Liver Diseases: Extracellular Vesicles as Biomarkers

NCT ID: NCT07185360

Last Updated: 2025-09-22

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 845 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-09-22
• Study Completion Date: 2028-03-31

Brief Summary

Worldwide, cirrhosis is responsible for 2 million deaths per year. Hepatocellular carcinoma (HCC) accounts for 800,000 of these deaths and is the 3rd leading cause of cancer related death. Cirrhosis affects mainly a working age population, hence its heavy economic burden.While patients with compensated cirrhosis do not have symptoms and have a 10-year life expectancy, decompensation of cirrhosis heralds a dramatic decrease in life expectancy to 2 years. Biomarkers allowing reliable estimation of the risk for decompensation of cirrhosis would allow community-based care, possibly by nurse practitioners, of patients at low risk, while patients had high risk could be managed in secondary and tertiary care centers and included in clinical trials. Because HCC is usually asymptomatic at early stages, when it is still curable, it can easily be missed. Biomarkers allowing stratification of the risk of HCC would allow reinforced surveillance (using magnetic resonance imaging) of high-risk patients, and their inclusion in chemoprevention clinical trials.

LIVER-TRACK aims at reliably predicting the outcome of patients with compensated cirrhosis through the development of a Tests for Decompensation and a Test for HCC. This will be achieved through leveraging circulating extracellular vesicles (EVs), an untapped source of biomarkers in liver diseases, as prognostic indicators, and combining them with existing blood biomarkers and single-nucleotide polymorphisms (SNPs). LIVER-TRACK also aims at delivering technologies for EV measurement that are useable in medical practice.

Detailed Description

Worldwide, cirrhosis is responsible for 2 million deaths per year. Hepatocellular carcinoma (HCC) accounts for 800,000 of these deaths and is the 3rd leading cause of cancer related death. Cirrhosis affects mainly a working age population, hence its heavy economic burden. While patients with compensated cirrhosis do not have symptoms and have a 10-year life expectancy, decompensation of cirrhosis heralds a dramatic decrease in life expectancy to 2 years. Biomarkers allowing reliable estimation of the risk for decompensation of cirrhosis would allow community-based care, possibly by nurse practitioners, of patients at low risk, while patients had high risk could be managed in secondary and tertiary care centers and included in clinical trials. Because HCC is usually asymptomatic at early stages, when it is still curable, it can easily be missed. Biomarkers allowing stratification of the risk of HCC would allow reinforced surveillance (using magnetic resonance imaging) of high-risk patients, and their inclusion in chemoprevention clinical trials.

LIVER-TRACK aims at reliably predicting the outcome of patients with compensated cirrhosis through the development of a Tests for Decompensation and a Test for HCC. This will be achieved through leveraging circulating extracellular vesicles (EVs), an untapped source of biomarkers in liver diseases, as prognostic indicators, and combining them with existing blood biomarkers and single-nucleotide polymorphisms (SNPs). LIVER-TRACK also aims at delivering technologies for EV measurement that are useable in medical practice.

LIVER-TRACK outputs are expected to: i) improve care for individual patients at highest medical need, i.e., patients with cirrhosis with high risk of decompensation or HCC; ii) decrease cirrhosis burden for public health, iii) facilitate drug development; and iv) technically allow exploitation of EVs as biomarkers in clinical practice, an obligatory step permitting expansion to other fields such as cancer and cardiovascular diseases.

Conditions

Liver Diseases

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Volunteers without liver disease

Volunteers without liver disease

Group Type: OTHER

blood sampling for volunteers

Intervention Type: OTHER

A 38.5 ml blood sample will be taken to test for research taken to test for research

Diabetic patients with F3/F4 fibrosis recruited and followed prospectively

Diabetic patients with F3/F4 fibrosis recruited and followed prospectively

Group Type: OTHER

blood sampling for diabetics patients with F3/F4 fibrosis

Intervention Type: OTHER

32.5 ml will be sampled at inclusion, at one year visit and two year visit

Patients with liver disease

Patients with liver disease

Group Type: OTHER

blood sampling for patients with liver disease

Intervention Type: OTHER

A blood sample of 35.5 mL maximum will be taken for research purposes at the inclusion visit, M1 visit and M3 visit.

Interventions

blood sampling for volunteers

A 38.5 ml blood sample will be taken to test for research taken to test for research

Intervention Type: OTHER

blood sampling for diabetics patients with F3/F4 fibrosis

32.5 ml will be sampled at inclusion, at one year visit and two year visit

Intervention Type: OTHER

blood sampling for patients with liver disease

A blood sample of 35.5 mL maximum will be taken for research purposes at the inclusion visit, M1 visit and M3 visit.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Patient aged 18 or over
• Type 2 diabetic (ADA/WHO criteria recalled in section 20.5)
• Hepatic fibrosis stage F3/F4 on liver biopsy or hepatic elasticity > 10 kPa

• Major
• Child-Pugh A, B or C cirrhosis, diagnosed on the basis of histological evidence or liver elasticity > 15 kPa or a combination of biological and radiological signs.

Exclusion Criteria

• Known liver disease
• Active cancer
• Viral or bacterial infection within 2 weeks of inclusion (respiratory, dermatological, urinary, digestive, etc.)
• Transfusion in the month preceding inclusion
• Current participation or less than 3 months' participation in a therapeutic interventional trial
• Absence of signed informed consent
• Not affiliated to a social security scheme
• Pregnant women
• Person under guardianship or trusteeship

Diabetic patients with F3/F4 fibrosis recruited and followed prospectively

Vulnerable person: a person deprived of liberty by a judicial or administrative decision, or under psychiatric care, and a person admitted to a health or social institution for purposes other than research.

• Protected adult
• Not affiliated to or not benefiting from a social security scheme
• Pregnant or breast-feeding women
• Absence of signed informed consent
• Illness linked to other etiologies:

• Alcoholic liver disease
• Current hepatitis B virus infection
• Current hepatitis C virus infection
• Autoimmune hepatitis according to according to AASLD and EASL recommended criteria
• Transferrin saturation >50%
• Alpha antitrypsin ZZ or SZ type deficiency
• Wilson's disease
• Liver transplant patients
• Ultrasound obstruction of blood vessels or bile ducts (on routine ultrasound). If nothing is mentioned on the report, it is considered that there is no obstruction of the blood vessels or bile ducts).
• Current participation or less than 3 months' participation in a therapeutic interventional trial

Patients with liver disease :

• Presence of one of the following diseases in the 15 days prior to inclusion: acute renal failure, bacterial infection (proven or suspected on clinico-biological criteria), digestive bleeding,
• alcoholic hepatitis in the month prior to inclusion
• Previous porto-systemic shunt, liver transplantation, primary sclerosing cholangitis, primary biliary cholangitis, Budd-Chiari syndrome
• Active or past hepatocellular carcinoma
• Active extrahepatic neoplasia,
• Current participation or less than 3 months' participation in a therapeutic interventional trial
• Absence of signed informed consent
• Non affiliation to a social security scheme
• Pregnant or breast-feeding
• Person under guardianship or trusteeship

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Pierre Emmanuel RAUTOU

Role: PRINCIPAL_INVESTIGATOR

APHP

Locations

Bichat Hospital, Beaujon Hospital, Cochin Hospital and Lariboisière Hospital

Paris, France, France

Countries

France

Central Contacts

Pierre Emmanuel RAUTOU

Role: CONTACT

pierre-emmanuel.rautou@aphp.fr

+33 1 40 87 52 83

Facility Contacts

Pierre Emmanuel RAUTOU

Role: primary

pierre-emmanuel.rautou@aphp.fr

+33 1 40 87 52 83

Other Identifiers

APHP250409

Identifier Type: -

Identifier Source: org_study_id