New combo radiation therapy aims to tame large brain tumors
NCT ID NCT07162246
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tests a new way to treat large brain tumors using two different radiation machines. Patients get four daily treatments with a linear accelerator, then a break, followed by one precise Gamma Knife treatment. The goal is to better control tumors while protecting healthy brain tissue. The trial will enroll 60 adults with up to two large brain lesions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Radiation therapy (Gamma Knife and linear accelerator)
- What this could lead to
- If successful, this could offer a safer, more effective way to treat large brain tumors, reducing side effects like radiation necrosis.
- What could go wrong
- This is a small, early-phase trial (60 people) testing a new combination. It may not work better than current methods, and there are still risks of side effects.
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 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Jun 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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 years and older
- 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: * Presence of up to two large intracranial lesions * Up to 10 (previously untreated, or progressing after previous treatment) brain metastases at the time of enrollment on the diagnostic MRI (which includes the ILLs) to be treated with SRS/HSRS * Age =\> 18 years * Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 * Expected survival \>3 months * Patients that are deemed suitable for both GK and Linac based treatment * Patients that are able to hold systemic cancer chemotherapy/immunotherapy at least 2 days prior and following an SRS fraction Exclusion Criteria: * Prior SRS to the ILLs * Prior WBRT, or plan for concurrent WBRT with the protocol treatment * Presence or history of any leptomeningeal/pachymeningeal disease * Metastatic disease within the ventricles of the brain or corpus callosum * Small cell, hematopoietic or germ cell primaries * Patient with absolutely contraindications for MRI * Severe symptoms that preclude MRI or treatment using standard procedures for Linac or GK * Pregnant or lactating patient * Inability or unwillingness to undergo informed consent or post-treatment follow-up
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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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Sunnybrook Health Sciences Centre
RECRUITINGToronto, Ontario, M4N3M5, Canada
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