Evidence map›Paper›PMID 26537911›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2016

Pediatric glioblastoma: a single institution experience.

Marina Nikitović, Dragana Stanić, Tatjana Pekmezović, Milica Skender Gazibara, Jelena Bokun, Lejla Paripović, Danica Grujičić, Milan Sarić, Ivana Mišković

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  7. Review
  8. Review
  9. The role of sex genotype in paediatric CNS tumour incidence and survival.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
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  15. H3K27M, IDH1, and ATRX expression in pediatric GBM and their clinical and prognostic significance.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2019
    Article
  16. Successful treatment of aBMJ case reports · 2019
    Article
  17. Article
  18. Evaluating extent of resection in pediatric glioblastoma: a multiple propensity score-adjusted population-based analysis.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2016
    Article
  19. Childhood Pineal Glioblastoma: Case Report.Journal of pediatric neurosciences
    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.

Marina NikitovićFaculty of Medicine, University of Belgrade, Dr Subotica 8, 11000, Belgrade, Serbia. marina.nikitovic@ncrc.ac.rs.ORCID http://orcid.org/0000-0001-7272-9587
Dragana StanićInstitute for Oncology and Radiology of Serbia, Clinic for Radiation Oncology, Pasterova 14, 11000, Belgrade, Serbia.
Tatjana PekmezovićFaculty of Medicine, University of Belgrade, Dr Subotica 8, 11000, Belgrade, Serbia.
Milica Skender GazibaraFaculty of Medicine, University of Belgrade, Dr Subotica 8, 11000, Belgrade, Serbia.
Jelena BokunInstitute for Oncology and Radiology of Serbia, Clinic for Radiation Oncology, Pasterova 14, 11000, Belgrade, Serbia.
Lejla ParipovićInstitute for Oncology and Radiology of Serbia, Clinic for Pediatric Oncology, Pasterova 14, 11000, Belgrade, Serbia.
Danica GrujičićFaculty of Medicine, University of Belgrade, Dr Subotica 8, 11000, Belgrade, Serbia.
Milan SarićInstitute for Oncology and Radiology of Serbia, Clinic for Radiation Oncology, Pasterova 14, 11000, Belgrade, Serbia.
Ivana MiškovićInstitute for Oncology and Radiology of Serbia, Clinic for Radiation Oncology, Pasterova 14, 11000, Belgrade, Serbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe aim of this study was to evaluate characteristics of childhood glioblastoma multiforme, effectiveness of treatment modalities, and detect factors related to outcome.

methodsA detailed analysis was performed on a series of 15 patients treated between 2000 and 2013, based on their clinical, radiologic, pathologic, treatment, and follow-up data.

resultsMedian survival time of children with glioblastoma was 13.5 months. One- and 2-year overall survival probabilities were 66.7 and 20 %, respectively. There were no significant differences in survival based on patients' gender, age, disease presentation with or without epileptic seizures, signs/symptoms of increased intracranial pressure, or tumor location. The presence of neurological deficit initially, as well as prior to radiotherapy, which was quantified by neurologic function score (NFS), had an impact on overall survival. Children with NFS 0 lived longer compared to others (p = 0.001). Survival of children that underwent gross total resection was longer than that of children that underwent subtotal resection (p = 0.030). Mean survival time of children with gross total resection was 73.5 months, compared to 13 months in children with subtotal resection. There was no significant correlation between outcome and type of radiotherapy. In four patients with gigantocellular glioblastoma, we found no evidence of a better prognosis. Two long-term survivors were recorded. Both of them underwent gross total resection and were assigned a NFS 0.

conclusionsGross total resection is essential for longer overall survival among pediatric patients with glioblastoma and offers a possibility for long-term survival. Severity of neurologic symptoms quantified by NFS can be considered as a potential predictor of outcome.

Indexed as

Brain NeoplasmsGlioblastomaTreatment OutcomeAdolescentChildChild, PreschoolCombined Modality TherapyFemaleHumansKaplan-Meier EstimateMaleRetrospective StudiesSurvival RateBrain tumorsChildrenGlioblastoma multiformeTreatment

Identifiers

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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.