Evidence map›Paper›PMID 39202398›Full record

ReviewGenes2024

Pediatric Hemispheric High-Grade Gliomas and H3.3-G34 Mutation: A Review of the Literature on Biological Features and New Therapeutic Strategies.

Marta Bonada, Matilde Pittarello, Emerson De Fazio, Alessandro Gans, Paolo Alimonti, Hasan Slika, Federico Legnani, Francesco Di Meco, Betty Tyler

Abstract readReview
In one paragraph

Review in Genes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. 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

9 authors.

Marta BonadaDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133 Milan, Italy.
Matilde PittarelloDepartment of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.ORCID 0009-0001-7927-0825
Emerson De FazioDepartment of Medicine, Vita-Salute San Raffaele University School of Medicine, 20132 Milan, Italy.
Alessandro GansDepartment of Oncology and Hemato-Oncology, University of Milan School of Medicine, Via Rudini 8, 20122 Milan, Italy.ORCID 0000-0002-6222-8479
Paolo AlimontiDepartment of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02120, USA.
Hasan SlikaDepartment of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.ORCID 0000-0003-4597-3642
Federico LegnaniDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133 Milan, Italy.ORCID 0000-0002-3547-1510
Francesco Di MecoDepartment of Neurosurgery, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133 Milan, Italy.ORCID 0000-0001-6213-5793
Betty TylerDepartment of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.ORCID 0000-0001-9800-6969

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pediatric high-grade glioma (pHGG) encompasses a wide range of gliomas with different genomic, epigenomic, and transcriptomic features. Almost 50% of pHGGs present a mutation in genes coding for histone 3, including the subtype harboring the H3.3-G34 mutation. In this context, histone mutations are frequently associated with mutations in

Indexed as

Brain NeoplasmsGliomaHistonesMutationChildEpigenesis, GeneticHumansTumor MicroenvironmentHistonesgliomahigh-gradehistone mutationimmunotherapypediatrictargeted therapy

Identifiers

PMID39202398
PMCPMC11353413

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.