OncoMatch/Clinical Trials/NCT02800486
Super Selective Intra-arterial Repeated Infusion of Cetuximab (Erbitux) With Reirradiation for Treatment of Relapsed/Refractory GBM, AA, and AOA
Is NCT02800486 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Intra-arterial Cetuximab and Intra-arterial Mannitol for glioblastoma.
Treatment: Intra-arterial Cetuximab · Intra-arterial Mannitol — Primary brain tumors are typically treated by surgery, radiation therapy and chemotherapy, either individually or in combination. Present therapies are inadequate, as evidenced by the low 5-year survival rate for brain cancer patients, with median survival at approximately 12 months. Glioma is the most common form of primary brain cancer, afflicting approximately 7,000 patients in the United States each year. These highly malignant cancers remain a significant unmet clinical need in oncology. GBM often has a high expression of EFGR (Epidermal Growth Factor Receptor), which is associated with poor prognosis. Several methods of inhibiting this receptor have been tested, including monoclonal antibodies, vaccines, and tyrosine kinase inhibitors. The investigators hypothesize that in patients with recurring GBM, intracranial superselective intra-arterial infusion of Cetuximab (CTX), at a dose of 250mg/m2 in conjunction with hypofractionated radiation, will be safe and efficacious and prevent tumor progression in patients with recurrent, residual GBM.
Check if I qualifyExtracted eligibility criteria
Cancer type
Glioblastoma
Biomarker criteria
Required: EGFR overexpression
Prior therapy
Must have received: Stupp protocol
Patients who have not failed standard Stupp protocol
Cannot have received: chemotherapy
No chemotherapy for two weeks prior to treatment under this research protocol
Cannot have received: external beam radiation
no external beam radiation for eight weeks prior to treatment under this research protocol
Cannot have received: chemo/radiation therapy
Patients who completed chemo/RT less than 6 months prior to enrollment
Lab requirements
Blood counts
WBC ≥3000/mm3, absolute neutrophils ≥1500/mm3 and platelets ≥100,000/ mm3. Patients who are on Coumadin must have a platelet count of ≥150,000/ mm3
Kidney function
creatinine <1.5X IUNL
Liver function
bilirubin <1.5X the institutional upper limit of normal (IUNL); AST or ALT <2.5X IUNL
Patients must have adequate hematologic reserve with WBC≥3000/mm3, absolute neutrophils ≥1500/mm3 and platelets ≥100,000/ mm3. Patients who are on Coumadin must have a platelet count of ≥150,000/ mm3. Pre-enrollment chemistry parameters must show: bilirubin<1.5X the institutional upper limit of normal (IUNL); AST or ALT<2.5X IUNL and creatinine<1.5X IUNL. Pre-enrollment coagulation parameters (PT and PTT) must be ≤1.5X the IUNL
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Lenox Hill Brain Tumor Center · New York, New York
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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