Evidence map›Paper›PMID 32771057›Full record

ArticleActa neuropathologica communications2020

Clinical, radiological and molecular characterization of intramedullary astrocytomas.

Laetitia Lebrun, Barbara Meléndez, Oriane Blanchard, Nancy De Nève, Claude Van Campenhout, Julie Lelotte, Danielle Balériaux, Matteo Riva, Jacques Brotchi, Michaël Bruneau and 4 more

Open access · goldAbstract read
In one paragraph

Article in Acta neuropathologica communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Astrocytomas of the spinal cord.Neuro-oncology advances · 2024
    Review
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  16. Review
  17. Analyses of DNA Methylation Profiling in the Diagnosis of Intramedullary Astrocytomas.Journal of neuropathology and experimental neurology · 2021
    Article
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

14 authors at 4 institutions in 3 countries.

Laetitia LebrunDepartment of Pathology, Erasme University Hospital, Université Libre de Bruxelles (ULB), 808 Route de Lennik, B-1070, Brussels, Belgium.ORCID 0000-0002-5663-8180
Barbara MeléndezDepartment of Pathology, Erasme University Hospital, Université Libre de Bruxelles (ULB), 808 Route de Lennik, B-1070, Brussels, Belgium.
Oriane BlanchardDepartment of Pathology, Erasme University Hospital, Université Libre de Bruxelles (ULB), 808 Route de Lennik, B-1070, Brussels, Belgium.
Nancy De NèveDepartment of Pathology, Erasme University Hospital, Université Libre de Bruxelles (ULB), 808 Route de Lennik, B-1070, Brussels, Belgium.
Claude Van CampenhoutDepartment of Pathology, Erasme University Hospital, Université Libre de Bruxelles (ULB), 808 Route de Lennik, B-1070, Brussels, Belgium.
Julie LelotteDepartment of Pathology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain (UCLouvain), Brussels, Belgium.
Danielle BalériauxDepartment of Neuroradiology, Erasme University Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Matteo RivaDepartment of Neurosurgery, Mont-Godinne University Hospital, UcL Namur, Yvoir, Belgium.
Jacques BrotchiDepartment of Neurosurgery, Erasme University Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Michaël BruneauDepartment of Neurosurgery, Erasme University Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Olivier De WitteDepartment of Neurosurgery, Erasme University Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Christine DecaesteckerDIAPath, Center for Microscopy and Molecular Imaging, ULB, Gosselies, Belgium.
Nicky D'HaeneDepartment of Pathology, Erasme University Hospital, Université Libre de Bruxelles (ULB), 808 Route de Lennik, B-1070, Brussels, Belgium.
Isabelle SalmonDepartment of Pathology, Erasme University Hospital, Université Libre de Bruxelles (ULB), 808 Route de Lennik, B-1070, Brussels, Belgium. isabelle.salmon@erasme.ulb.ac.be.
Université Libre de Bruxelles · BECHU Dinant Godinne UCL Namur · BECliniques Universitaires Saint-Luc · BEVIB-UAntwerp Center for Molecular Neurology · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intramedullary astrocytomas (IMAs) are rare tumors, and few studies specific to the molecular alterations of IMAs have been performed. Recently, KIAA1549-BRAF fusions and the H3F3A p.K27M mutation have been described in low-grade (LG) and high-grade (HG) IMAs, respectively. In the present study, we collected clinico-radiological data and performed targeted next-generation sequencing for 61 IMAs (26 grade I pilocytic, 17 grade II diffuse, 3 LG, 3 grade III and 12 grade IV) to identify KIAA1549-BRAF fusions and mutations in 33 genes commonly implicated in gliomas and the 1p/19q regions. One hundred seventeen brain astrocytomas were analyzed for comparison. While we did not observe a difference in clinico-radiological features between LG and HG IMAs, we observed significantly different overall survival (OS) and event-free survival (EFS). Multivariate analysis showed that the tumor grade was associated with better OS while EFS was strongly impacted by tumor grade and surgery, with higher rates of disease progression in cases in which only biopsy could be performed. For LG IMAs, EFS was only impacted by surgery and not by grade. The most common mutations found in IMAs involved TP53, H3F3A p.K27M and ATRX. As in the brain, grade I pilocytic IMAs frequently harbored KIAA1549-BRAF fusions but with different fusion types. Non-canonical IDH mutations were observed in only 2 grade II diffuse IMAs. No EGFR or TERT promoter alterations were found in IDH wild-type grade II diffuse IMAs. These latter tumors seem to have a good prognosis, and only 2 cases underwent anaplastic evolution. All of the HG IMAs presented at least one molecular alteration, with the most frequent one being the H3F3A p.K27M mutation. The H3F3A p.K27M mutation showed significant associations with OS and EFS after multivariate analysis. This study emphasizes that IMAs have distinct clinico-radiological, natural evolution and molecular landscapes from brain astrocytomas.

Indexed as

AdolescentAdultAgedAstrocytomaChildChild, PreschoolFemaleHumansMaleMiddle AgedProgression-Free SurvivalSpinal Cord NeoplasmsYoung AdultIntramedullary astrocytomas-glial tumor-spinal cord-targeted next-generation sequencing-H3F3A K27M-KIAA1549-BRAF

Identifiers

PMID32771057
PMCPMC7414698
OpenAlexW3048285927

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.