Evidence map›Paper›PMID 39409893›Full record

ReviewCancers2024

Barriers to T Cell Functionality in the Glioblastoma Microenvironment.

Noor E Nader, Stephen C Frederico, Tracy Miller, Sakibul Huq, Xiaoran Zhang, Gary Kohanbash, Constantinos G Hadjipanayis

Abstract readReview
In one paragraph

Review in Cancers, 2024. 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
–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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
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  9. Review
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

7 authors.

Noor E NaderSchool of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0009-0006-2270-5521
Stephen C FredericoSchool of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0000-0003-0232-9187
Tracy MillerSchool of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Sakibul HuqDepartment of Neurological Surgery, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Xiaoran ZhangSloan Kettering Memorial Cancer Center, New York, NY 10065, USA.
Gary KohanbashSloan Kettering Memorial Cancer Center, New York, NY 10065, USA.ORCID 0000-0002-3953-8022
Constantinos G HadjipanayisDepartment of Neurological Surgery, University of Pittsburgh, Pittsburgh, PA 15213, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Medical Scientist Training ProgramT32GM144300 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RICHARD A STEINMAN, Russell S Schwartz · 2022 to 2026
$7.9M
NCI NIH HHS P30 CA008748NIGMS NIH HHS T32 GM144300
6 · The paper itself

Abstract

Glioblastoma (GBM) is an aggressive primary brain tumor depicted by a cold tumor microenvironment, low immunogenicity, and limited effective therapeutic interventions. Its location in the brain, a highly immune-selective organ, acts as a barrier, limiting immune access and promoting GBM dissemination, despite therapeutic interventions. Currently, chemotherapy and radiation combined with surgical resection are the standard of care for GBM treatment. Although immune checkpoint blockade has revolutionized the treatment of solid tumors, its observed success in extracranial tumors has not translated into a significant survival benefit for GBM patients. To develop effective immunotherapies for GBM, it is vital to tailor treatments to overcome the numerous immunosuppressive barriers that inhibit T cell responses to these tumors. In this review, we address the unique physical and immunological barriers that make GBM challenging to treat. Additionally, we explore potential therapeutic mechanisms, studied in central nervous system (CNS) and non-CNS cancers, that may overcome these barriers. Furthermore, we examine current and promising immunotherapy clinical trials and immunotherapeutic interventions for GBM. By highlighting the array of challenges T cell-based therapies face in GBM, we hope this review can guide investigators as they develop future immunotherapies for this highly aggressive malignancy.

Indexed as

brainCNSGBMglioblastomaT cell

Identifiers

PMID39409893
PMCPMC11476085

What OpenQuestion holds

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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.