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Liver Cancer and Immunotherapy in the Liquid Biopsy Era (LILIPSY)

Primary Purpose

Hepatocellular Carcinoma, BCLC Stage B Hepatocellular Carcinoma, BCLC Stage C Hepatocellular Carcinoma

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Liquid Biopsy
Sponsored by
University Hospital, Montpellier
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

    Arm Type

    Experimental

    Arm Label

    BCLC B and C HCC patients

    Arm Description

    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.

    Outcomes

    Primary Outcome Measures

    Percentage of patients with CTCs-PD-L1+ by CellSearch® technique
    A CTC is being defined as: EpCAM(+)/PanCK(+)/Dapi(+)/CD45(-). The PD-L1 status will be observed only on these cells. CTC-PD-L1- = 0 vs CTC-PD-L1+ ≥1

    Secondary Outcome Measures

    Number of CTCs-PD-L1+ measured by CellSearch® technique
    0 vs. 1 vs. 2-3 vs. 4 vs. ≥5
    Presence of CTCs at inclusion by CellSearch® technique
    Percentage of patients with CTCs
    Number of CTCs measured by CellSearch® technique
    0 vs 1 vs 2-3 vs 4 vs ≥5
    Immune profiling
    FACS study of immune system cells (T cells, NK cells, B cells, macrophages, immune-checkpoint and platelets)
    Expression of PD-L1 by immuno-histochemical analysis of tissue samples
    PD-L1 expression on biopsy or surgical specimen previously preserved in the Montpellier University Hospital tumor library
    Tumor control defined by mRECIST criteria
    Best response: complete response + partial response + stable vs progression
    Tumor control defined by RECIST criteria
    Best response: complete response + partial response + stable vs progression
    Overall Survival
    Time from immunotherapy start date to date of death from any cause
    Progression Free Survival
    Time from immunotherapy start date to date of first progression or date of death from any cause

    Full Information

    First Posted
    March 30, 2023
    Last Updated
    April 18, 2023
    Sponsor
    University Hospital, Montpellier
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05810402
    Brief Title
    Liver Cancer and Immunotherapy in the Liquid Biopsy Era
    Acronym
    LILIPSY
    Official Title
    Liver Cancer and Immunotherapy : Clinical Relevance of LIquid BioPSY
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    May 2023 (Anticipated)
    Primary Completion Date
    December 2026 (Anticipated)
    Study Completion Date
    May 2027 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University Hospital, Montpellier

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    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.
    Detailed Description
    In solid cancers, some more aggressive tumor cells actively detach from the primary lesion and then travel through the circulating compartment to reach distant organs and form micro-metastases. Detecting CTCs in the blood is also relevant for assessing tumor progression, prognosis and therapeutic follow-up. The non-invasive, highly sensitive for CTCs analysis is called "liquid biopsy". Over the past few years, a multi-analyses approach (CTCs, circulating tumor DNA, extracellular vesicles, miRNA...) of liquid biopsy has been developed. Hepatocellular carcinoma (HCC) is the predominant pathological type of primary liver cancer. It represents the sixth most common incidence worldwide and the third most common cause of cancer mortality. Since 2021, the gold standard treatment for patients with advanced and/or unresectable HCC is the combination of atezolizumab (anti-PD-L1) and bevacizumab (VEGF inhibitor) in cases where chemoembolization is not indicated (patients with lymph node invasion and/or distant lesions or patients with portal flow abnormality). Indeed, this therapy offers a significant benefit in overall survival (19.2 vs 13.4 months, HR 0.66, p<0.0009) as well as in progression-free survival (6.9 vs 4.3 months, HR 0.65, p=0.0001). However, to date, there is no predictive biomarker for the efficacy of immune checkpoint inhibitors (ICI) The purpose of this research project is to identify a predictive biomarker in patients with advanced HCC (stage B and C) using a combinatorial approach of the liquid biopsy (CTC, CTC expressing PD-L1, immune cell profiling).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Hepatocellular Carcinoma, BCLC Stage B Hepatocellular Carcinoma, BCLC Stage C Hepatocellular Carcinoma, Immune Checkpoint Inhibitor, Liquid Biopsy
    Keywords
    Hepatocellular Carcinoma, BCLC Stage B and C, Immune Checkpoint Inhibitor, Liquid Biopsy, Precision Medicine

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Model Description
    Homogenous cohort of BCLC Stage B and C hepatocellular carcinoma patients that will undergo immunotherapy +/- anti-angiogenic agent (bevacizumab)
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    BCLC B and C HCC patients
    Arm Type
    Experimental
    Arm Description
    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.
    Intervention Type
    Biological
    Intervention Name(s)
    Liquid Biopsy
    Other Intervention Name(s)
    Blood sample
    Intervention Description
    30mL blood sample: 1 x 10mL CellSave tube specifically designed for the collection and preservation of CTCs for CellSearch® analysis 1 EDTA tube for PBMCs isolation and circulating immune cells study (5mL), 2 EDTA tubes and 1 dry tube (15mL) for the preparation of the biobank (serum, plasma and cell).
    Primary Outcome Measure Information:
    Title
    Percentage of patients with CTCs-PD-L1+ by CellSearch® technique
    Description
    A CTC is being defined as: EpCAM(+)/PanCK(+)/Dapi(+)/CD45(-). The PD-L1 status will be observed only on these cells. CTC-PD-L1- = 0 vs CTC-PD-L1+ ≥1
    Time Frame
    At inclusion
    Secondary Outcome Measure Information:
    Title
    Number of CTCs-PD-L1+ measured by CellSearch® technique
    Description
    0 vs. 1 vs. 2-3 vs. 4 vs. ≥5
    Time Frame
    At inclusion
    Title
    Presence of CTCs at inclusion by CellSearch® technique
    Description
    Percentage of patients with CTCs
    Time Frame
    At inclusion
    Title
    Number of CTCs measured by CellSearch® technique
    Description
    0 vs 1 vs 2-3 vs 4 vs ≥5
    Time Frame
    At inclusion
    Title
    Immune profiling
    Description
    FACS study of immune system cells (T cells, NK cells, B cells, macrophages, immune-checkpoint and platelets)
    Time Frame
    24 month follow up
    Title
    Expression of PD-L1 by immuno-histochemical analysis of tissue samples
    Description
    PD-L1 expression on biopsy or surgical specimen previously preserved in the Montpellier University Hospital tumor library
    Time Frame
    At inclusion
    Title
    Tumor control defined by mRECIST criteria
    Description
    Best response: complete response + partial response + stable vs progression
    Time Frame
    24 month follow up
    Title
    Tumor control defined by RECIST criteria
    Description
    Best response: complete response + partial response + stable vs progression
    Time Frame
    24 month follow up
    Title
    Overall Survival
    Description
    Time from immunotherapy start date to date of death from any cause
    Time Frame
    24 month follow-up
    Title
    Progression Free Survival
    Description
    Time from immunotherapy start date to date of first progression or date of death from any cause
    Time Frame
    24 month follow-up

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    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.)
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Thomas Bardol, M.D.
    Phone
    +33682882757
    Email
    t-bardol@chu-montpellier.fr
    First Name & Middle Initial & Last Name or Official Title & Degree
    Catherine Guillemare
    Phone
    +33467332304
    Email
    c-guillemare@chu-montpellier.fr
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Catherine Alix-Panabières, Ph.D.
    Organizational Affiliation
    University Hospital, Montpellier
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Thomas Bardol, M.D.
    Organizational Affiliation
    University Hospital, Montpellier
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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