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

60 Participants
are divided into 1 treatment group

Locations

1
CHU Montpellier Montpellier France

Sponsors and collaborators

University Hospital, Montpellier

Lead sponsor