About this trial
The goal of this prospective clinical trial is to identify a predictive biomarker in patients with advanced HCC (stage B and C) using a combinatorial approach of the liquid biopsy.
The main questions it aims to answer are:
* Is multi-omic liquid biopsy approach able to identify a strong predictive biomarker of immunotherapy efficiency? * Is there a correlation between tissue biopsy (PD-L1 tissue level of expression) and liquid biopsy (detection of CTC expressing PD-L1) in HCC patients?
Participants blood will be collected at several time points.
Eligibility criteria
Qualifiers
Patients of at least 18 years old,
Patients with advanced hepatocellular carcinoma or HCC with indication for first-line PD-1 or PD-L1 immunotherapy in MDT, without prior systemic therapy,
The diagnosis of HCC is established according to imaging criteria (LI-RADSv2018 criteria) or after histological evidence,
Advanced HCC defined by BCLC stages B and C,
Disqualifiers
Administration of a previous systemic anti-tumor treatment (immunotherapy or chemotherapy or targeted therapy)
No personal history of neoplasia in the previous 5 years
No personal history of systemic inflammatory diseases
No immunosuppressive treatment or treatment that could modify immunity (anti-TNF...)
Trial design
Treatments tested in this trial
- Liquid Biopsy
Treatment groups
Locations
1Sponsors and collaborators
University Hospital, Montpellier
Lead sponsor