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- W4383068800 endingPage "1770" @default.
- W4383068800 startingPage "1770" @default.
- W4383068800 abstract "Glioblastoma (GBM) is a highly aggressive primary brain tumor that is largely refractory to treatment and, therefore, invariably relapses. GBM patients have a median overall survival of 15 months and, given this devastating prognosis, there is a high need for therapy improvement. One of the therapeutic approaches currently tested in GBM is chimeric antigen receptor (CAR)-T cell therapy. CAR-T cells are genetically altered T cells that are redirected to eliminate tumor cells in a highly specific manner. There are several challenges to CAR-T cell therapy in solid tumors such as GBM, including restricted trafficking and penetration of tumor tissue, a highly immunosuppressive tumor microenvironment (TME), as well as heterogeneous antigen expression and antigen loss. In addition, CAR-T cells have limitations concerning safety, toxicity, and the manufacturing process. To date, CAR-T cells directed against several target antigens in GBM including interleukin-13 receptor alpha 2 (IL-13Rα2), epidermal growth factor receptor variant III (EGFRvIII), human epidermal growth factor receptor 2 (HER2), and ephrin type-A receptor 2 (EphA2) have been tested in preclinical and clinical studies. These studies demonstrated that CAR-T cell therapy is a feasible option in GBM with at least transient responses and acceptable adverse effects. Further improvements in CAR-T cells regarding their efficacy, flexibility, and safety could render them a promising therapy option in GBM." @default.
- W4383068800 created "2023-07-05" @default.
- W4383068800 creator A5017579441 @default.
- W4383068800 creator A5022493582 @default.
- W4383068800 creator A5064202628 @default.
- W4383068800 date "2023-07-03" @default.
- W4383068800 modified "2023-10-14" @default.
- W4383068800 title "Chimeric Antigen Receptor T Cells in Glioblastoma—Current Concepts and Promising Future" @default.
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