Highlights in IO: next-generation CAR-T therapy for glioblastoma

Over the past few years, outcomes and findings from several phase 1 clinical trials evaluating chimeric antigen receptor (CAR)-T cell therapies for glioblastoma (GBM) have been reported. For CAR-T cell therapy to succeed in GBM, several challenges must be overcome, including the immunosuppressive microenvironment (immunosuppressive cells, hypoxia, and metabolic constraints), antigen heterogeneity, and the anatomically isolated environment. To address these challenges, next-generation CAR-T cells-those engineered with additional functionalities-have been developed, and phase 1 clinical trials evaluating these next-generation CAR-T therapies for GBM have now been initiated. The development of CAR-T therapy for GBM has entered a new chapter. To date, the antitumor efficacy of CAR-T therapies still needs to be improved, and the high frequency of neurotoxicity remains a major issue that needs to be addressed; however, there is a growing anticipation that next-generation CAR-T therapies may provide clinical benefit to patients.

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Publication Details

Journal
Journal for ImmunoTherapy of Cancer
Published
2026-04-01
DOI
https://doi.org/10.1136/jitc-2025-014670
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00

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article

Highlights in IO: next-generation CAR-T therapy for glioblastoma

Hideho Okada, Junya Yamaguchi
Journal for ImmunoTherapy of Cancer
CAR-T cell therapy research
article

Highlights in IO: next-generation CAR-T therapy for glioblastoma

Hideho Okada, Junya Yamaguchi
article en

Abstract

Over the past few years, outcomes and findings from several phase 1 clinical trials evaluating chimeric antigen receptor (CAR)-T cell therapies for glioblastoma (GBM) have been reported. For CAR-T cell therapy to succeed in GBM, several challenges must be overcome, including the immunosuppressive microenvironment (immunosuppressive cells, hypoxia, and metabolic constraints), antigen heterogeneity, and the anatomically isolated environment. To address these challenges, next-generation CAR-T cells-those engineered with additional functionalities-have been developed, and phase 1 clinical trials evaluating these next-generation CAR-T therapies for GBM have now been initiated. The development of CAR-T therapy for GBM has entered a new chapter. To date, the antitumor efficacy of CAR-T therapies still needs to be improved, and the high frequency of neurotoxicity remains a major issue that needs to be addressed; however, there is a growing anticipation that next-generation CAR-T therapies may provide clinical benefit to patients.

Journal for ImmunoTherapy of CancerVol. 14(4)
University of California, San Francisco (US), Parker Institute for Cancer Immunotherapy (US), Neurological Surgery (US)
National Institute of Neurological Disorders and Stroke
Openalex Percentile: Top 39%
CAR-T cell therapy research
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