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NCT06718530Recruiting

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

Source: ClinicalTrials.gov · Last updated 5 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1000 (estimated)
First submitted
2 Dec 2024
Start date
13 May 2024
Primary completion date
31 Dec 2026
Lead sponsor
Centro di Riferimento Oncologico - Aviano
NCT number
NCT06718530

What you commit to

  • Study type: Observational
  • Planned participants: 1000
  • From 13 May 2024 to the primary completion date, 31 Dec 2026
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Treatment for other oncological diseases
  • Immunodepression congenital or acquired (HIV, organ transplantation, pharmacological)

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centro di Riferimento Oncologico (CRO) di Aviano - IRCCS
Coordinator of this site? Confirm its status
AvianoItalyRecruiting
AORN S.Anna e S. Sebastiano, Via F. Palasciano
Coordinator of this site? Confirm its status
CasertaItalyRecruiting
Istituto Nazionale Tumori di Napoli, IRCCS "G. Pascale"
Coordinator of this site? Confirm its status
NaplesItalyRecruiting
Dip. Univ. Clin. di Scienze mediche, chirurgiche e della salute Università di Trieste
Coordinator of this site? Confirm its status
TriesteItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.