Evidence map›Paper›PMID 28856550›Full record

ArticleJournal of neuro-oncology2017

Frequency and clinical significance of chromosome 7 and 10 aneuploidies, amplification of the EGFR gene, deletion of PTEN and TP53 genes, and 1p/19q deficiency in a sample of adult patients diagnosed with glioblastoma from Southern Brazil.

Dayane B Koshiyama, Patrícia Trevisan, Carla Graziadio, Rafael F M Rosa, Bibiana Cunegatto, Juliete Scholl, Valentina O Provenzi, Alexandre P de Sá, Fabiano P Soares, Maíra C Velho and 3 more

Abstract read
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In one paragraph

Article in Journal of neuro-oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.3field-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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Clinical and Molecular Characterization of Adult Glioblastomas in Southern Brazil.Journal of neuropathology and experimental neurology · 2019
    Article
  12. Article
  13. Favorable prognostic impact ofNeuro-oncology advances
    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

13 authors at 4 institutions in 1 country.

Dayane B KoshiyamaGraduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.
Patrícia TrevisanGraduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.
Carla GraziadioClinical Genetics, UFCSPA and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil.
Rafael F M RosaGraduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.
Bibiana CunegattoGraduation in Biomedicine, UFCSPA, Porto Alegre, RS, Brazil.
Juliete SchollGraduation in Biomedicine, UFCSPA, Porto Alegre, RS, Brazil.
Valentina O ProvenziDepartment of Pathology, Grupo Hospitalar Conceição (GHC), Porto Alegre, RS, Brazil.
Alexandre P de SáGraduation in Medicine, UFCSPA, Porto Alegre, RS, Brazil.
Fabiano P SoaresDepartment of Neurosurgery, Hospital Beneficência Portuguesa, Porto Alegre, RS, Brazil.
Maíra C VelhoDepartment of Neurosurgery, Hospital Beneficência Portuguesa, Porto Alegre, RS, Brazil.
Nelson de A P FilhoDepartment of Neurosurgery, Hospital Beneficência Portuguesa, Porto Alegre, RS, Brazil.
Ceres A OliveiraInstitute of Education and Research, Hospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Paulo R G ZenGraduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil. paulozen@ufcspa.edu.br.ORCID http://orcid.org/0000-0002-7628-4877
Universidade Federal de Ciências da Saúde de Porto Alegre · BRBeneficência Portuguesa de São Paulo · BRGrupo Hospitalar Conceição · BRHospital Moinhos de Vento · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma stands out as the most frequent central nervous system neoplasia, presenting a poor prognosis. The aim of this study was to verify the frequency and clinical significance of the aneuploidy of chromosomes 7 and 10, EGFR amplification, PTEN and TP53 deletions and 1p/19q deficiency in adult patients diagnosed with glioblastoma. The sample consisted of 40 patients treated from November 2011 to March 2015 at two major neurosurgery services from Southern Brazil. Molecular cytogenetic analyses of the tumor were performed through fluorescent in situ hybridization (FISH). The clinical features evaluated consisted of age, sex, tumor location, clinical symptoms, family history of cancer, type of resection and survival. The mean age of the patients was 59.3 years (ranged from 41 to 83). Most of them were males (70%). The median survival was 145 days. Chromosome 10 monosomy was detected in 52.5% of the patients, chromosome 7 polysomy in 50%, EGFR amplification in 42.5%, PTEN deletion in 35%, TP53 deletion in 22.5%, 1p deletion in 5% and 19q deletion in 7.5%. Age was shown to be a prognostic factor, and patients with lower age presented higher survival (p = 0.042). TP53 and PTEN deletions had a negative impact on survival (p = 0.011 and p = 0.037, respectively). Our data suggest that TP53 and PTEN deletions may be associated with a poorer prognosis. These findings may have importance over prognosis determination and choice of the therapy to be administered.

Indexed as

AdultAgedAged, 80 and overAneuploidyBrain NeoplasmsBrazilChromosomes, Human, Pair 1Chromosomes, Human, Pair 10Chromosomes, Human, Pair 7ErbB ReceptorsFemaleGlioblastomaHumansKaplan-Meier EstimateMaleMiddle AgedEGFR protein, humanErbB ReceptorsPTEN PhosphohydrolasePTEN protein, humanTP53 protein, humanTumor Suppressor Protein p531p19q codeletionEGFRFISHGlioblastomaPTENSurvivalTP53

Identifiers

PMID28856550
OpenAlexW2752713079

What OpenQuestion holds

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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.