RecruitingNot ApplicableNCT05033691

A Study to Evaluate the Efficacy of Osimertinib With Early Intervention SRS Treatment Compared to the Continuation of Osimertinib Alone, in Patients With EGFR Mutated NSCLC and Asymptomatic Brain Metastases

A Multi-center, Open-label, Randomized, Two-arm Study, to Evaluate the Efficacy of Osimertinib With Early Intervention SRS Treatment Compared to the Continuation of Osimertinib Alone, in Patients With EGFR Mutated NSCLC and Asymptomatic Brain Metastases.


Sponsor

Hadassah Medical Organization

Enrollment

162 participants

Start Date

Mar 9, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

This study involves patients with EGFR-mutated NSCLC and asymptomatic brain metastases. This is an open-label, randomized study, comparing the continuation of Osimertinib treatment alone to Osimertinib treatment combined with early intervention stereotactic radiosurgery (SRS). The current first line of care for EGFR-mutated NSCLC is administration of Osimertinib, a small molecule that penetrates the blood brain barrier (BBB) well and controls majority, but not all, of the brain metastases. We hypothesize that relatively early intervention with SRS to brain metastases that are still visualized by MRI 2 months-post initiation of Osimertinib treatment, LUNG- will improve long term brain control, cognitive abilities and potentially overall survival. Patients with EGFR-mutated NSCLC and asymptomatic brain metastases will be treated with Osimertinib for 2 months. Brain MRI scans will be collected pre-Osimertinib and 2 months after treatment start. Patients with asymptomatic brain metastases present after 2 months of Osimertinib will be randomized into one of two study arms. Arm A patients will be treated with SRS while continuing Osimertinib, while arm B patients will continue with Osimertinib alone. Patients will be assessed based on brain and whole body progression by RECIST. Patients will also be assessed for CNS-PFS and body-PFS, cognitive function, Quality of life and overall survival status via routine follow-up tests.


Eligibility

Min Age: 18 YearsMax Age: 120 Years

Plain Language Summary

Simplified for easier understanding

This trial tests whether adding early stereotactic radiosurgery (SRS — a precise form of focused radiation) to the drug osimertinib improves outcomes for people with lung cancer that has spread to the brain. Osimertinib is a targeted pill for a specific genetic mutation (EGFR) in non-small cell lung cancer (NSCLC). The brain metastases must be small and causing no or minimal symptoms. **You may be eligible if...** - You are 18 or older - You have newly diagnosed metastatic non-small cell lung cancer with an EGFR mutation - Your cancer has spread to the brain (fewer than 20 brain lesions), and these are asymptomatic or causing only minor symptoms - You are starting osimertinib as your EGFR-targeted therapy - You are eligible for stereotactic radiosurgery - You are in generally good health (ECOG 0–2) **You may NOT be eligible if...** - You have more than 20 brain lesions at the time of randomization - Your brain metastases are causing significant symptoms - You are not eligible for SRS treatment - You do not have an EGFR mutation sensitive to osimertinib 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.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

RADIATIONStereotactic surgery

At two month (8 weeks) post Osimertinib start, patients will be randomized into one of the two study arms. Arm A patients will be treated with stereotactic surgery (SRS). In both arms Osimertinib treatment will continue.


Locations(1)

Hadassah Ein Kerem Medical Center

Jerusalem, Israel

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05033691


Related Trials