About this trial
The purpose of this study is to evaluate the local control rate on the target lesion at 6, 12, and 24 months after treatment with neoadjuvant stereotactic radiotherapy (SRS NEO group) compared to standard care, adjuvant stereotactic radiotherapy (POST OP SRS group).
Eligibility criteria
Qualifiers
Patients aged 18 years and older;
Patients with 1 to 12 brain metastases on preoperative MRI, at least one of which (contrast enhancement of at least 1 cm) is accessible for the most complete possible resection (target lesion);
Patients with a Karnofsky performance score of ≥ 70;
Patients able to perform neurocognitive tests without assistance;
Disqualifiers
Patient who has already been treated with surgery, radiosurgery, and/or radiotherapy for the target brain metastasis;
Medical contraindication to MRI;
Patient with an estimated life expectancy of ≤ 3 months;
Patients participating in another clinical trial, or who are in the exclusion period of another clinical trial;
Trial design
Treatments tested in this trial
- stereotactic radiotherapy
- Excision surgery
Treatment groups
Sponsors and collaborators
GCS Ramsay Santé pour l'Enseignement et la Recherche
Lead sponsor
Euraxi Pharma
Collaborator