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Starting soon Not applicable

Effect of G-CSF on MDSC and Cancer Stem-cells Interactions in Non-small Cell Lung Cancers (CIRCUIT)

NCT06711770 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-12
Last updated
2025-07-30

Condition(s) studied

Non Small Cell Lung CancerImmunotherapyGranulocyte Colony Stimulating Factor

Investigational drug(s) / intervention(s)

Blood sample →

Blood sample: Four tubes of 7 mL collected at baseline, 3 weeks, 6 weeks, 12 weeks, 6 months, 12 months and 24 months (end of chemo-immunotherapy) or in case of relapse

Study summary

Immunotherapy have revolutionized the field of oncology, but response rates are low and all patients relapse, due to immunologic (myeloid immunosuppressive cells) and non-immunologic (cancer stem- cells (CSC)) mechanisms. CSC are able to circulate within blood, protected from destruction by immunosuppressive cells such as MDSC. Some factors such as G-CSF, administered to lower febrile neutropenia, should modulate properties of MDSC and CSC, but data are contradictory, and literature remain poor regarding its effects on the interactions between MDSC and CSC in blood clusters. Indeed, this project aims at better characterizing the effect of G-CSF on these interactions and on their functions in NSCLC patients receiving G-CSF.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients (male or female) aged ≥ 18 years * Histological or cytological proven lung adenocarcinoma, metastatic or locally advanced not accessible to local therapy * Receiving chemotherapy and immunotherapy as first-line treatment * Signed written informed consent (no later than the day of inclusion, and before the blood sample collection) * Patient affiliated or beneficiary to a health security system; Exclusion Criteria: * Patient with a small cell lung carcinoma * Non-metastatic disease * Actionable mutation or genomic alteration in EGFR, ALK or ROS1 * Corticosteroids \> 10 mg/j * Autoimmune disease * Active and uncontrolled HIV infection * Concomitant cancer * Pregnancy or lactating women * Psychiatric or medical conditions that prohibit the understanding and rendering of informed consent * Patient under a legal protection measure * Patient with a deprived liberty condition * Patient incapable of giving signed informed consent * Patient within the exclusion period for another clinical trial, or participating to another interventional trial within 30 days before the beginning of this project

Primary outcome measure(s)

  • Phenotype of MDSC and CSC — At baseline, 3 weeks, 6 weeks, 12 weeks, 6 months, 12 months and 24 months (end of chemo-immunotherapy) or in case of relapse
    Expression of different MDSC markers corresponding to the rate of the different MDSC subpopulations
  • Functions of MDSC and CSC — At baseline, 3 weeks, 6 weeks, 12 weeks, 6 months, 12 months and 24 months (end of chemo-immunotherapy) or in case of relapse
    Immunosuppressive and non immunosuppressive functions of the different populations of MDSC

Trial sites (1)

FacilityCityRegionStatus
CHU de Bordeaux, service d'Oncologie Médicale Bordeaux France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06711770 on ClinicalTrials.gov ↗ ← All trials in France