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

27 Participants
are divided into 1 treatment group

Locations

1
City of Hope Medical Center91010, DuarteCalifornia, United States

Sponsors and collaborators

City of Hope Medical Center

Lead sponsor

National Cancer Institute (NCI)

Collaborator