Liver Cancer and Immunotherapy in the Liquid Biopsy Era (LILIPSY)
Hepatocellular Carcinoma, BCLC Stage B Hepatocellular Carcinoma, BCLC Stage C Hepatocellular Carcinoma
About this trial
This is an interventional other trial for Hepatocellular Carcinoma focused on measuring Hepatocellular Carcinoma, BCLC Stage B and C, Immune Checkpoint Inhibitor, Liquid Biopsy, Precision Medicine
Eligibility Criteria
Inclusion Criteria: 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, Patients with oral consent. Exclusion Criteria: 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...) No affiliation or non-beneficiary of a Social Security system; Vulnerable persons according to article L1121-6 of the CSP ; Persons of full age who are protected or unable to give their consent according to article L1121-8 of the CSP; Pregnant or breastfeeding women according to article L1121-5 of the CSP. Non-inclusion due to follow-up difficulties (transfer, insufficient motivation, poor compliance, priority associated pathology in care, etc.)
Sites / Locations
Arms of the Study
Arm 1
Experimental
BCLC B and C HCC patients
For each participant, 30mL of blood will be collected at inclusion/before treatment initiation (baseline) and during standard of care follow-up. The blood sample will be taken, in consultation or in outpatient clinic during a blood test for health purposes.