Evidence map›Paper›PMID 29214340›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2018

Management and outcomes of treating pediatric medulloblastoma: an eight years' experience in an Iranian pediatric center.

Azim Mehrvar, Maryam Tashvighi, Amir Abbas Hedayati Asl, Naghmeh Niktoreh-Mofrad, Narjes Mehrvar, Negar Afsar, Ali Naderi, Mardawig Allebouyeh, Ibrahim Qaddoumi, Mohammad Faranoush

Abstract read
PubMed Publisher
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Current Strategies for Management of Medulloblastoma.Diagnostics (Basel, Switzerland) · 2023
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. National cancer registry and broad institutional cooperation: turning points in treating childhood medulloblastoma in Iran.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2018
    Article
  9. Letter to the editor Management and outcome of treating pediatric medulloblastoma.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Azim MehrvarMAHAK Pediatric Cancer Treatment and Research Center, Tehran, Iran.
Maryam TashvighiMAHAK Pediatric Cancer Treatment and Research Center, Tehran, Iran.
Amir Abbas Hedayati AslMAHAK Pediatric Cancer Treatment and Research Center, Tehran, Iran.
Naghmeh Niktoreh-MofradMAHAK Pediatric Cancer Treatment and Research Center, Tehran, Iran. naghmeh.niktoreh@uk-essen.de.ORCID 0000-0002-5032-4789
Narjes MehrvarCancer Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Negar AfsarMAHAK Pediatric Cancer Treatment and Research Center, Tehran, Iran.
Ali NaderiMAHAK Pediatric Cancer Treatment and Research Center, Tehran, Iran.
Mardawig AllebouyehMAHAK Pediatric Cancer Treatment and Research Center, Tehran, Iran.
Ibrahim QaddoumiDepartment of Global Pediatric Medicine, St. Jude Children's Research Hospital, Memphis, TN, USA.
Mohammad FaranoushMAHAK Pediatric Cancer Treatment and Research Center, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe clinical management of pediatric medulloblastoma requires a multidisciplinary approach, which can be challenging, especially in low- and middle-income countries. The aim of this study was to identify current challenges and describe the treatment and outcomes of Iranian pediatric patients with medulloblastoma who were referred to our center in Tehran, Iran.

methodsOur retrospective review included 126 patient records from April 2007 to May 2015. The records were analyzed for epidemiologic features, treatment modalities, overall survival, and progression-free survival. Data were analyzed using SPSS 22.0 software.

resultsMedian age at diagnosis was 6 years (male:female ratio, 2.3:1). At the time of diagnosis, 7 patients were 2 years or younger, and 76 (60.3%) were categorized as having high-risk disease. Overall, 100 patients had gross or near-total surgical resection. Cerebral spinal fluid involvement was detected in 22.2% of the patients tested, and spinal involvement was detected in 25% of the patients who underwent spinal MRI. Metastasis stages at the time of diagnosis were as follows: M0: 48.4% patients, M1: 16.7%, M2: 5.5%, and M3: 21.4%. Median times of follow-up and progression-free survival were 16 and 12 months, respectively. Probability of 7-year overall survival and progression-free survival were 59 and 53.8%, respectively.

conclusionsResults of the current retrospective study emphasize the need for implementing measures to improve outcome for our patients with medulloblastoma. Such measures include a multidisciplinary approach, unified national treatment guidelines, better disease and metastasis staging, twinning initiatives, and seeking a second opinion when needed.

Indexed as

Disease ManagementHospitals, PediatricCerebellar NeoplasmsChildChild, PreschoolFemaleHumansIranLongitudinal StudiesMagnetic Resonance ImagingMaleMedulloblastomaRetrospective StudiesTreatment OutcomeCentral nervous system neoplasmsManagementMedulloblastomaPediatrics

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.