RecruitingNot ApplicableNCT06247826

Mechanisms of Resistance to Amivantamab in Patients With NSCLC With EGFR Exon 20 Insertion


Sponsor

Groupe Francais De Pneumo-Cancerologie

Enrollment

30 participants

Start Date

Jan 15, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this prospective, interventional study is to evaluate the mechanisms of acquired resistance to amivantamab monotherapy in patients with advanced NSCLC with EGFR ins20. The main question it aims to answer is: What are the mechanisms of acquired resistance to amivantamab monotherapy in this population of patients ? How anticipate the efficacy of subsequent systemic therapies ? After this information session, the participant will be asked to sign the study informed consent. A blood samples (2\*10 mL on ethylenediaminetetraacetic acid (EDTA)) will be taken at time of disease progression and will be sent for central liquid biopsy ctDNA analysis. If available, tumor tissue will also be sent for DNA NGS analysis.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study investigates why some lung cancers stop responding to a drug called amivantamab. It focuses on patients with non-small cell lung cancer (NSCLC) who have a specific genetic change called an EGFR exon 20 insertion. Researchers will collect blood and tissue samples to understand how the cancer develops resistance. **You may be eligible if...** - You are 18 or older - You have advanced non-small cell lung cancer with the EGFR exon 20 insertion mutation - You are currently receiving amivantamab as a single treatment (not combined with other drugs) in France - Your cancer has progressed while on amivantamab - You are enrolled in the French national health insurance program **You may NOT be eligible if...** - You are receiving amivantamab combined with another treatment - You are not willing to provide blood samples - You are not in France's healthcare system Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREBlood sampling

Blood samples (2\*10 mL on ethylenediaminetetraacetic acid (EDTA)) will be taken at time of disease progression and will be sent for central liquid biopsy ctDNA analysis.


Locations(18)

Oncologie Polyclinique Bordeaux Nord Aquitaine

Bordeaux, France

Centre Hospitalier du Morvan

Brest, France

Pneumologie Centre Hospitalier Intercommunal de Créteil

Créteil, France

Oncologie, CLCC Dijon

Dijon, France

Pneumologie, CHU Grenoble

Grenoble, France

Pneumologie CH

Le Mans, France

Oncologie thoracique Hôpital Nord

Marseille, France

Oncologie, Centre Antoine Lacassagne

Nice, France

Oncologie Institut Curie

Paris, France

Hôpital Cochin

Paris, France

Pneumologie, Hôpital Tenon

Paris, France

Pneumologie Centre Hospitalier

Pau, France

Pneumologie CHI Cornouaille

Quimper, France

Hôpital Charles Nicolle

Rouen, France

CHU La Réunion Site Nord

Saint-Denis, France

CHU Hôpital Nord

Saint-Etienne, France

CH Bretagne Atlantique

Vannes, France

Pneumologie, Hôpital Mutualiste Resamut

Villeurbanne, France

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NCT06247826


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