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Tumor Rebiopsy During Progression Under Immunotherapy for Patients With Lung Cancer (REBIMMUNE)

A

Assistance Publique - Hôpitaux de Paris

Status

Enrolling

Conditions

Lung Cancer

Treatments

Procedure: Rebiopsy

Study type

Interventional

Funder types

Other

Identifiers

NCT04300062
APHP200398

Details and patient eligibility

About

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.

Full description

The study will consist of creation a tumor tissue bank, all sampling will be stored in the biological resources center of Ambroise Paré hospital.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Rebiopsy
Experimental group
Treatment:
Procedure: Rebiopsy

Trial contacts and locations

1

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Central trial contact

Etienne Giroux Leprieur, MD, PhD

Data sourced from clinicaltrials.gov

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