About this trial
This phase I trial tests the safety, side effects and best dose of TGFβR2KO/IL13Rα2 chimeric antigen receptor (CAR) T-cells given within the skull (intracranial) in treating patients with glioblastoma or IDH-mutant grade 3 or 4 astrocytoma that has come back after a period of improvement (recurrent) or that is growing, spreading, or getting worse (progressive). CAR T-cell therapy is a type of treatment in which a patient's T cells (a type of immune system cell) are changed in the laboratory so they will attack tumor cells. T cells are taken from a patient's blood. When the cells are taken from the patient's own blood, it is known as autologous. Then the gene for special receptors that bind to a certain proteins on the patient's tumor cells are added to the T cells in the laboratory. The special receptors are called CAR. Large numbers of the CAR T cells are grown in the laboratory and given to the patient by infusion for treatment of certain tumors. Giving TGFβR2KO/IL13Rα2 CAR T cells may be safe, tolerable, and/or effective in treating patients with recurrent or progressive glioblastoma or grade 3 or 4 IDH-mutant astrocytoma.
Eligibility criteria
Qualifiers
Documented informed consent of the participant and/or legally authorized representative
Note: For research participants who do not speak English, a short form consent may be used with a City of Hope (COH) certified interpreter/translator to proceed with screening and leukapheresis, while the request for a translated main consent is processed. However, the research participant is allowed to proceed with surgery/Rickham placement and CAR T cell infusion only after the translated main consent form is signed
Agreement to allow the use of archival tissue from diagnostic tumor biopsies. If unavailable, exceptions may be granted with study principal investigator (PI) approval
Age: ≥ 18 years
Disqualifiers
Owing to higher frequency of wound-related complications, participants who require active bevacizumab therapy at the time of enrollment are excluded
Participant has not yet recovered from toxicities of prior therapy
Uncontrolled seizure activity and/or clinically evident progressive encephalopathy
History of allergic reactions attributed to compounds of similar chemical or biologic composition to study agent
Trial design
Treatments tested in this trial
- Biospecimen Collection
- Chimeric Antigen Receptor T-Cell Therapy
- Echocardiography
- Fludeoxyglucose F-18
- Intracranial Catheter Placement
- Leukapheresis
- Magnetic Resonance Imaging
- Positron Emission Tomography
- Resection
Treatment groups
Sponsors and collaborators
City of Hope Medical Center
Lead sponsor
National Cancer Institute (NCI)
Collaborator