Evidence map›Paper›PMID 36890859›Full record

ArticleClinical & translational immunology2023

Human EGFRvIII chimeric antigen receptor T cells demonstrate favorable safety profile and curative responses in orthotopic glioblastoma.

Rebecca C Abbott, Melinda Iliopoulos, Katherine A Watson, Valeria Arcucci, Margareta Go, Hannah E Hughes-Parry, Pete Smith, Melissa J Call, Ryan S Cross, Misty R Jenkins

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
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

9 citing papers in PubMed, 14 citations in OpenAlex.

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  8. Treatment advances in high-grade gliomas.Frontiers in oncology · 2024
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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

10 authors at 3 institutions in 2 countries.

Rebecca C AbbottImmunology Division The Walter and Eliza Hall Institute of Medical Research Parkville VIC Australia.ORCID https://orcid.org/0000-0002-0897-7874
Melinda IliopoulosImmunology Division The Walter and Eliza Hall Institute of Medical Research Parkville VIC Australia.ORCID https://orcid.org/0000-0002-7229-4189
Katherine A WatsonImmunology Division The Walter and Eliza Hall Institute of Medical Research Parkville VIC Australia.ORCID https://orcid.org/0000-0002-8531-9883
Valeria ArcucciImmunology Division The Walter and Eliza Hall Institute of Medical Research Parkville VIC Australia.ORCID https://orcid.org/0000-0001-8508-1580
Margareta GoStructural Biology Division The Walter and Eliza Hall Institute of Medical Research Parkville VIC Australia.ORCID https://orcid.org/0000-0001-5695-2439
Hannah E Hughes-ParryImmunology Division The Walter and Eliza Hall Institute of Medical Research Parkville VIC Australia.ORCID https://orcid.org/0000-0001-9843-1551
Pete SmithMyrio Therapeutics Blackburn North, Melbourne VIC Australia.
Melissa J CallThe Department of Medical Biology University of Melbourne Parkville VIC Australia.ORCID https://orcid.org/0000-0001-7684-5841
Ryan S CrossImmunology Division The Walter and Eliza Hall Institute of Medical Research Parkville VIC Australia.ORCID https://orcid.org/0000-0002-8573-8551
Misty R JenkinsImmunology Division The Walter and Eliza Hall Institute of Medical Research Parkville VIC Australia.ORCID https://orcid.org/0000-0001-6564-2715
Walter and Eliza Hall Institute of Medical Research · AUThe University of Melbourne · AUBlackburn College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Glioblastoma is a highly aggressive and fatal brain malignancy, and effective targeted therapies are required. The combination of standard treatments including surgery, chemotherapy and radiotherapy is not curative. Chimeric antigen receptor (CAR) T cells are known to cross the blood-brain barrier, mediating antitumor responses. A tumor-expressed deletion mutant of the epidermal growth factor receptor (EGFRvIII) is a robust CAR T cell target in glioblastoma. Here, we show our Methods: The GCT02 binding epitope was predicted using Deep Mutational Scanning (DMS). GCT02 CAR T cell cytotoxicity was investigated in three glioblastoma models Results: The GCT02 binding location was predicted to be located at a shared region of EGFR and EGFRvIII; however, the Conclusion: This study demonstrates the preclinical functionality of a highly specific CAR targeting EGFRvIII on human cells. This CAR could be an effective treatment for glioblastoma and warrants future clinical investigation.

Indexed as

CAR T cellschimeric antigen receptorEGFRvIIIglioblastomaimmunotherapy

Identifiers

PMID36890859
PMCPMC9986233
OpenAlexW4323285828

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.