Evidence map›Paper›PMID 18710393›Full record

ArticleBrain pathology (Zurich, Switzerland)2009

Interphase cytogenetics for 1p19q and t(1;19)(q10;p10) may distinguish prognostically relevant subgroups in extraventricular neurocytoma.

Fausto J Rodriguez, Renan A Mota, Bernd W Scheithauer, Caterina Giannini, Hilary Blair, Kent C New, Kevin J Wu, Dennis W Dickson, Robert B Jenkins

Open access · greenAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
  2. Article
  3. A rare case of atypical spinal neurocytoma with EGFR mutation in a 12-year-old boy.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Article
  4. Review
  5. Review
  6. Cerebellar Liponeurocytoma: Relevant Clinical Cytogenetic Findings.Journal of pathology and translational medicine · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Pathologic features and clinical outcome of central neurocytoma: analysis of 15 cases.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2012
    Article
  12. A rare case of a pediatric extraventricular neurocytoma: case report and review of the literature.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2012
    Review
  13. Article
  14. Review
  15. Re: Diffuse leptomeningeal glioneuronal tumors: a new entity?Brain pathology (Zurich, Switzerland) · 2009
    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

9 authors at 3 institutions in 1 country.

Fausto J RodriguezDepartment of Laboratory Medicine, Mayo Clinic, Rochester, MN 55905, USA. rodriguez.fausto@mayo.edu
Renan A Mota
Bernd W Scheithauer
Caterina Giannini
Hilary Blair
Kent C New
Kevin J Wu
Dennis W Dickson
Robert B Jenkins
Mayo Clinic · USMayo Clinic in Arizona · USMayo Clinic in Florida · US

Funding

Research Training Program in Neuro-OncologyT32NS007494 · NINDS · MAYO CLINIC ROCHESTER · PI O'NEILL, BRIAN PATRICK · 2002 to 2014
$1.4M
NINDS NIH HHS T32 NS007494NINDS NIH HHS T32 NS07494-04
6 · The paper itself

Abstract

Co-deletion of chromosome arms 1p and 19q, characteristic of oligodendroglial tumors, was recently found to be mediated by t(1;19)(q10;p10). To evaluate the prevalence of 1p19q co-deletion and t(1;19) in extraventricular neurocytomas (EVN), we studied tumors from 23 patients, including 13 females and 10 males (median age at diagnosis 34 years, range 2-76 years). Fluorescence in situ hybridization (FISH) studies were performed with probes targeting 1p36/1q25 and 19q13/19p13 to assess for 1p19q co-deletion, as well as chromosome 1 alpha-satellite and 19p12 to detect t(1;19)(q10;p10). FISH was successful in 21 (91%) cases and demonstrated 1p19q co-deletion in five cases (24%) or isolated 1p loss in two cases (10%). Evidence for t(1;19) was found in four (of five) cases with 1p19q co-deletion. Three tumors with 1p19q loss and t(1;19) demonstrated atypical histologic features, compared with one (of 17) tumors without 1p19q co-deletion (P = 0.01, Fisher exact test). In addition, tumors with t(1;19) showed increased mitotic activity compared with tumors without t(1;19) (P = 0.045; Wilcoxon rank sum test). The four patients with t(1;19) developed tumor recurrence (n = 3), or expired (n = 2) 3.5 to 5.5 years after first resection. These results suggest that 1p19q loss and t(1;19) occur in a subset of EVN, and may be associated with aggressive histology in these tumors.

Indexed as

Chromosome DeletionTranslocation, GeneticAdolescentAdultAgedBrain NeoplasmsChildChild, PreschoolChromosomes, Human, Pair 1Chromosomes, Human, Pair 19Cytogenetic AnalysisFemaleGenetic Predisposition to DiseaseHumansImmunohistochemistryIn Situ Hybridization, Fluorescence

Identifiers

PMID18710393
PMCPMC2742575
OpenAlexW2083862793

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.