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Safety and antitumor activity of GD2-Specific 4SCAR-T cells in patients with glioblastoma

Zhuohao Liu, Jiayi Zhou, Xinzhi Yang, Yuchen Liu, Chang Zou, Wen Lv, Cheng Chen, Kenneth K.Y. Cheng, Tao Chen, Lung‐Ji Chang, Dinglan Wu, Jie Mao

2023Molecular Cancer124 citationsDOIOpen Access PDF

Abstract

BACKGROUND: This study aimed to validate whether infusion of GD2-specific fourth-generation safety-designed chimeric antigen receptor (4SCAR)-T cells is safe and whether CAR-T cells exert anti-glioblastoma (GBM) activity. METHODS: A total of eight patients with GD2-positive GBM were enrolled and infused with autologous GD2-specific 4SCAR-T cells, either through intravenous administration alone or intravenous combined with intracavitary administration. RESULTS: 4SCAR-T cells expanded for 1-3 weeks and persisted at a low frequency in peripheral blood. Of the eight evaluable patients, four showed a partial response for 3 to 24 months, three had progressive disease for 6 to 23 months, and one had stable disease for 4 months after infusion. For the entire cohort, the median overall survival was 10 months from the infusion. GD2 antigen loss and infiltrated T cells were observed in the tumor resected after infusion. CONCLUSION: Both single and combined infusions of GD2-specific 4SCAR-T cells in targeting GBM were safe and well tolerated, with no severe adverse events. In addition, GD2-specific 4SCAR-T cells partially mediate antigen loss and activate immune responses in the tumor microenvironment. Validation of our findings in a larger prospective trial is warranted. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03170141 . Registered 30 May 2017.

Topics & Concepts

Chimeric antigen receptorMedicineAntigenAdverse effectProspective cohort studyImmune systemImmunotherapyInternal medicineImmunologyPharmacologyCAR-T cell therapy researchGlioma Diagnosis and TreatmentCancer Immunotherapy and Biomarkers
Safety and antitumor activity of GD2-Specific 4SCAR-T cells in patients with glioblastoma | Litcius