Characterisation of TLR4+ Blood Cells in Patients With Solid Cancer (ODYSSEE)

The potential of immunotherapy in the treatment of cancer is now well documented. While excessive activation of the immune system may be associated with severe reactions and/or auto-immune syndromes, it is now clearly established that controlled activation of the adaptive immune system constitutes a major contribution to the treatment of cancer. Antigen-independent activation of the adaptative immune system with " immune checkpoint inhibitors " (ICI) has allowed prolonged survival in a minority of patients with previously intractable disease. However, a variety of tumor indications are still presently inaccessible to immunotherapeutic approaches or poorly responsive to these therapies.

The immune system is a highly reactive complex comprising antigen-specific cells (adaptive immune system) and antigen-agnostic cells (innate immune system) which interact closely in a complex network. The adaptive immune response is mediated by B and T cells upon antigen-specific recognition. The innate response is mediated by macrophages, dendritic cells, Natural Killer cells and assume the immediate defense of the organism against infectious agents. The innate immune system plays a key role in antigen processing and presentation, production of key cytokines and as anti-tumor effector cells. The role of the innate immune system in the control of cancer progression and in cancer therapy is well documented. Natural Killer cells, involved in antibody-dependent cellular cytotoxicity, and cells performing phagocytosis such as macrophages and neutrophils, participate in tumor destruction after intervention of adaptive immune cells and in combination with certain tumor-targeting therapies, such as antibodies recognizing tumor-specific antigens.

The Odyssey project aims to harness the next generation paradigm of cancer immunotherapy : systemic stimulation of the innate immune system.

To achieve this endeavour the investigator will exploit a well-known yet poorly documented phenomenon, i.e. the rare occurrence of cure in cancer patients who have presented a simultaneous severe septic episode at the time of diagnosis.

Several clinical studies have been realized in order to demonstrate the effect of the innate immune response activation by the bacterial LPS (lipopolysaccharides) in cancer therapy. However, severe toxicities have been described even at very low dose of LPS. The LPS-activated immune response is mediated by TLR4 (Toll Like Receptor 4), a transmembrane receptor expressed by several cell types including monocytes and macrophages. The interaction of TLR4 with LPS mainly induces the release of proinflammatory cytokines (so called " canonical pathway "). TLR4-signalling cascade can also induce the release of type I interferon (so called " alternative pathway "), a class of cytokines known to promote antitumoral activity. LPS tolerance is presumed to be rather associated with the activation of the alternative pathway. Therefore, managing this LPS tolerance is a key mechanism that could limit the systemic toxicity of LPS while stimulating the innate immune system.

Héphaïstos-Pharma biotech and the CRCL Onco-Pharmacology lab (Centre de Recherche en Cancérologie de Lyon) have set up a modified formulation of the LPS that improves its pharmacokinetic properties, reduces its toxicity, and preferentially activates TLR4-alternative signalling pathway. Before investigating the effect of this new immunostimulant in a future phase I/II clinical trial, a translational study is required to further characterize the TLR4 positive cells population as well as the innate immune system in patients with solid cancer.

Study Overview

• Status: Recruiting
• Conditions: All Types of Solid Cancer
• Intervention / Treatment: Biological: Blood sampling; Biological: Blood sampling

• Study Type: Interventional
• Enrollment (Estimated): 300
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Charles DUMONTET, MD; Phone Number: 33 06 82 13 66 14; Email: charles.dumontet@chu-lyon.fr
• Study Contact Backup: Name: Angelique STUANI; Phone Number: 33 04 78 86 23 76; Email: angelique.stuani@chu-lyon.fr

Study Locations

• France
  • Bron, France, 69500
    • Recruiting
    • Pneumology Unit
    • Contact: Michael DURUISSEAUX, MD; Phone Number: 33 04 72 35 76 44; Email: michael.duruisseaux@chu-lyon.fr
  • Pierre Benite, France, 69495
    • Recruiting
    • Oncology Unit, Hospices Civils de Lyon Sud
    • Contact: Benoit YOU, MD; Phone Number: 33 04 78 86 43 53; Email: Benoit.you@chu-lyon.fr
  • Pierre-Bénite, France, 69495
    • Recruiting
    • Dermatology Unit
    • Contact: Stephane DALLE, MD; Phone Number: 33 04 78 86 16 28; Email: stephane.dalle@chu-lyon.fr
  • Pierre-Bénite, France, 69495
    • Recruiting
    • Oncological and Gynecological Surgery Unit,
    • Contact: François GOLFIER, MD; Phone Number: 33 04 78 86 41 78; Email: francois.golfier@chu-lyon.fr

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Patient older than 18 years
• Patient who gave its written informed consent to participate to the study
• Patient with histologically confirmed diagnosis of any type of malignancy (solid tumors)
• Patient with a minimum of 6 months life expectation at inclusion
• Patient covered by a medical insurance

Inclusion criteria specific to cohort 1:

- Patient with metastatic disease or unresectable locally advanced malignancy (solid tumors) who is naive of immune checkpoint inhibitors (ICI)-based immunotherapy and is due to initiate an ICI immunotherapy alone or in combination with any other systemic anticancer treatment.

Inclusion criteria specific to cohort 2:

- Patient with a diagnosed malignancy amenable to surgery with curative intent who is naive of any anticancer treatment

Exclusion Criteria:

• Patient with secondary malignancy unless this malignancy is cured with no evidence of recurrence for at least 5 years.
• Pregnant or breastfeeding woman or expecting to conceive
• Patient who is deprived of liberty due to judicial or administrative decision
• Patient with known psychiatric disorders that would interfere with cooperation with the requirements of the trial
• Patient admitted in a social or sanitary institution for an objective other than the one of this trial
• Adult patient under legal protection

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Screening
• Allocation: Non-Randomized
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Immunotherapy; Patients with locally advanced/metastatic disease who are due to receive as a first attempt an immune checkpoint inhibitors immunotherapy-based treatment. Blood sample collection : One blood draw of 10 mL will be realized before the initiation of immunotherapy. Any adverse event related to the blood draw will be recorded. A follow-up will be performed at 6 months to record the immune-related adverse events, a statement of the disease and any other cancer treatments received. A 24 months long term follow up will be performed to record patient vital status and any date of disease progression.	Biological: Blood sampling; One blood sample of 10mL is realized before initiation of immunotherapy; Biological: Blood sampling; Three blood samples of 10mL are realized at distinct steps of patients disease management : one before the curative surgery, one after three months and one after six months.
Other: Curative surgery; Patients newly diagnosed and naive of any anticancer treatment who are due to receive a curative surgery of their primitive tumor. Blood samples collection : Three blood draws of 10 mL will be realized : one before the surgery, one after 3 months and one after 6 months. Any adverse event related to the blood draw will be recorded. A follow-up will be performed at 6 months to record the statement of the disease and any other cancer treatments received. A 24 months long term follow up will be performed to record patient vital status and any date of disease relapse.	Biological: Blood sampling; One blood sample of 10mL is realized before initiation of immunotherapy; Biological: Blood sampling; Three blood samples of 10mL are realized at distinct steps of patients disease management : one before the curative surgery, one after three months and one after six months.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Cohort 1 : 24 months-progression free survival (24M PFS)	Cohort 1 : 24M-PFS defined as the time from the date of the first drug administration to the first documented clinical, biological or radiological progression according to investigator assessment during a period of 24 months. Patients who have not progressed at the time of analysis will be censored at the time of the latest date of assessment.	24 months
Cohort 2 : describe the evolution of the percentage of TLR4+ cells in peripheral blood after curative ablation of a cancerous tumour.	Number of TLR4 positive cells before curative surgery and after 3 and 6 months.	Before surgery, after 3 months and after 6 months.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Overall Survival (OS) Cohorts 1 and 2	OS defined as the time from the date of the day of the treatment to the date of death due to any cause. Any patient not known to have died at the time of analysis will be censored based on the last recorded date on which the patient was known to be alive.	Baseline,date of death, last recorded date or 24 months
Concentration of innate and adaptive immune cell population Cohorts 1 and 2	Concentration of innate and adaptive immune memory cells in peripheral blood as defined by the expression level of specific immunophenotypic cell surface receptors	Baseline
LPS-mediated activation of TLR4 positive cells Cohorts 1 and 2	LPS-mediated activation of TLR4 positive cells defined as the expression of the membrane marker CD169	baseline
Number of high grade (≥3) immune-related adverse events (irAE) Cohort 1	Number of high grade (≥3) irAE(s) 6 months after initiation of immunotherapy	Baseline ans 6 month
24 months-relapse free survival (24M RFS) Cohort 2	24M-RFS defined as the time from the date of the surgery to the first documented clinical, biological or radiological progression according to investigator assessment during a period of 24 months. Patients who have not relapsed at the time of analysis will be censored at the time of the latest date of assessment.	Before surgery, after 3 months, after 6 months and after 24 month

Collaborators and Investigators

• Sponsor: Hospices Civils de Lyon

Study record dates

Study Major Dates

• Study Start (Actual): May 29, 2024
• Primary Completion (Estimated): May 1, 2028
• Study Completion (Estimated): May 1, 2028

Study Registration Dates

• First Submitted: October 13, 2023
• First Submitted That Met QC Criteria: November 8, 2023
• First Posted (Actual): November 14, 2023

Study Record Updates

• Last Update Posted (Actual): May 18, 2025
• Last Update Submitted That Met QC Criteria: May 14, 2025
• Last Verified: May 1, 2025

More Information

Terms related to this study

• Keywords: Immunotherapy; Immunostimulant; Lipopolysaccharides; Innate immune system systemic activation; TLR4 positive immune cells
• Other Study ID Numbers: 69HCL23_0596; 2023-A01542-43 (Other Identifier: ID-RCB)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No