Evidence map›Paper›PMID 17388946›Full record

ArticleBrain pathology (Zurich, Switzerland)2007

Nodule formation and desmoplasia in medulloblastomas-defining the nodular/desmoplastic variant and its biological behavior.

Charles S McManamy, Jane Pears, Claire L Weston, Zoltan Hanzely, James W Ironside, Roger E Taylor, Richard G Grundy, Steven C Clifford, David W Ellison, Clinical Brain Tumour Group

Open access · greenAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 146 citations in OpenAlex.

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  10. Medulloblastomas in Pediatric and Adults.Advances in experimental medicine and biology · 2023
    Article
  11. Review
  12. Review
  13. Review
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  15. Pathology, diagnostics, and classification of medulloblastoma.Brain pathology (Zurich, Switzerland) · 2020
    Review
  16. Article
  17. Article
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  19. Review
  20. Factors affecting survival of medulloblastoma in children: the changing concept of management.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2015
    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

10 authors at 5 institutions in 2 countries.

Charles S McManamyNorthern Institute for Cancer Research, University of Newcastle, and Department of Neuropathology, Newcastle-upon-Tyne Hospitals Trust, Newcastle-upon-Tyne, UK.
Jane Pears
Claire L Weston
Zoltan Hanzely
James W Ironside
Roger E Taylor
Richard G Grundy
Steven C Clifford
David W Ellison
Clinical Brain Tumour Group
Newcastle University · GBSingleton Hospital · GBUniversity of Newcastle Australia · AUUniversity of Nottingham · GBWestern General Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among the variants of medulloblastoma in the current WHO classification of nervous system tumors, the desmoplastic variant, which has been reported to constitute 5%-25% of pediatric medulloblastomas, is defined by its nodular collections of neurocytic cells bounded by desmoplastic internodular zones. We have studied the frequency, morphological features and biological behavior of medulloblastomas in two contemporaneous SIOP/UKCCSG trial cohorts of children with medulloblastomas, CNS9102 (n = 315) and CNS9204 (n = 35), focusing on tumors with nodular and desmoplastic phenotypes. In children aged 3-16 years (CNS9102), the nodular/desmoplastic medulloblastoma represented 5% of all tumors, while in infants aged <3 years (CNS9204) this variant represented 57% of medulloblastomas. Using iFISH to detect molecular cytogenetic abnormalities in medulloblastomas with a nodular architecture, we demonstrated distinct genetic profiles in desmoplastic and non-desmoplastic (classic and anaplastic) tumors; in particular, abnormalities of chromosome 17 occurred in the latter, but not the former. Significantly different outcomes were demonstrated for classic, nodular/desmoplastic and large cell/anaplastic medulloblastomas in both cohorts. In conclusion, the nodular/desmoplastic medulloblastoma appears to have clinical, genetic and biological characteristics that set it apart from other variants of this tumor.

Indexed as

AdolescentAge FactorsCerebellar NeoplasmsChildChild, PreschoolChromosome AberrationsFemaleHumansImmunohistochemistryInfantIn Situ Hybridization, FluorescenceMaleMedulloblastoma

Identifiers

PMID17388946
PMCPMC8095556
OpenAlexW1968985509

What OpenQuestion holds

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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.