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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05648188
Other study ID # 22Pneumo01
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 1, 2023
Est. completion date October 30, 2024

Study information

Verified date December 2022
Source Centre Hospitalier Universitaire de Nice
Contact Jonathan BENZAQUEN, Dr
Phone 492038052
Email benzaquen.j@chu-nice.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date October 30, 2024
Est. primary completion date October 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Intervention

Biological:
Sample
Sample of whole blood and tissue for ex vivo expression of A2R, CD39, CD73 and P2RX7

Locations

Country Name City State
France CHU de Nice Nice

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nice

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ex vivo expression of A2R (adenosine receptor), CD39, CD73 and P2RX7 on NSCLC and CTC Presence versus Absence of expression (immunohistochemistry) At inclusion
Secondary In vitro impact of radiation therapy on the A2R, CD39, CD73 expression by cells lineage Upregulation / Downregulation of expression (mRNA by real time PCR) At inclusion
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