Lung cancer trial questions need for immediate brain radiation in asymptomatic patients
NCT ID NCT05236946
First seen Jun 24, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This Phase 3 trial is testing whether it is safe to delay brain radiotherapy in lung cancer patients with specific genetic mutations (EGFR/ALK) who have asymptomatic brain metastases. Participants will receive standard targeted therapy (TKI) and be randomly assigned to either immediate brain radiation or observation with radiation only if symptoms develop. The study aims to see if delaying radiation can maintain brain tumor control while avoiding unnecessary side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Tyrosine kinase inhibitor (TKI) and brain radiotherapy (stereotactic radiosurgery or whole brain radiotherapy)
- What this could lead to
- If successful, this could show that delaying brain radiotherapy is safe for patients with asymptomatic brain metastases, allowing them to avoid side effects while still controlling the disease.
- What could go wrong
- This is a relatively small Phase 3 trial (190 participants) and results may not apply to all lung cancer types. There is a risk that delaying radiotherapy could lead to worse brain tumor control.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 190 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2020
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 99 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥ 18 years 2. Patients with ECOG performance status of 0-2 3. Patients with pathologically proven diagnosis of NSCLC 4. Patients with positive oncogene mutation status (EGFR/ALK) 5. Patients with radiologically confirmed parenchymal brain metastases 6. Patients with asymptomatic Synchronous or Metachronous brain metastases 7. Patients willing for written informed consent and must be willing to comply with the specified follow-up schedule Exclusion Criteria: 1. Patients with CSF dissemination only without any parenchymal brain metastases 2. Patients with brain metastases in the brain stem 3. Patients with prior history of radiation therapy to the brain 4. Patient not suitable for TKI therapy as per the medical oncologist 5. Pregnant or lactating females
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Tata Memorial Hospital
RECRUITINGMumbai, Maharashtra, 400012, India