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Recruiting Not applicable

Prediction of Hepatocellular Carcinoma Recurrence After Curative Treatment by Monitoring Circulating Tumor DNA

NCT05375370 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2022-08-04
Last updated
2026-02-06

Condition(s) studied

Hepatocellular Carcinoma

Investigational drug(s) / intervention(s)

circulating tumor DNA dosage

circulating tumor DNA dosage: blood sample for circulating tumor DNA dosage will be done to patient with hepatocellular carcinoma

Study summary

The goal of the REMNANT study is to confirm the clinical value of detecting a new biomarker, ctDNA (circulating tumor DNA), in the follow-up of patients with operated liver cancer. In order to meet this objective, this biomarker will be measured in your blood before and after surgery, at three and six months.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥ 18 years 2. HCC diagnosed on consensus radiological criteria in cirrhotic patients (EASL-EORTC 2012): helical CT or MRI with triple arterial, portal and late acquisition. The diagnosis is based on the presence of hypervascularization at the early arterial time (wash-in) with wash-out (hypodensity or hypointensity compared to non-tumor liver parenchyma) at the portal phase or late phase compared to non-tumor parenchyma. 3. HCC diagnosed histologically in the absence of a diagnosis on imaging (see IC n°2 above) 4. Patient operated on for liver resection or radiofrequency destruction 5. Treatment decision validated by the digestive oncology PCR 6. Patient having read and understood the information letter and signed the non-opposition form 7. Patient follow-up at the Charles Nicolle University Hospital in Rouen Exclusion Criteria: 1. Other active cancer or hematological malignancy 2. Contra-indication to surgery 3. Patient not affiliated to the social security system 4. Pregnant woman or parturient or breastfeeding 5. Person under court protection, sub guardianship or curatorship

Primary outcome measure(s)

  • Change in tcNA dosage between baseline and 6 Months — 6 months
    evolution of tcDNA percentage between Baseline and at 6 months after surgery
  • Change in tcDNA dosage between baseline and 3 Months — 3 months
    evolution of tcDNA percentage between Baseline and at 3 months after surgery

Trial sites (1)

FacilityCityRegionStatus
Chu Rouen Rouen France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05375370 on ClinicalTrials.gov ↗ ← All trials in France