Evidence map›Paper›PMID 15332330›Full record

ArticleJournal of neuro-oncology2004

Multivariate analysis of clinical prognostic factors in children with intracranial ependymomas.

Tang-Her Jaing, Huei-Shyong Wang, Pei-Kwei Tsay, Chen-Kan Tseng, Shih-Ming Jung, Kuang-Lin Lin, Tai-Ngar Lui

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Journal of neuro-oncology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 27% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Histologic grade and extent of resection are associated with survival in pediatric spinal cord ependymomas.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2013
    Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Pediatric anaplastic parenchymal ependymoma: case report.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2011
    Article
  14. Article
  15. Surgical management of supratentorial ependymomas.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2009
    Review
  16. Survival following treatment for intracranial ependymoma: a review.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2009
    Review
  17. Three-dimensional conformal radiation therapy for ependymoma.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2009
    Article
  18. Classification and controversies in pathology of ependymomas.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2009
    Review
  19. Outcome of teenagers and young adults with ependymoma: the Royal Marsden experience.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2009
    Article
  20. 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

7 authors at 3 institutions in 2 countries.

Tang-Her JaingDivision of Hematology and Oncology, Department of Pediatrics, Chang Gung Children's Hospital, Taoyuan, Taiwan. jaing001@cgmh.org.tw
Huei-Shyong Wang
Pei-Kwei Tsay
Chen-Kan Tseng
Shih-Ming Jung
Kuang-Lin Lin
Tai-Ngar Lui
Chang Gung Children's Hospital · TWChang Gung Memorial Hospital · TWChang Gung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The optimal postoperative management of pediatric intracranial ependymomas is controversial. We analyzed clinical prognostic factors for their influence on outcome in such children. Our retrospective series included 15 with supratentorial and 28 with infratentorial tumors. Twenty ependymomas were grade II, and 23 were anaplastic. Complete resection was performed in 18 patients, incomplete resection in 19, and stereotactic biopsy in 6. Radiotherapy was done in 31 patients and chemotherapy in 13. The surviving patients have been followed 8-232 months (median: 69 months). The median survival time was 30 months, and 5-year overall survival and progression-free survival rates were 53.9% and 45.9%, respectively. By tumor site: supratentorial, 56.6% and 50.9%; infratentorial, 52.3% and 42.5%. Multivariate analysis identified complete resection (5-year progression-free survival, 71.8%) and age <3 years old as significant favorable and adverse prognostic features (relative risk, 2.59; 95% CI, 1.05-6.38), respectively. Twenty-six children relapsed 1-107 months after diagnosis (median: 12 months). Relapses were local in 22 cases, and combined local and distant in three cases. Only one of 15 patients with supratentorial tumors developed isolated spinal metastasis. Failure at the primary site is the major obstacle to improve cure rates. The extent of surgical resection and age were the only statistically significant prognostic factors.

Indexed as

AdolescentAge FactorsChildChild, PreschoolEpendymomaFemaleHumansInfantInfratentorial NeoplasmsMaleMultivariate AnalysisNeoplasm Recurrence, LocalPrognosisRetrospective StudiesSex FactorsSupratentorial Neoplasms

Identifiers

PMID15332330
OpenAlexW2088919057

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.