Repeated peripheral infusions of anti-EGFRvIII CAR T cells in combination with pembrolizumab show no efficacy in glioblastoma: a phase 1 trial.
Stephen J BagleyZev A BinderLamia LamraniEliana MarinariArati S DesaiMac Lean P NasrallahEileen MaloneySteven BremRobert A LustigGoldie KurtzMichelle Alonso-BasantaPierre-Emmanuel BonteChristel GoudotWilfrid RicherEliane PiaggioShawn KothariLea GuyonnetCoralie L GuerinJoshua J WaterfallSuyash MohanWei-Ting HwangOliver Y TangMeghan LogunMeghna BhattacharyyaKelly MarkowitzDevora DelmanAmy MarshallE John WherrySebastian AmigorenaGregory L BeattyJennifer L BrogdonElizabeth HexnerDenis MiglioriniCécile AlanioDonald M O'RourkePublished in: Nature cancer (2024)
We previously showed that chimeric antigen receptor (CAR) T-cell therapy targeting epidermal growth factor receptor variant III (EGFRvIII) produces upregulation of programmed death-ligand 1 (PD-L1) in the tumor microenvironment (TME). Here we conducted a phase 1 trial (NCT03726515) of CAR T-EGFRvIII cells administered concomitantly with the anti-PD1 (aPD1) monoclonal antibody pembrolizumab in patients with newly diagnosed, EGFRvIII + glioblastoma (GBM) (n = 7). The primary outcome was safety, and no dose-limiting toxicity was observed. Secondary outcomes included median progression-free survival (5.2 months; 90% confidence interval (CI), 2.9-6.0 months) and median overall survival (11.8 months; 90% CI, 9.2-14.2 months). In exploratory analyses, comparison of the TME in tumors harvested before versus after CAR + aPD1 administration demonstrated substantial evolution of the infiltrating myeloid and T cells, with more exhausted, regulatory, and interferon (IFN)-stimulated T cells at relapse. Our study suggests that the combination of CAR T cells and PD-1 inhibition in GBM is safe and biologically active but, given the lack of efficacy, also indicates a need to consider alternative strategies.
Keyphrases
- free survival
- epidermal growth factor receptor
- cell therapy
- advanced non small cell lung cancer
- monoclonal antibody
- dendritic cells
- newly diagnosed
- tyrosine kinase
- induced apoptosis
- stem cells
- oxidative stress
- cell proliferation
- type diabetes
- mesenchymal stem cells
- acute myeloid leukemia
- transcription factor
- metabolic syndrome
- cancer therapy
- weight loss
- endoplasmic reticulum stress
- cell death