Glioblastoma, Glioma
Conditions
Brief summary
The purpose of this study is to evaluate the safety of the ExAblate Model 4000 Type 2 used as a tool to disrupt the BBB (blood brain barrier) in patients with high grade glioma undergoing standard of care therapy.
Detailed description
This is a prospective, multi-center, single-arm study to establish the safety and feasibility of BBB (blood brain barrier) disruption along the periphery of tumor resection cavity using the ExAblate Neuro Model 4000 Type 2 (220 kHz) system. For this study, patients will be eligible to enroll in the study prior to beginning the planned adjuvant TMZ chemotherapy phase of treatment. Of note, only patients who are deemed eligible for adjuvant TMZ will be eligible for enrollment.
Interventions
DEVICEFocused ultrasound (FUS)
FUS involves the application of acoustic energy at low frequencies from over 1000 individual transducers into distinct body targets.
Sponsors
InSightec
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
1. Patient is eligible for adjuvant temozolomide (TMZ) treatment based on the current standard of care. 2. Men or women age between 18 and 80 years, inclusive. 3. Able and willing to give informed consent. 4. Grade IV glioma (GBM) 5. Combined radiation/TMZ treatment is completed based on the prescribed standard of care regimen. 6. Karnofsky rating 70-100. 7. Able to communicate during the ExAblate BBBD (Blood Brain Barrier Disruption) procedure. 8. Able to attend all study visits (i.e., life expectancy of at least 3 months).
Exclusion criteria
1. Patients presenting with the following imaging characteristics: i. Evidence of acute intracranial hemorrhage. 2. The sonication pathway to the tumor involves: i. Extensive scalp sores. ii. Clips or other metallic implanted objects in the skull or the brain (brain implants) 3. The subject presents with symptoms and signs of increased intracranial pressure (e.g., headache, nausea, vomiting, lethargy, and papilledema). 4. Patients with cerebellar or brainstem tumors. 5. Patients with positive HIV status. 6. Significant depression not adequately controlled with medication and at potential risk of suicide. 7. Patient receiving bevacizumab (Avastin) therapy. 8. Patients receiving treatment with corticosteroid doses greater than dexamethasone 24 mg daily (or equivalent). 9. Patients undergoing other concurrent therapies such as chemotherapy wafers, immunotoxins delivered by convection-enhanced delivery, regionally administered gene and viral therapies, immunotherapies, focal irradiation with brachytherapy, stereotactic radiosurgery, laser interstitial thermotherapy, and tumor treatment fields therapy. 10. Cardiac disease or unstable hemodynamics including: i. Documented myocardial infarction within six months of enrollment. ii. Unstable angina on medication. iii. Congestive heart failure. iv. Left ventricular ejection fraction \<50%. v. History of a hemodynamically unstable cardiac arrhythmia. vi. Cardiac pacemaker. 11. Severe hypertension (diastolic BP \> 100 on medication). 12. Anti-coagulant therapy, or medications known to increase risk of hemorrhage within washout period prior to treatment. 13. History of a bleeding disorder, coagulopathy or with a history of spontaneous tumor hemorrhage. 14. Cerebral or systemic vasculopathy, including intracranial thrombosis, vascular malformation, cerebral aneurysm or vasculitis. 15. History of drug or alcohol use disorder. 16. Active seizure disorder or epilepsy (seizures despite medical treatment). 17. Known sensitivity to gadolinium-based contrast agents. 18. Known sensitivity to DEFINITY® ultrasound contrast agent or perflutren. 19. Contraindications to MRI such as non-MRI-compatible implanted devices. 20. Large subjects not fitting comfortably into the MRI scanner. 21. Difficulty lying supine and still for up to 4 hours in the MRI unit or claustrophobia. 22. Positive pregnancy test (women of childbearing potential). 23. Severely impaired renal function or on dialysis. 24. Cardiac shunt. 25. Subjects with evidence of cranial or systemic infection. 26. Subjects with significant liver dysfunction, e.g., history of cirrhosis or active hepatitis.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Device and procedure related adverse events | Throughout the study, approximately 12 months. | The number and severity of device and BBB disruption procedure related adverse events will be evaluated and classified according to the CTCAE |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Feasibility of repeated BBB disruption will be evaluated through assessment of post-procedure contrast-enhanced magnetic resonance (MR) imaging | At the time of each ExAblate MRgFUS procedure | The repeatability of BBB disruption will be evaluated at each of the 6 procedures and will be evaluated through assessment of post-procedure contrast-enhanced MR imaging. |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORGraeme Woodworth, MD
University of Maryland
Outcome results
None listed