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

Glioblastoma Clinical Trial

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02861898
• Other study ID #: HS16-0257
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: June 2016
• Est. completion date: December 2026

Study information

• Verified date: January 2024
• Source: Northwell Health
• Contact: John Boockvar, MD
• Phone: 212-434-4836
• Email: jboockvar[@]northwell.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 33
• Est. completion date: December 2026
• Est. primary completion date: December 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female patients of =18 years of age.
• Patients with a documented histologic diagnosis of newly diagnosed glioblastoma multiforme (GBM)
• Patients with pathology confirmed histologic EGFR overexpression
• Patients must have at least one confirmed and evaluable tumor site.* *A confirmed tumor site is one in which is biopsy-proven. NOTE: Radiographic procedures (e.g., Gd-enhanced MRI or CT scans) documenting existing lesions must have been performed within two weeks of treatment on this research study.
• Patients must have a Karnofsky performance status =70% (or the equivalent ECOG level of 0-2) and an expected survival of = three months.
• No chemotherapy for two weeks prior to treatment under this research protocol and no external beam radiation for eight weeks prior to treatment under this research protocol.
• 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.
• Patients must agree to use a medically effective method of contraception during and for a period of three months after the treatment period. A pregnancy test will be performed on each premenopausal female of childbearing potential immediately prior to entry into the research study.
• Patients must be able to understand and give written informed consent. Informed consent must be obtained at the time of patient screening.

Exclusion Criteria:

• Women who are pregnant or lactating.
• Women of childbearing potential and fertile men will be informed as to the potential risk of conception while participating in this research trial and will be advised that they must use effective contraception during and for a period of three months after the treatment period.
• Patients with significant intercurrent medical or psychiatric conditions that would place them at increased risk or affect their ability to receive or comply with treatment or post-treatment clinical monitoring
• Patients with radiological evidence of leptomeningeal disease.
• Patients with history of allergic reaction to CTX
• Patients who initiated or completed chemo/RT

Related Conditions & MeSH terms

• Brain Cancer
• Brain Neoplasm
• Brain Neoplasm, Malignant
• Brain Neoplasms
• Brain Tumor
• EGFR Gene Overexpression
• GBM
• Glioblastoma
• Neoplasms

Intervention

Drug:
• Intra-arterial Cetuximab

• Intra-arterial Mannitol

Locations

Country	Name	City	State
United States	Lenox Hill Brain Tumor Center	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
Northwell Health

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression Free Survival (PFS)	The 6-month PFS will be estimated by calculating the proportion of patients who are alive at 6 months from treatment commencement and are progression-free.	6 months
Primary	Overall Survival (OS)	OS will be calculated as the time from treatment initiation to the date of death.	2 years
Secondary	Composite overall response rate (CORR) through the Response Assessment in Neuro-Oncology (RANO)	Subjects will be classified according to the RANO criteria, which is a composite of MRI changes, clinical response and changes in steroid use.	6 months
Secondary	Toxicities graded according to the NCI Common Toxicity Criteria (CTCAE) version 4.03	Toxicities will be tabulated and graded according to the NCI Common Toxicity Criteria (CTCAE) version 4.03	6 months