Brain Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People aged 18 or older
- People who have signed and dated a consent form and are willing to follow all study procedures for the full duration of the trial
- People whose general health and ability to carry out daily activities meets a minimum level, as measured by a standard medical scoring scale called the Karnofsky scale (score of 60 or above)
- People who have a confirmed cancer diagnosis (either a primary tumour or one that has spread from elsewhere in the body), based on tissue testing
- People who are able to take steroid medications
- People who are able to have an MRI scan (no medical reasons preventing this)
- People whose MRI scan shows a clearly defined, contrast-enhancing brain metastasis no larger than 4.0 cm that a specialist tumour board has recommended for surgical removal, and who have no more than 3 other brain metastases that could be treated with a focused type of radiation therapy
- People whose treating doctor estimates they have a life expectancy of more than 12 months
- People whose blood test results meet minimum levels for platelets, clotting function, and haemoglobin (confirm specific values with trial site)
Who may not be able to join:
- People whose cancer is of a type known as radiosensitive — specifically germ cell tumour, lymphoma, or multiple myeloma
- People showing signs of significant pressure building inside the skull that would require urgent surgery (such as a midline shift greater than 10 mm or compression of certain brain structures)
- People with more than 4 brain metastases in total, or whose metastasis being considered for removal is larger than 4.0 cm
- People who have more than one brain metastasis that would require surgical removal
- People with cancer that has spread to the lining or fluid surrounding the brain or spinal cord (unless it is in a limited area that can be treated with radiation at the same time as the surgery)
- People who have previously received radiation treatment to the brain, including focused radiation to the specific lesion being considered or whole-brain radiation
- People who have previously had surgery to remove a brain tumour (whether primary or secondary)
- People who have previously been diagnosed with a brain tumour other than a meningioma
- People who have received a radioactive (radionuclide) therapy within the past 30 days
- People who have received a type of cancer therapy targeting blood vessel growth (anti-VEGF therapy) within the past 6 weeks
- People who are unable to tolerate the positioning and treatment involved in focused radiation therapy
- People who are unable to give informed consent
- People who are pregnant or breastfeeding
- Women of reproductive potential who are not willing to use effective contraception for at least 6 months after radiation treatment
- Men of reproductive potential who are not willing to use effective contraception for at least 3 months after radiation treatment
- People who are unlikely to follow the study procedures and attend required follow-up appointments
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Susanne Rogers, MD PhD, Kantonsspital Aarau, Radio-Onkologie-Zentrum Mittelland
Phone: +41 62 838 57 26
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Leptomeningeal disease
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.