Intraventricular CARv3-TEAM-E T Cells in Recurrent Glioblastoma.
Bryan D ChoiElizabeth R GerstnerMatthew J FrigaultMark B LeickChristopher W MountLeonora BalajSarah NikiforowBob S CarterWilliam T CurryKathleen GallagherMarcela V MausPublished in: The New England journal of medicine (2024)
In this first-in-human, investigator-initiated, open-label study, three participants with recurrent glioblastoma were treated with CARv3-TEAM-E T cells, which are chimeric antigen receptor (CAR) T cells engineered to target the epidermal growth factor receptor (EGFR) variant III tumor-specific antigen, as well as the wild-type EGFR protein, through secretion of a T-cell-engaging antibody molecule (TEAM). Treatment with CARv3-TEAM-E T cells did not result in adverse events greater than grade 3 or dose-limiting toxic effects. Radiographic tumor regression was dramatic and rapid, occurring within days after receipt of a single intraventricular infusion, but the responses were transient in two of the three participants. (Funded by Gateway for Cancer Research and others; INCIPIENT ClinicalTrials.gov number, NCT05660369.).
Keyphrases
- epidermal growth factor receptor
- tyrosine kinase
- palliative care
- advanced non small cell lung cancer
- quality improvement
- wild type
- open label
- small cell lung cancer
- endothelial cells
- low dose
- clinical trial
- radiation therapy
- small molecule
- cerebral ischemia
- protein protein
- amino acid
- induced pluripotent stem cells
- phase ii
- quantum dots
- placebo controlled