Evidence map›Paper›PMID 31480372›Full record

ArticleCancers2019

Ultra-Mutation in

Valeria Barresi, Michele Simbolo, Andrea Mafficini, Maria Liliana Piredda, Maria Caffo, Salvatore Massimiliano Cardali, Antonino Germanò, Sara Cingarlini, Claudio Ghimenton, Aldo Scarpa

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

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  13. Recurrent oligodendroglioma with changed 1p/19q status.Neuropathology : official journal of the Japanese Society of Neuropathology · 2022
    Article
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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 2 institutions in 1 country.

Valeria BarresiDepartment of Diagnostics and Public Health, Section of Anatomical Pathology, University and Hospital Trust of Verona, 37134 Verona, Italy. valeria.barresi@univr.it.
Michele SimboloDepartment of Diagnostics and Public Health, Section of Anatomical Pathology, University and Hospital Trust of Verona, 37134 Verona, Italy.
Andrea MafficiniARC-Net Research Centre, University and Hospital Trust of Verona, 37134 Verona, Italy.
Maria Liliana PireddaDepartment of Diagnostics and Public Health, Section of Anatomical Pathology, University and Hospital Trust of Verona, 37134 Verona, Italy.
Maria CaffoDepartment of Biomedical and Dental Sciences and Morphofunctional Imaging, Section of Neurosurgery, University of Messina, 98125 Messina, Italy.
Salvatore Massimiliano CardaliDepartment of Biomedical and Dental Sciences and Morphofunctional Imaging, Section of Neurosurgery, University of Messina, 98125 Messina, Italy.
Antonino GermanòDepartment of Biomedical and Dental Sciences and Morphofunctional Imaging, Section of Neurosurgery, University of Messina, 98125 Messina, Italy.
Sara CingarliniDepartment of Medicine, Section of Medical Oncology, University and Hospital Trust Verona, 37134 Verona, Italy.
Claudio GhimentonDepartment of Pathology and Diagnostics, Section of Pathology, Hospital Trust Verona, 37134 Verona, Italy.
Aldo ScarpaDepartment of Diagnostics and Public Health, Section of Anatomical Pathology, University and Hospital Trust of Verona, 37134 Verona, Italy.
University of Verona · ITUniversity of Messina · IT

Funding

Associazione Italiana per la Ricerca sul Cancro 12182
6 · The paper itself

Abstract

backgroundGlioblastomas (GBMs) are classified into isocitrate dehydrogenase (

methodsSixteen

resultsEight (50%)

conclusionsWe identified a hyper-mutated subgroup among IDH-wt GBMs in adults < 55 years that had improved prognosis. Two cases were ultra-mutated and characterized by the presence of at least 25% giant cells, MMR mutations, and MSI. Since high TML has been associated with response to immune checkpoint inhibition in paediatric gliomas, the identification of a subtype of ultra-mutated IDH-wt GBM may have implications for immunotherapy.

Indexed as

giant cellsglioblastomaIDH wild-typemismatch repairPOLEtumour mutation load

Identifiers

PMID31480372
PMCPMC6770353
OpenAlexW2970023655

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.