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Recruiting Phase 3

Corticodependent or Corticoresistant Brain Radionecrosis After Radiotherapy for Brain Metastases

NCT06471465 · tracked via the Priya Life Science France tracker
Phase
Phase 3
Started
2025-04-29
Last updated
2025-08-17

Condition(s) studied

Radionecrosis of BrainBrain Metastases

Investigational drug(s) / intervention(s)

Bevacizumab →PlaceboPrednisolone →

Bevacizumab: Drug: bevacizumab IV

Placebo: Drug: placebo IV

Prednisolone: Drug: corticosteroids IV

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient with a diagnosis of radionecrosis based on a clinical onset of symptoms and radiological findings of RN following radiotherapy, with or without pathological confirmation: MRI evidence to support the diagnosis of RN (transient increase in irradiated lesion volume -FLAIR hypersignal and/or enhanced portion- without rCBV increase) COMBINED with nuclear medicine imaging: biphasic 18FDG-PET-TDM/MRI according to Horky or 18F-FDOPA with stage 0-1 according to Lizarraga; * Symptoms are persistent or worsening despite administration of corticosteroids: at least 1 mg/kg/d of prednisolone or equivalent: Corticoresistant: neurological symptoms despite administration of at least 2 weeks of 1 mg/kg/d prednisolone or equivalent; Corticodependant: worsening of neurological signs or symptoms after an initial improvement when weaning off steroids at a dose \< 0.5 mg/kg/d prednisolone or equivalent; * Patients must have received the last cranial irradiation with photons or proton therapy for brain metastases ≥ 3 months with one or more sequences; * Age≥18-year-old; * ECOG performance status score ≤ 3 * Life expectancy of at least 3 months assessed by graded prognostic score (DS-GPA) score 0.5 or greater; * Patient who has never received Bevacizumab for the indication of radionecrosis. * Adequate organ function: Bone marrow function * Absolute Neutrophil Count (ANC) ≥ 1,500/mm3 Platelet Count ≥ 100,000/mm3, Haemoglobin ≥ 10 g/dL (allowing transfusion or other intervention to achieve this minimum haemoglobin) Coagulation * International normalized ratio (INR) or prothrombin time \< 1.5 × ULN Renal function * No proteinuria with urine dipstick for proteinuria \> 2+ * Serum creatinine ≤1.5 x ULN or creatinine clearance ≥50 mL/min (measured or calculated using the CDK-EPI formula) Hepatic Function * Total bilirubin ≤1.5 x the upper limit of normal (ULN) * Alanine transaminase (ALT) and aspartate aminotransferase (AST) ≤3 x ULN * Women of childbearing potential must use effective contraceptive measures during the treatment and for 6 months following its cessation; * Signed informed consent; * Patient affiliated to a social security scheme. Exclusion Criteria: * Evidence of active bleeding or a pathological condition at high risk of bleeding: CNS hemorrhage, bleeding diathesis or coagulopathy, hemoptysis (\>2.5ml of bright red blood per episode), evidence of history of bowel obstruction, abdominal fistula, or gastrointestinal tract perforation or gastro intestinal abscess occurring less than 28 days prior study entry; * Grade 4 venous thromboelism and peripheral arterial thrombus * Evidence of very high intracranial pressure that suggests brain hernia and needs emergency surgery; * Major surgical procedure or significant traumatic injury less than 28 days prior study entry; minor surgery within 3 days prior to initiation of study treatment; * Clinically significant cardiovascular disease such as uncontrolled arterial hypertension (BP ≥160 mm Hg or diastolic BP ≥100 mm Hg despite maximal medical therapy), cerebrovascular event, myocardial infarction, cardiac arrhythmias, unstable angina, or congestive heart failure within the last 6 months; * History of hypertensive crisis or hypertensive encephalopathy * Patients scheduled to undergo head and neck, thoracic, or abdominal radiotherapy during the study treatment * Prior bevacizumab ≤ 3 months before randomization; * Progressive brain metastases; * History of severe allergic anaphylactic reactions to bevacizumab * Patients with a known hypersensitivity to the active substance or to any of the excipients of bevacizumab are not eligible for participation; * Patients with a contraindication to the treatment with bevacizumab according to the European SmPC * Patient pregnant and/or nursing; * Mental impairment (psychiatric illness/social situations) that may compromise the ability of the patient to give informed consent and comply with the requirements of the study; * Patient who has forfeited his/her freedom by administrative or legal award or who is under guardianship; * New cerebral metastasis detected during the inclusion imaging evaluation; * Prior diagnosis of Posterior Reversible Encephalopathy Syndrome (PRES) with bevacizumab; * Hypersensitivity known to Chinese Hamster Ovary (CHO) cell products or other recombinant human or humanised antibodies.

Primary outcome measure(s)

  • Efficacy at 90 days on decrease in corticosteroids — 90 days after start of treatment
    To investigate whether the addition of bevacizumab to standard corticosteroid therapy, compared to corticosteroid therapy plus placebo, results in greater efficacy at 3 months (90 days) on decrease in corticosteroids with radionecrosis (RN) after radiotherapy for brain. metastases. Will be assessed corticosteroids dose at Cycle 1 Day 1 and at 3 months (90 days after Cycle 1 Day 1, End of treatment visit)

Trial sites (10)

FacilityCityRegionStatus
CHRU de Brest Brest France Recruiting
Centre Francois Baclesse Caen France Recruiting
Centre D'Oncologie Et de Radiotherapie 37 Chambray-lès-Tours France Recruiting
Centre Georges François Leclerc Dijon France Not Yet Recruiting
Centre Guillaume le Conquérant Le Havre France Recruiting
Centre Léon Bérard Lyon France Recruiting
Centre Eugène marquis Rennes France Recruiting
Institut de Cancérologie de l'Ouest Saint-Herblain France Recruiting
Centre Paul Strauss Strasbourg France Recruiting
Centre Saint Yves Vannes France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06471465 on ClinicalTrials.gov ↗ ← All trials in France