Tumor Rebiopsy During Progression Under Immunotherapy for Patients With Lung Cancer
NCT04300062
Summary
The objective of the study aims to collect tumor tissue at the moment of progression under Immune checkpoint inhibitors (ICI) in biological resources center in Ambroise Paré hospital, in order to insure later study on molecular mechanism involving the progression of NSCLC and SCLC under ICI. The further analysis of research will be performed in the EA 4340 unity, Biomarkers and Clinical Trials in cancerology and onco-hematology, UVSQ, University of Paris-Saclay.
Eligibility
Inclusion Criteria: * Diagnosed NSCLC or SCLC; * Patient treated priorly by ICI and progressed under ICI; * Have provided written informed consent for the study; * Be \>/= 18 years of age on day of signing informed consent. Exclusion Criteria: * Patient under guardianship or curatorship; * Unable to provide written informed consent for the study; * Technical impossibility to carry out tissular rebiopsy under local anesthesia.
Conditions2
Browse More Trials
Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.
NCT04300062