MedPath

Identification by Microarrays of the Risks of Metastatic Relapse, Toxicity and Resistance to Adjuvant Chemotherapy in Completely Resected Non-small Cell Lung Cancer

Conditions
Non-small Cell Lung Cancer
Registration Number
NCT02075957
Lead Sponsor
University Hospital, Angers
Brief Summary

Description of new transcriptional profiles associated with risk of relapse and identification of specific sites of relapse in non-small cell lung cancer, toxicity and resistance to adjuvant chemotherapy in completely resected non-small cell lung cancer (NSCLC).

Detailed Description

* A first blood sample will be taken during the week before the operation. A second blood sample will be taken 4 to 8 weeks after the operation. And in case of relapse, a third sample will be taken. These samples are going to be stored in the collection of biological resources of Angers.

* Concerning the biopsy of the resected NSLCL, it will be sent to the collection of biological resources of Angers for conservation directly next to the surgery.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
192
Inclusion Criteria
  • Major subject
  • Subject who received resection with primary non-small cell lung cancer at the University Hospital of Angers and whose tumor samples will be stored in collection of biological resources of University Hospital of Angers
  • A written inform consent.
Exclusion Criteria
  • Under 18 year old;
  • Pregnant or nursing women;
  • Deprived of liberty;
  • Age under curatorship or guardianship;
  • Unable to consent person;
  • About not carrying a non-small cell lung cancer.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Determination of news microarrays profiles of NSCLC relapse risksAt 10 years

The news microarrays profiles of NSCLC relapse risks will :

* assessing the risk of relapse in patients undergoing resection of NSCLC (by knowing this risk, patients at highest risk of relapse would be treated as a priority, while avoiding treating patients with low risk)

* assessing the risk of chemo-resistant tumor cells characters to optimize the choice of treatment to offer to the patient

* assessing the prediction of sites most likely metastatic relapse to guide survey strategy.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

UH Angers

🇫🇷

Angers, Maine et Loire, France

© Copyright 2025. All Rights Reserved by MedPath