Actively Recruiting

Phase 1
Phase 2
Age: 18Years +
All Genders
NCT02861898

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Lenox Hill Brain Tumor Center

New York, New York, United States, 10075

Actively Recruiting

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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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