Haaglanden Medisch Centrum
Leidschendam, South Holland, 2262 BA, Netherlands
Location status: Recruiting
NCT Number: NCT05346367
Randomized phase II trial. The study aims to investigate a different and potentially safer radio therapeutic treatment method for brain metastases. The current standard of stereotactic radiotherapy (SRT) in one or three fractions is compared to fractionated stereotactic radiotherapy (fSRT) in five fractions.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Leidschendam, South Holland, 2262 BA, Netherlands
Location status: Recruiting
Randomized phase II trial. Stereotactic radiotherapy is one of the most frequently chosen treatment options for brain metastases. There are an increasing number of long term survivors. Brain necrosis (e.g. radio necrosis) is the most important long term side effect of the treatment, occurring in up to 40% of patients, dependent on the size of the metastasis and delivered radiotherapy dose. Retrospective studies have shown that the incidence of radio necrosis, as well as local tumor recurrence, can be decreased with a risk difference of around 20% by administrating fractionated stereotactic radiotherapy (fSRT, e.g. five fractions) over single fraction stereotactic radiotherapy, especially in large brain metastases. In this trial, one group is treated with SRT in one or three fractions. The other group is treated with fSRT in five fractions. Survival, toxicity and patient reported quality of life are monitored.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
SRT
fSRT
Time frame: 2 years after treatment
Incidence of either radio necrosis or local failure according to Response Assessment in Neuro-Oncology Brain Metastases (RANO-BM).
Time frame: 2 years after treatment
median survival with Kaplan Meyer analysis
Time frame: 2 years after treatment
incidence of RN or LF within 2 years after SRT
Time frame: 2 years after treatment
incidence of salvage treatment within 2 years after SRT
Time frame: 2 years after treatment
incidence of distant brain recurrences within 2 years after SRT
Time frame: baseline - 2 years after treatment
Dose dexamethasone in mg per day
Time frame: baseline - 2 years after treatment
Anti-epileptic drug use in mg per day
Time frame: baseline - 2 years after treatment
incidence of Grade 2 or more toxicity according to CTCAE version 5.0 within 2 years after SRT
Contact information is provided by the study sponsor or research team.
Jaap D Zindler, MD, PhD
CONTACT
Mirjam Mast, PhD
CONTACT
Haaglanden Medical Centre
Other
Acronym: SAFESTEREO
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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