Actively Recruiting
Corticodependent or Corticoresistant Brain Radionecrosis After Radiotherapy for Brain Metastases
Led by Institut Cancerologie de l'Ouest · Updated on 2025-08-17
84
Participants Needed
10
Research Sites
274 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Brain metastases (BM) afflict a significant portion of cancer patients, ranging from 10% to 50%, leading to debilitating symptoms and diminished quality of life, thereby impacting overall survival. Treatment options typically include surgery, stereotactic radiosurgery (SRS), and whole brain radiotherapy (WBRT). SRS has emerged as the preferred focal treatment due to its efficacy, delivering ablative doses with notable overall survival benefits, especially for single BM or postoperative cases, while being less invasive than neurosurgery and capable of addressing inoperable sites and multiple lesions. Contrastingly, WBRT is now reserved for select cases with multiple BMs ineligible for SRS, owing to its lower rate of neurocognitive toxicities and high local control rates at one year. Despite its advantages, SRS can engender late side effects, with cerebral radio necrosis (RN) being the most common, occurring in approximately 10% of patients treated. The exact pathophysiology of RN remains unclear but is thought to involve vascular injury, immune-mediated mechanisms, and direct neuronal effects, culminating in radiological changes or symptomatic manifestations necessitating treatment. Corticosteroids are the mainstay therapy, albeit with associated side effects and instances of cortico-resistance or cortico-dependence. Bevacizumab, an anti-VEGF agent, has shown promise in small studies but awaits validation in larger trials. Consequently, a randomized phase III trial seeks to evaluate the efficacy of adding bevacizumab to standard corticosteroid therapy in patients with symptomatic RN. The trial aims to determine if this combination therapy yields superior symptomatic improvement compared to corticosteroids alone. RN will be diagnosed using multimodal imaging, and the primary objective is to assess the efficacy of bevacizumab in reducing corticosteroid usage and neurological symptoms associated with RN at three months. Secondary endpoints include toxicities, quality of life, imaging changes, and response duration. Additionally, an ancillary study will explore correlations between initial imaging parameters and treatment response, as well as changes in biological parameters with bevacizumab therapy.
CONDITIONS
Official Title
Corticodependent or Corticoresistant Brain Radionecrosis After Radiotherapy for Brain Metastases
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of radionecrosis based on symptoms and radiological findings after radiotherapy
- MRI evidence of radionecrosis combined with specific nuclear medicine imaging
- Persistent or worsening symptoms despite corticosteroids at a dose of at least 1 mg/kg/day
- Corticoresistant: symptoms despite at least 2 weeks of corticosteroids at 1 mg/kg/day
- Corticodependent: symptoms worsen when reducing corticosteroids below 0.5 mg/kg/day
- Last brain irradiation at least 3 months prior
- Age 18 years or older
- ECOG performance status score of 3 or less
- Life expectancy of at least 3 months with DS-GPA score 0.5 or greater
- No prior bevacizumab treatment for radionecrosis
- Adequate bone marrow, coagulation, renal, and liver function
- Women of childbearing potential must use effective contraception during and 6 months after treatment
- Signed informed consent
- Affiliated with a social security scheme
You will not qualify if you...
- Active bleeding or high risk of bleeding conditions including CNS hemorrhage and gastrointestinal complications within 28 days
- Grade 4 venous thromboembolism or peripheral arterial thrombus
- Very high intracranial pressure requiring emergency surgery
- Major surgery or significant trauma within 28 days; minor surgery within 3 days before treatment
- Significant cardiovascular disease including uncontrolled hypertension, recent myocardial infarction, arrhythmias, unstable angina, or heart failure within 6 months
- History of hypertensive crisis or encephalopathy
- Planned head, neck, thoracic, or abdominal radiotherapy during study treatment
- Prior bevacizumab treatment within 3 months before randomization
- Progressive brain metastases
- Severe allergic reactions to bevacizumab
- Known hypersensitivity to bevacizumab or its components
- Contraindication to bevacizumab treatment
- Pregnant or nursing women
- Mental impairment affecting consent or study compliance
- Legal restrictions on freedom or guardianship
- New brain metastasis detected during inclusion imaging
- Prior posterior reversible encephalopathy syndrome with bevacizumab
- Hypersensitivity to Chinese Hamster Ovary cell products or similar antibodies
AI-Screening
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Trial Site Locations
Total: 10 locations
1
CHRU de Brest
Brest, France, 29609
Actively Recruiting
2
Centre Francois Baclesse
Caen, France, 14000
Actively Recruiting
3
Centre D'Oncologie Et de Radiotherapie 37
Chambray-lès-Tours, France, 37170
Actively Recruiting
4
Centre Georges François Leclerc
Dijon, France, 21079
Not Yet Recruiting
5
Centre Guillaume le Conquérant
Le Havre, France, 76600
Actively Recruiting
6
Centre Léon Bérard
Lyon, France, 69373
Actively Recruiting
7
Centre Eugène marquis
Rennes, France, 35042
Actively Recruiting
8
Institut de Cancérologie de l'Ouest
Saint-Herblain, France, 44805
Actively Recruiting
9
Centre Paul Strauss
Strasbourg, France, 67000
Actively Recruiting
10
Centre Saint Yves
Vannes, France, 56000
Actively Recruiting
Research Team
L
Luc Ollivier, MD
CONTACT
M
Marine Tigreat
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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