hepatitis will be reported

Time frame
up to 2 years

Other outcomes

Sponsors and contacts

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