RecruitingNCT07199959

Study on the Mechanism of Acquired Resistance of Entrectinib

A Multi-center Retrospective Study of the Mechanism of Acquired Resistance in First Line Treatment of ROS1fusion Positive NSCLC With Entrectinib


Sponsor

Fudan University

Enrollment

38 participants

Start Date

Jan 15, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

The goal of this observational study is to learn about the mechanism of acquired resistance in first line trearment of ROS1-positive NSCLC with entrectinib. The main question it aims to answer is: what is the acquired resistant mechanism of entrectinib as first line treatment setting in patients? Tissue or blood samples of participants who have already taken entrectinib as their regular medical care for NSCLC will send for Next gene sequencing for genomic profiles and bioinformatic analysis.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is investigating what causes resistance to entrectinib — a targeted therapy for non-small cell lung cancer with a ROS1 gene fusion — after it initially works. Researchers want to identify the biological changes that allow the cancer to start growing again, to guide future treatment strategies. **You may be eligible if...** - You are 18 or older with advanced non-small cell lung cancer (stage IIIB–IV) - Your cancer has a ROS1 gene fusion confirmed by molecular testing - You have not previously received systemic treatment for your advanced-stage cancer - You have at least one measurable tumor on imaging **You may NOT be eligible if...** - You have already been treated with systemic chemotherapy, immunotherapy, or targeted drugs for your advanced-stage disease - Your cancer does not have a confirmed ROS1 fusion - You do not have measurable disease 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

PROCEDUREvenipuncyure

venipuncture as clinical practical setting

DRUGEntrectinib

600mg, oral, once daily


Locations(1)

Fudan university shanghai cancer center

Shanghai, Shanghai Municipality, China

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NCT07199959