The objective is to study the phenotypic, functional and metabolomic characteristics of neutrophils circulating subpopulations in lung cancer patients, and to compare them to a control group of healthy volunteers. A blood sample will be taken before the first treatment session for the lung cancer patient and a second blood sample will be taken during the first evaluation visit. The investigators hypothesize that there may be different circulating neutrophil subpopulations in patients with metastatic non-small cell lung cancer (NSCLC) involved in tumor progression and resistance to immunotherapy.
Immune checkpoint inhibitors (ICI) have been shown to be effective in metastatic lung cancer. Unfortunately, 80% of patients do not respond and show rapid disease progression. Identifying predictive biomarkers of response is essential for early adaptation of management. Circulating lymphocytes and neutrophils represent a biomarker (NLR), predictive of immunotherapy response, in particular via the measurement of the neutrophils /lymphocyte ratio. Some preclinical work suggests a role for circulating neutrophil subpopulations like MDSC (myeloid derived suppressor cells) in ICI resistance. Certain circulating neutrophil subpopulations are thought to promote tumor progression, angiogenesis and metastasis with immunosuppressive activity. Identifying these pro-tumor subpopulations could predict the response to ICI and could be a potential therapeutic target. Our goal is to characterize the circulating neutrophil subpopulations of lung cancer patients and correlate these characteristics with response and survival phenotypically and functionally.
Study Type
OBSERVATIONAL
Enrollment
100
Extra blood tubes
Assistance Publique - Hôpitaux de Paris (AP-HP) - Cochin Hospital - Pneumology unit
Paris, Île-de-France Region, France
RECRUITINGPresence of a subpopulation of circulating neutrophils
Presence of a subpopulation of circulating neutrophils in patients with lung cancer (absent in healthy volunteers and COPD patients) with phenotypic CD45+, CD15+, CD16+, CD62L-, LOX1+ and functional immunosuppressive characteristics.
Time frame: Through study completion, an average of 3 years
Demographic characteristics
Demographic characteristics : age, sex and smoking
Time frame: Day 1
Performans status
Somatic characteristics
Time frame: Day 1
Stage
Somatic characteristics
Time frame: Day 1
Histologic type
Histologic characteristics
Time frame: Day 1
Mutation status
Molecular characteristics
Time frame: Day 1
Clinical assessment
Progression free survival (defined as the time between the start of treatment and the date of first observation of clinical or CT progression (irRECIST1.1 criterion) or death)
Time frame: Up to the end of participation, between month 3 and month 4
irRECIST 1.1 response
CT scan to evaluate progression free survival (defined as the time between the start of treatment and the date of first observation of clinical or CT progression (irRECIST1.1 criterion) or death)
Time frame: Up to the end of participation, between month 3 and month 4
Death
Progression free survival (defined as the time between the start of treatment and the date of first observation of clinical or CT progression (irRECIST1.1 criterion) or death)
Time frame: Up to the end of participation, between month 3 and month 4
Mortality
Overall survival (defined as the time from treatment diagnosis to the date of death).
Time frame: Up to the end of participation, between month 3 and month 4
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