Evidence map›Paper›PMID 41922085›Full record

ReviewJournal for immunotherapy of cancer2026

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

Junya Yamaguchi, Hideho Okada

Abstract readReview
In one paragraph

Review in Journal for immunotherapy of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Junya YamaguchiDepartment of Neurological Surgery, University of California San Francisco, San Francisco, California, USA.ORCID http://orcid.org/0000-0002-4344-5750
Hideho OkadaDepartment of Neurological Surgery, University of California San Francisco, San Francisco, California, USA hideho.okada@ucsf.edu.ORCID http://orcid.org/0000-0003-0076-9920

Funding

Preclinical development of breakthrough immunotherapy for brain tumorsR35NS142982 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Hideho Okada · 2026 to 2026
$943k
NINDS NIH HHS R35 NS142982
6 · The paper itself

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.

Indexed as

Brain NeoplasmsGlioblastomaImmunotherapy, AdoptiveReceptors, Antigen, T-CellReceptors, Chimeric AntigenT-LymphocytesAnimalsHumansReceptors, Antigen, T-CellReceptors, Chimeric AntigenAdoptive cell therapy - ACTCentral Nervous System CancerChimeric antigen receptor - CARImmunotherapy

Identifiers

PMID41922085
PMCPMC13052789

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.