Actively Recruiting
Super-selective Intra-arterial Repeated Infusion of Cetuximab for the Treatment of Newly Diagnosed Glioblastoma
Led by Northwell Health · Updated on 2025-04-09
33
Participants Needed
1
Research Sites
600 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Primary brain cancer kills up to 10,000 Americans a year. These 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 EFGR (Epidermal Growth Factor Receptor) which is blocked by Cetuximab (CTX). The investigators have recently completed a separate Phase I clinical trial using superselective intra-arterial cerebral infusion (SIACI) of CTX after blood brain barrier disruption (BBBD) for recurrent GBM (Chakraborty et al, in revision, Journal of Neurooncology). The investigators found that intra-arterial infusion of CTX is well tolerated with few adverse effects. The investigators hypothesize that in patients with newly diagnosed GBM, repeated SIACI of this drug after BBBD will be safe and efficacious for our patients when combined with standard chemoradiation (STUPP protocol). This trial will be a non-randomized open label Phase I/II clinical trial. In addition to standard chemotherapy and radiation therapy (STUPP protocol) the patient will be given CTX intra-arterially after BBBD for a total of three doses at approximately post surgery days 30, 120 and 210.
CONDITIONS
Official Title
Super-selective Intra-arterial Repeated Infusion of Cetuximab for the Treatment of Newly Diagnosed Glioblastoma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female patients 18 years of age or older
- Documented histologic diagnosis of newly diagnosed glioblastoma multiforme (GBM)
- Pathology confirmed histologic EGFR overexpression
- At least one confirmed and evaluable tumor site verified by biopsy
- Karnofsky performance status 70% or higher (or equivalent ECOG level 0-2)
- Expected survival of at least three months
- No chemotherapy within two weeks before starting this study treatment
- No external beam radiation within eight weeks before starting this study treatment
- Adequate blood counts: WBC at least 3000/mm3, absolute neutrophils at least 1500/mm3, platelets at least 100,000/mm3 (or at least 150,000/mm3 if on Coumadin)
- Pre-enrollment chemistry tests showing bilirubin less than 1.5 times the upper limit of normal, AST or ALT less than 2.5 times the upper limit of normal, and creatinine less than 1.5 times the upper limit of normal
- Pre-enrollment coagulation tests (PT and PTT) at or below 1.5 times the upper limit of normal
- Agreement to use effective contraception during and for three months after treatment
- Ability to understand and provide written informed consent
You will not qualify if you...
- Women who are pregnant or breastfeeding
- Patients with significant medical or psychiatric conditions increasing risk or interfering with treatment or monitoring
- Patients with radiological evidence of leptomeningeal disease
- History of allergic reaction to Cetuximab (CTX)
- Patients who have already started or completed chemotherapy or radiation therapy for this condition
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Lenox Hill Brain Tumor Center
New York, New York, United States, 10075
Actively Recruiting
Research Team
J
John Boockvar, MD
CONTACT
T
Tamika Wong, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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