Trials / Withdrawn
WithdrawnNCT05648188
A2R and Ectonucleotidases Expression in Lung Cancer Circulating Tumor Cells
Assessing the Expression of A2R Receptors and CD39 and CD73 Ectonucleotidases on Circulating Tumour Cells of Non-small Cell Lung Carcinoma
- Status
- Withdrawn
- Phase
- —
- Study type
- Observational
- Enrollment
- 0 (actual)
- Sponsor
- Centre Hospitalier Universitaire de Nice · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | Sample | Sample of whole blood and tissue for ex vivo expression of A2R, CD39, CD73 and P2RX7 |
Timeline
- Start date
- 2023-01-01
- Primary completion
- 2024-10-30
- Completion
- 2024-10-30
- First posted
- 2022-12-13
- Last updated
- 2025-04-10
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT05648188. Inclusion in this directory is not an endorsement.