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Evaluation of the Circulating Epigenetic Biomarker mSEPT9 for Predicting the Occurrence of Hepatocellular Carcinoma in Patients With Cirrhosis: A Prospective Multicenter Trial (SEPT9_SuRV)

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

This study aims to evaluate the role of the circulating epigenetic biomarker mSEPT9 in predicting the risk of hepatocellular carcinoma (HCC) in patients with cirrhosis. HCC is a primary liver cancer that frequently develops in individuals with cirrhosis, and early detection is critical for improving outcomes. This research involves 400 patients with cirrhosis who will be followed every six months for up to 60 months. During these visits, blood samples will be collected to analyze mSEPT9 levels. By identifying changes in this biomarker, the study seeks to improve early diagnosis and personalize surveillance strategies, potentially enhancing patient survival and quality of life.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
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• Adults aged 18 years or older.

• Patients diagnosed with cirrhosis confirmed by clinical, biochemical, radiological, or histological criteria.

• Cirrhosis attributable to one or more of the following etiologies: alcohol, hepatitis C (HCV), hepatitis B (HBV), nonalcoholic steatohepatitis (NASH), hemochromatosis, autoimmune hepatitis, primary biliary cholangitis, primary sclerosing cholangitis, or cryptogenic causes.

• Patients actively followed in one of the participating study centers.

• Patients affiliated with a social security program or equivalent.

• Patients with a body weight greater than 45 kg.

• Patients who have been fully informed about the study procedures and have provided oral informed consent.

Locations
Other Locations
France
Regional and University Hospital Center of Nancy
RECRUITING
Vandœuvre-lès-nancy
Contact Information
Primary
Prof. Abderrahim OUSSALAH, MD, PhD
abderrahim.oussalah@univ-lorraine.fr
+33383153629
Time Frame
Start Date: 2025-06-03
Estimated Completion Date: 2033-06-03
Participants
Target number of participants: 400
Treatments
Patients With Cirrhosis Without Hepatocellular Carcinoma at Baseline
This cohort includes 400 patients with cirrhosis who do not have hepatocellular carcinoma (HCC) at the time of inclusion. Participants will undergo standard clinical, biological, and radiological evaluations every six months for a total follow-up duration of 60 months, in accordance with international guidelines for cirrhosis management. In addition to routine assessments, blood samples will be collected at each visit for the analysis of the circulating epigenetic biomarker mSEPT9. This biomarker will be tested to evaluate its utility in predicting the occurrence of HCC during the follow-up period. The results of the mSEPT9 test will not influence clinical management during the study.
Related Therapeutic Areas
Sponsors
Collaborators: New Day Diagnostics
Leads: Central Hospital, Nancy, France

This content was sourced from clinicaltrials.gov