Non Small Cell Lung Cancer
Conditions
Brief summary
Early non-small cell lung cancer (NSCLC), treated by surgery or radiotherapy in the case of inoperability, relapses in almost 50% of cases. Circulating tumour cells (CTCs), which can be detected before surgery, represent a promising prognostic tool, but the markers characterising their aggressiveness remain to be determined. The NSCLC microenvironment, in which purinergic signalling is a key pathway, controls tumour development. Adenosine derived from the action of CD39 and CD73 ectonucleotidases hydrolysing extracellular ATP, induces immunosuppression of NSCLC by activating A2R receptors. The expression and prognostic relevance of A2R, CD39 and CD73 on CTCs is unknown. The objectives are to (i) compare the expression of A2R and CD39 and CD73 on primary tumour cells and CTCs of patients operated on for early NSCLC, (ii) correlate these data with molecular characteristics and clinical response, (iii) determine on lung cancer lines whether irradiation impacts on the expression of A2R, CD39 and CD73. This work could contribute to the identification of new theranostic biomarkers.
Interventions
Sample of whole blood and tissue for ex vivo expression of A2R, CD39, CD73 and P2RX7
Sponsors
Study design
Eligibility
Inclusion criteria
i) Inclusion criteria: * Patient of legal age (\>18 years), any gender, * operated on for stage (IA to IIB) non-small cell lung cancer (NSCLC) ii)
Exclusion criteria
* Patient with any other active cancer. * Lack of evaluable material.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Ex vivo expression of A2R (adenosine receptor), CD39, CD73 and P2RX7 on NSCLC and CTC | At inclusion | Presence versus Absence of expression (immunohistochemistry) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| In vitro impact of radiation therapy on the A2R, CD39, CD73 expression by cells lineage | At inclusion | Upregulation / Downregulation of expression (mRNA by real time PCR) |
Countries
France