Can targeted radiation retrain recurrent brain tumors?
NCT ID NCT05081908
First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time
Summary
This trial tests whether multisession radiosurgery, a type of focused radiation delivered in several sessions using the Cyberknife system, can safely control atypical meningiomas that remain or come back after surgery. The study enrolls adults with grade II meningiomas who have residual or recurrent tumors. Researchers will track neurological side effects and measure tumor response using MRI scans to see if the treatment stabilizes or shrinks the lesions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Multisession radiosurgery (hypofractionated radiotherapy) delivered with Cyberknife
- What this could lead to
- If it works, this approach could offer a safe way to control atypical meningiomas that remain or return after surgery, potentially delaying the need for more invasive treatments.
- What could go wrong
- This is a small feasibility study, so results may not apply broadly. The treatment may cause neurological side effects, and it is not yet clear how well it controls tumor growth over the long term.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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25 people
The number who actually took part.
- Started
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May 2017
- Finished
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May 2023
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients had residual or recurrent atypical meningioma (grade II) after surgery (Simpson score) * Age: ≥ 18 years old * Karnofsky performance Status ( KPS) ≥ 70 * Written consent Exclusion Criteria: * Pregnancy * Neurofibromatosis type 2 (NF2) * Concomitant aggressive haematological or solid neoplasm
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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.
Contacts and locations
Locations
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UOC Radioterapia
Milan, Milano, 20133, Italy
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