The Efficacy and Safety of Brain-targeting Immune Cells (EGFRvIII-CAR T Cells) in Treating Patients With Leptomeningeal Disease From Glioblastoma. Administering Patients EGFRvIII -CAR T Cells May Help to Recognize and Destroy Brain Tumor Cells in Patients

Glioblastoma Clinical Trial

— CARTREMENDOUS  

Official title:

A Phase 1 Study to Evaluate EGFRvIII -Targeted Chimeric Antigen Receptor (CAR) T Cells for Adult Patients With Leptomeningeal Glioblastoma

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05063682
• Other study ID #: 6678EGFRvIII
• Status: Active, not recruiting
• Phase: Phase 1
• Start date: May 15, 2020
• Est. completion date: October 2023

Study information

• Verified date: September 2021
• Source: Chembrain LTD
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This phase I trial investigates the efficacy and safety of brain-targeting epidermal growth factor receptor chimeric antigen receptor immune cells (EGFRvIII-CAR T cells) in treating patients with leptomeningeal disease from glioblastoma. T cells are part of the immune system and help the body fight malignant tumours. Immune cells can be genetically modified to destroy brain tumor cells in the laboratory. EGFRvIII -CAR T cells are brain tumor specific and can enter and express its genes in immune cells. Administering patients EGFRvIII -CAR T cells may help to recognize and destroy brain tumor cells in patients with leptomeningeal disease from glioblastoma.

Description:

PRIMARY OBJECTIVES: 1. Examine and describe the safety and feasibility of EGFRvIII-specific hinge-optimized CD3 ζ-stimulatory/41BB-co-stimulatory Chimeric Antigen Receptor autologous T-lymphocytes (EGFRvIII -CAR T cells) through intracerebroventricular (ICV) delivery as adjuvant therapy in participants with EGFRvIII+ leptomeningeal disease from glioblastoma. 2. Determine the activity of EGFRvIII -CAR T cells based on survival rate at 12 months for both arms. SECONDARY OBJECTIVES: 1. Describe persistence, expansion and phenotype of endogenous and EGFRvIII -CAR T cells in peripheral blood (PB), tumor cyst fluid (TCF) and cerebral spinal fluid (CSF) at applicable time points 2. Describe cytokine levels in PB, TCF, and CSF at applicable time points 3. Estimate the rate of disease response by Response Assessment in Neuro-Oncology Leptomeningeal Metastases (RANO LM) criteria 4. Estimate rate of progression free survival at 6 months. Estimate rate of overall survival (OS) at 12 months by study arm. 5. Estimate time to next treatment 6. Evaluate EGFRvIII -CAR T cell persistence in the tumor tissue and the location of the EGFRvIII -CAR T cells with respect to the infusion site. 7. Evaluate biomarkers and cytokine levels OUTLINE: Patients receive EGFRvIII -CAR T cells intracerebroventricular over 15 minutes on day 1. Patients may receive additional cycles based on the persistence of the cells. The patients are followed extensively according to the clinical pharmacology sampling plan; on days 1-30, months 2-12, and three times per year up to 10 years based on response

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 10
• Est. completion date: October 2023
• Est. primary completion date: October 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Participant has been treated for leptomeningeal metastases after intrathecal chemotherapy and/or radiation OR refuses to undergo additional radiation and/or intrathecal chemotherapy
• Participant must have a Karnofsky performance status (KPS) >= 60
• Participant must have a life expectancy of >= 2 months
• Women of child-bearing potential must have negative serum pregnancy test and agree to use a reliable form of birth control prior to study entry and for at least two months following study treatment. Male research participants must agree to use a reliable form of birth control and not donate sperm during the study and for at least two months following study treatment
• Participant has a histologically confirmed EGFRvII+ (epidermal growth factor receptor) tumor expression by immunohistochemistry (IHC) at the initial tumor presentation or recurrent disease (H-score >= 50)
• Participant or legal guardian must have the ability to understand and the willingness to sign a written informed consent

Exclusion Criteria:

• Research participant requires supplemental oxygen to keep saturation greater than 95%
• Research participant requires dialysis
• Research participant has uncontrolled seizure activity and/or clinically evident progressive encephalopathy
• Failure of research participant or legal guardian to understand the basic elements of the protocol and/or the risks/benefits of participating in the study.
• Participant is unwilling to stop treatment with chemotherapy or endocrine therapy and/or radiation one week prior and during the first 4 cycles of the study
• Participant has ventriculoperitoneal shunt
• Participant has a coagulopathy or bleeding disorder
• Participant is HIV+ (human immunodeficiency virus) or has acute CMV (cytomegalovirus) infection
• Participant has any uncontrolled illness, including ongoing or active infection; participant has known active hepatitis B or C infection; participants with any signs or symptoms of active infection, positive blood cultures or radiological evidence of infections
• Participant has an autoimmune disease that requires constant treatment
• Participant has another active malignancy
• Participant is unable to undergo a brain magnetic resonance imaging (MRI)
• Participant is pregnant or breast feeding

Related Conditions & MeSH terms

• Glioblastoma
• Glioblastoma Multiforme
• Glioma
• Glioma, Malignant

Intervention

Biological:
• EGFRvIII-specific hinge-optimized CD3 ?-stimulatory/41BB-co-stimulatory Chimeric Antigen Receptor autologous T-lymphocytes
ICV administration

Locations

Country	Name	City	State
Finland	Jyväskylä Central Hospital	Jyväskylä
Finland	University Of Oulu	Oulu
India	Apollo Hospital	New Delhi

Sponsors (4)

Lead Sponsor	Collaborator
Chembrain LTD	Apollo Hospital, New Delhi, India, Jyväskylä Central Hospital, University of Oulu

Countries where clinical trial is conducted

Finland,  India, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of adverse events	Common Terminology Criteria for Adverse Events (CTCAE) version 5.0	Up to 10 years
Primary	Overall survival		12 months
Secondary	CAR (chimeric antigen receptor) T cell levels detected in tumor cyst fluid (TCF), peripheral blood (PB), and cerebrospinal fluid (CSF)	Measured by absolute number per ul by flow	Up to 6 cycles (3 months), at the end of each cycle 1 (each cycle is 14 days)
Secondary	Endogenous T cell levels detected in tumor cyst fluid (TCF), peripheral blood (PB), and cerebrospinal fluid (CSF)	Measured by absolute number per ul by flow	Up to 6 cycles (3 months), at the end of each cycle 1 (each cycle is 14 days)
Secondary	Cell phenotype detected in tumor cyst fluid (TCF), peripheral blood (PB), and cerebrospinal fluid (CSF)	Measured by absolute number per ul by flow	Up to 6 cycles (3 months), at the end of each cycle 1 (each cycle is 14 days)
Secondary	Cytokine levels (Procartaplex panel) in PB, TCF and CSF		Up to 6 cycles (3 months), at the end of each cycle 1 (each cycle is 14 days)
Secondary	Disease response	Measured by Response Assessment in Neuro-Oncology Criteria (RANO LM).	Up to 10 years
Secondary	Time to progression	Progression defined by RANO LM criteria	Up to 10 years
Secondary	Overall survival		Up to 10 years
Secondary	CAR T and endogenous cells detected in tumor tissue	Detected in tumor tissue by immunohistochemistry (IHC)	Baseline and additional time points according to response (through study completion, up to 10 years by as needed basis)
Secondary	EGFRvII (epidermal growth factor receptor) antigen expression levels in tumor tissue.	Descriptive statistics will be provided	Baseline and additional time points according to response (through study completion, up to 10 years by as needed basis)