About this trial
The aim is to determine the metabolic factors, host immune factors, and medical imaging data associated with the development of HepatoCellular Carcinoma (HCC) in patients with alcohol-related liver disease or dysmetabolic steatosis/Non-Alcoholic SteatoHepatitis.
The investigators will include patients with and without cirrhosis in order to identify early molecular mechanisms involved in the development of HCC especially in non-cirrhotic patients.
Eligibility criteria
Qualifiers
Affiliation to French social security.
Male or female ≥ 18 years of age
Patients able to receive and understand information about the research and to give written informed consent duly signed by the patient and the investigator (at the latest on the day of inclusion and before any examination necessary for the research).
Alcohol consumption ≤ 30 g pure alcohol/d (or 210 g pure alcohol/week) for men and ≤ 20 g pure alcohol/d (140 g pure alcohol/week) for women.
Disqualifiers
Positive HIV serology
Patients with detectable hepatitis C viral load
Presence of Hbs antigen
History of autoimmune hepatitis type 1 or 2, primary biliary cholangitis, primary sclerosing cholangitis, Wilson's disease, genetic haemochromatosis homozygous, alpha1 anti-trypsin deficiency
Trial design
Treatments tested in this trial
- Liver biopsy
Treatment groups
Sponsors and collaborators
Institut National de la Santé Et de la Recherche Médicale, France
Lead sponsor
Centre Hospitalier Universitaire de Nice
Collaborator