OncoMatch/Clinical Trials/NCT02847559
Optune Delivered Electric Field Therapy and Bevacizumab in Treating Patients With Recurrent or Progressive Grade 2 or 3 Meningioma
Is NCT02847559 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Bevacizumab and NovoTTF-200A Device for anaplastic (malignant) meningioma.
Treatment: Bevacizumab · NovoTTF-200A Device — The purpose of this research study is to determine the effects bevacizumab (the study drug) combined with Optune (the study device) tumor treatment field therapy has on meningiomas. Bevacizumab is considered investigational because the US Food and Drug Administration (FDA) has not approved its use for the treatment of meningiomas. The study drug is a medication that blocks the growth of new blood vessels. It is thought that the study drug may interfere with the growth of new blood vessels and therefore might stop tumor growth, and possibly shrink the tumor by keeping it from receiving nutrients and oxygen supplied by the blood vessels. Optune is also considered investigational because the US FDA has not approved its use for the treatment of meningiomas. Optune is a device that the patient will wear and use for at least 18 hours of each day. It delivers alternating electrical current to the patient's brain tumor and by doing so interrupts a process called mitosis. Mitosis needs to occur in order for cell division to occur and allows tumors to grow. By slowing this process, we hypothesize that meningioma growth may also be slowed.
Check if I qualifyExtracted eligibility criteria
Cancer type
Glioblastoma
Disease stage
Required: Stage GRADE II, GRADE III (WHO)
Grade: 23 (WHO)
WHO grade 2 or 3 (atypical or anaplastic)
Prior therapy
Must have received: surgical resection — if possible
Surgical resection, if possible
Must have received: definitive radiation therapy — for unresectable meningioma, or for recurrent meningioma after resection
Definitive radiation therapy for unresectable meningioma, or for recurrent meningioma after resection
Cannot have received: bevacizumab (bevacizumab)
Previous treatment with bevacizumab
Lab requirements
Blood counts
anc >= 1500/ul (with/without growth factor); hgb >= 9 g/dl (with/without transfusion); platelets >= 100,000/l
Kidney function
serum creatinine <= 1.5 x institutional uln
Liver function
ast and alt <= 2.5 x institutional uln; total bilirubin <= 1.5 x institutional uln
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- John Wayne Cancer Center at Providence St. John's Health Center · Santa Monica, California
- Miami Cancer Institute · Miami, Florida
- Piedmont Healthcare · Atlanta, Georgia
- Northwestern University · Chicago, Illinois
- Northwestern University- Lake Forest Hospital · Lake Forest, Illinois
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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