RecruitingPhase 3NCT06888817

Bevacizumab Versus Corticosteroids as First-line Treatment in Patients With Symptomatic Cerebral Radiation Necrosis After Radiation for High-grade Glioma or Brain Metastases

Bevacizumab for the Treatment of Cerebral RAdiation Induced NecrosiS (BRAINS) Study: a Multicenter, Open-label, Randomized Clinical Trial to Assess the Clinical Efficacy and Cost-effectiveness of Bevacizumab Versus Corticosteroids as First-line Treatment in Patients With Symptomatic Cerebral Radiation Necrosis After Radiation for High-grade Glioma or Brain Metastases


Sponsor

The Netherlands Cancer Institute

Enrollment

408 participants

Start Date

Jun 19, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Cerebral radiation necrosis (CRN) is a severe complication of high-dose radiation for brain metastases (BM) or glioma, which can potentially cause significant neurologic symptoms leading to serious morbidity and impaired quality of life (QoL). The first-line therapy for symptomatic CRN (sCRN) is corticosteroids, primarily dexamethasone, which often leads to complications, refractory symptoms, and interference with anti-cancer treatment. Since 2017, bevacizumab, an antibody against Vascular Endothelial Growth Factor (VEGF), has been used in a second-line treatment setting for refractory sCRN. A small randomized clinical trial (RCT) has shown that bevacizumab significantly diminishes cerebral edema on MRI and decreases clinical symptoms of sCRN in irradiated glioma patients. Several non-randomized clinical studies demonstrated a beneficial radiological and clinical effect of bevacizumab in patients with sCRN after irradiation for BM. The optimal first-line treatment for sCRN is currently unknown. Effective and safe first-line treatment of sCRN will optimize the patient's well-being and health-related QoL. Furthermore, minimizing corticosteroid use will benefit the clinical treatment options and outcomes of concomitant or future anti-cancer treatment. This phase III multicenter, open-label, randomized clinical trial compares the clinical efficacy of first-line bevacizumab versus standard-of-care dexamethasone for sCRN in patients with high-grade glioma (HGG) or BM.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study compares two treatments for radiation necrosis — damage to brain tissue that can occur months after radiation therapy for brain tumors or cancer spread to the brain. It compares bevacizumab (a drug that targets blood vessel growth) with corticosteroids (anti-inflammatory steroids) to see which works better and is safer. **You may be eligible if...** - You are 18 or older - You have had radiation therapy for a high-grade brain tumor or brain metastases - You developed radiation necrosis at least 3 months after completing radiation - Your symptoms have affected daily functioning (documented by a clinical scale) - A tumor board has confirmed your diagnosis is radiation necrosis, not tumor recurrence **You may NOT be eligible if...** - Your brain shows signs of tumor progression mixed with the necrosis - You have already received treatment for this radiation necrosis episode - You have certain conditions that make bevacizumab unsafe (like recent surgery or uncontrolled blood pressure) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGBevacizumab

Intravenous bevacizumab at a 600 mg flat dose every three weeks for four courses over 12 weeks

DRUGDexamethasone

Daily oral dexamethasone followed by a protocol-based tapering dose over 12 weeks


Locations(5)

Netherlands Cancer Institute - Antoni van Leeuwenhoek

Amsterdam, Netherlands

Amsterdam University Medical Centers, location VUmc and AMC

Amsterdam, Netherlands

Leiden University Medical Center

Leiden, Netherlands

Haaglanden Medical Center

The Hague, Netherlands

University Medical Center Utrecht

Utrecht, Netherlands

View Full Details on ClinicalTrials.gov

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NCT06888817


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