Evidence map›Paper›PMID 19387655›Full record

ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2009

Survival following treatment for intracranial ependymoma: a review.

G Tamburrini, M D'Ercole, B L Pettorini, M Caldarelli, L Massimi, C Di Rocco

Abstract readReview
PubMed Publisher
In one paragraph

Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Quantitative imaging analysis of posterior fossa ependymoma location in children.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2016
    Article
  10. Article
  11. Article
  12. Chromosomal anomalies and prognostic markers for intracranial and spinal ependymomas.Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia · 2012
    Review
  13. Cerebellopontine angle ependymoma in a 2-year- old child.Journal of neurosciences in rural practice · 2012
    Article
  14. Article
  15. Article
  16. Article
  17. Challenging issues in pediatric oncology.Nature reviews. Clinical oncology · 2011
    Review
  18. Pediatric anaplastic parenchymal ependymoma: case report.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2011
    Article
  19. Article
  20. Posterior fossa ependymomas: new radiological classification with surgical correlation.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2010
    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

6 authors.

G TamburriniPediatric Neurosurgery, Institute of Neurosurgery, Catholic University Medical School, Largo A. Gemelli, 8, 00168, Rome, Italy. gianpiero.tamburrini@rm.unicatt.it
M D'Ercole
B L Pettorini
M Caldarelli
L Massimi
C Di Rocco

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The actual definition of survival rates following treatment for intracranial ependymomas is substantially influenced by the strict interaction among different factors. Age, location, and grading, for example, act together, negatively influencing the prognosis of younger children also invariably influenced by the more demanding role of surgery and the still limited use, up to recently, of radiotherapy under 3 years of age. In the same direction, the worse prognosis in most series of infratentorial ependymomas if compared with their supratentorial counterpart should be cautiously considered, midline posterior fossa tumors having completely different implications from those originating or predominantly extending to the cerebellopontine angle, where the extent of surgery has more invariably to compare with patients' quality of life. New radiotherapic regimens and their applications in infancy are promisingly demonstrating an improvement of present prognostic criteria, with the limit of still insufficient information on their long-term secondary effects. Similarly, molecular biology research studies, though still in their preclinical stage, are prompting to change the concept of a substantially chemoresistant tumor helping to stratify these lesions with the final aim of targeted pharmacological therapies. In the present review paper, we investigated singularly the role that the more commonly considered prognostic factors have had in the literature on survival of children affected by intracranial ependymomas, trying to elucidate their cumulative effect on the actual knowledge of this issue.

Indexed as

Brain NeoplasmsChildEpendymomaHumansPrognosisTreatment Outcome

Identifiers

What OpenQuestion holds

Textmetadata
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.