RecruitingPhase 1Phase 2NCT02861898

Super-selective Intra-arterial Repeated Infusion of Cetuximab for the Treatment of Newly Diagnosed Glioblastoma

Phase I/II Trial of Super-selective Intra-arterial Repeated Infusion of Cetuximab for the Treatment of Newly Diagnosed Glioblastoma


Sponsor

Northwell Health

Enrollment

33 participants

Start Date

Jun 1, 2016

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a way to deliver the targeted therapy drug cetuximab directly into the arteries feeding a brain tumor called glioblastoma — the most aggressive type of primary brain cancer — by injecting it through a catheter placed in the brain's blood vessels rather than through a standard IV line. **You may be eligible if...** - You are 18 or older - You have been newly diagnosed with glioblastoma confirmed by biopsy - Lab testing shows your tumor overexpresses a protein called EGFR, which cetuximab targets - You have at least one confirmed tumor site visible on brain imaging - You are in reasonably good health and able to function independently - Your expected survival is at least 3 months - You have not had chemotherapy in the past 2 weeks or radiation in the past 8 weeks **You may NOT be eligible if...** - Your tumor does not overexpress the EGFR protein - You have serious blood vessel problems that make the arterial procedure unsafe - You have had prior brain tumor treatment with overlapping radiation fields - You have severe kidney or liver disease Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGIntra-arterial Cetuximab
DRUGIntra-arterial Mannitol

Locations(1)

Lenox Hill Brain Tumor Center

New York, New York, United States

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NCT02861898


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