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NCT05044676: IMMUNOCELL

Immune Cells as a New Biomarker of Response in Patients Treated by Immunotherapy for Advanced Hepatocellular Carcinoma

Terminated Last updated 18 December 2025
What this trial tests

trial testing patients with hepatocellular carcinoma in Hepatocellular Carcinoma in 4 participants. Terminated before completion.

Timeline
8 September 2023
Primary endpoint
22 September 2025
22 September 2025

Quick facts

Lead sponsorAssistance Publique - Hôpitaux de Paris
StatusTerminated
Study typeOBSERVATIONAL
Enrollment4
Start date8 September 2023
Primary completion22 September 2025
Estimated completion22 September 2025
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Assistance Publique - Hôpitaux de Paris — full company profile →

Who can join

Adults 18 to 90, any sex, with Hepatocellular Carcinoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Hepatocellular carcinoma (HCC) is the third leading cause of cancer death worldwide. Treatment options for advanced HCC remain very limited. Until recently, multikinase inhibitor were the gold standard for advanced hepatocellular carcinoma but associated with poor outcome and important side effects. Recently, the positive results of the Imbrave 150 study (a randomized study comparing Atezolizumab + Bevacizumab versus Sorafenib) prompted us to redefine our management strategy for advanced hepatocellular carcinoma by proposing the combination of Atezolizumab/Bevacizumab as treatment first-line in patients with advanced hepatocellular carcinoma. However, only 1/3 of the patients will respond to the combination of treatment and identifying predictive factors of response and new immune checkpoint inhibitors in order to target more tumors appear as a major issue. In this context, recent work has underlined the importance of the activating CD226/DNAM-1 receptor as an original immunotherapeutic target in various cancers (solid and hematopoietic tumors). CD226 is a transmembrane receptor that is part of the immunoglobulin superfamily. It is expressed by most T lymphocytes (CD8+, CD4+), by Natural Killer (NK) cells, by promoting their cytotoxicity. The investigators propose to prospectively analyze the frequency and phenotype (expression of CD226) of circulating immune cells before the initiation of treatment with Atezolizumab/Bevacizumab, 3 weeks after the first injection and its variation to determine whether this biomarker could predict the response to the treatment.

Publications & conference data

4 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Biomarkers and prognostic factors of PD-1/PD-L1 inhibitor-based therapy in patients with advanced hepatocellular carcinoma.
    Zhang N, Yang X, Piao M, Xun Z, et al · · 2024 · cited 69× · PMID 38355603 · DOI 10.1186/s40364-023-00535-z
  2. Immunotherapy in liver cancer: overcoming the tolerogenic liver microenvironment.
    Liu Y, Yang H, Li T, Zhang N. · · 2024 · cited 23× · PMID 39295859 · DOI 10.3389/fimmu.2024.1460282
  3. Liquid biopsy to identify biomarkers for immunotherapy in hepatocellular carcinoma.
    Ao H, Xin Z, Jian Z. · · 2021 · cited 17× · PMID 34930486 · DOI 10.1186/s40364-021-00348-y
  4. The Tumor Microenvironment of Hepatocellular Carcinoma: Untying an Intricate Immunological Network.
    Volponi C, Gazzillo A, Bonavita E. · · 2022 · cited 10× · PMID 36551635 · DOI 10.3390/cancers14246151

Verify or expand the search:

Other recruiting trials for Hepatocellular Carcinoma

Currently open trials in the same condition.

Other Assistance Publique - Hôpitaux de Paris trials

Trials by the same sponsor.

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Data sources for this page

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