LUNGadenosine: A2R and Ectonucleotidases Expression in Lung Cancer Circulating Tumor Cells

Sponsor
Centre Hospitalier Universitaire de Nice (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05648188
Collaborator
(none)
60
1
21.9
2.7

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Biological: Sample

Study Design

Study Type:
Observational
Anticipated Enrollment :
60 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Assessing the Expression of A2R Receptors and CD39 and CD73 Ectonucleotidases on Circulating Tumour Cells of Non-small Cell Lung Carcinoma
Anticipated Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Oct 30, 2024
Anticipated Study Completion Date :
Oct 30, 2024

Arms and Interventions

Arm Intervention/Treatment
NSCLC patients

Patients with proven stage IA-IIB non-small cell lung cancer (NSCLC).

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

Outcome Measures

Primary Outcome Measures

  1. Ex vivo expression of A2R (adenosine receptor), CD39, CD73 and P2RX7 on NSCLC and CTC [At inclusion]

    Presence versus Absence of expression (immunohistochemistry)

Secondary Outcome Measures

  1. 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)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
  1. Inclusion criteria:
  • Patient of legal age (>18 years), any gender,

  • operated on for stage (IA to IIB) non-small cell lung cancer (NSCLC)

  1. Exclusion criteria:
  • Patient with any other active cancer.

  • Lack of evaluable material.

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU de Nice Nice France 06001

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Nice

Investigators

  • Principal Investigator: Jonathan BENZAQUEN, Dr, Centre Hospitalier Universitaire de Nice

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Nice
ClinicalTrials.gov Identifier:
NCT05648188
Other Study ID Numbers:
  • 22Pneumo01
First Posted:
Dec 13, 2022
Last Update Posted:
Dec 13, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 13, 2022