Clinical trial · Observational
Cohort Study of Patients With Hepatocellular Carcinoma and Circulating Tumor DNA Monitoring of Chemoembolization
NCT05390112CI-TRIAL-00058706Mona-LisaunknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Cohort study to assess the impact of ctDNA detection in the follow-up and management of patients with hepatocellular carcinoma treated by TACE
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Circulating Tumor DNA | — | UNRESOLVED | — |
| Hepatocellular Carcinoma Non-resectable | — | UNRESOLVED | — |
| Transarterial Chemoembolization | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| DNA | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Radiological response at 1 month according to mRECIST and ctDNA detection
- timeFrame
- 4 to 6 weeks
- description
- radiological response : mRECIST (progressive disease; stable disease, partial response, complete response) LIRADS (LR-TR Nonviable, LR-TR Equivocal, LR-TR Viable); ctDNA at 1 month detection (yes or no)
Secondary outcomes (1)
- measure
- Progression-free survival and overall survival
- timeFrame
- 4 to 6 weeks
- description
- progression-free Survival and overall Survival (months)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Age ≥ 18 years * 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 with non-tumor liver parenchyma) at the portal phase or late phase compared with non-tumor parenchyma. * Histologically diagnosed HCC in the absence of an imaging diagnosis * Patient with a first TACE (naive) or not, regardless of the number of previous procedures * Patient naïve or on a new line of oncological treatment, regardless of the number of previous lines of treatment. * Treatment decision validated by the digestive oncology staff. * Patient having read and understood the information letter and signed the informed consent. * Patient follow-up performed at the Charles Nicolle University Hospital in Rouen. Exclusion Criteria : * Other active cancer or hematological malignancy, currently being treated * Patient not affiliated to the social security system * Pregnant woman or woman in labour or breastfeeding * Person deprived of liberty by an administrative or judicial decision * Person placed under court protection
References
Publications (0)
Data not yet available
No reference posted for this study.