Evidence map›Paper›PMID 38995395›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2024

Doing more with less: surgical results of pediatric posterior fossa tumors from a single center in Latin America.

Cleiton Formentin, Lucas de Souza Rodrigues Dos Santos, Leo Gordiano Matias, Dayvid Leonardo de Castro Oliveira, Marcelo Ferreira Sabba, Andrei Fernandes Joaquim, Helder Tedeschi, Enrico Ghizoni

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing 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

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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

1 citing paper in PubMed.

  1. Hydrocephalus in pediatric posterior fossa tumors: predictors and outcomes from a single center in Latin America.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
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4 · The record

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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

8 authors.

Cleiton FormentinDepartment of Neurosurgery, Boldrini Children's Hospital, Gabriel Porto St - Cidade Universitária, 1270 Dr, São Paulo, Campinas, 13083-210, Brazil. cleitonformentin@gmail.com.
Lucas de Souza Rodrigues Dos SantosDeparment of Neurology, University of Campinas, Campinas-SP, Brazil.
Leo Gordiano MatiasDepartment of Neurosurgery, Boldrini Children's Hospital, Gabriel Porto St - Cidade Universitária, 1270 Dr, São Paulo, Campinas, 13083-210, Brazil.
Dayvid Leonardo de Castro OliveiraDeparment of Neurology, University of Campinas, Campinas-SP, Brazil.
Marcelo Ferreira SabbaDeparment of Neurology, University of Campinas, Campinas-SP, Brazil.
Andrei Fernandes JoaquimDepartment of Neurosurgery, Boldrini Children's Hospital, Gabriel Porto St - Cidade Universitária, 1270 Dr, São Paulo, Campinas, 13083-210, Brazil.
Helder TedeschiDepartment of Neurosurgery, Boldrini Children's Hospital, Gabriel Porto St - Cidade Universitária, 1270 Dr, São Paulo, Campinas, 13083-210, Brazil.
Enrico GhizoniDepartment of Neurosurgery, Boldrini Children's Hospital, Gabriel Porto St - Cidade Universitária, 1270 Dr, São Paulo, Campinas, 13083-210, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWe aim to report the epidemiology, surgical outcomes, and survival rates of pediatric patients with posterior fossa tumors in a large single-center case series.

methodsA retrospective analysis was conducted on pediatric patients who underwent surgical treatment for posterior fossa tumors between January 2011 and January 2019.

resultsA total of 135 pediatric patients, with an average age of 7.5 years at diagnosis and a mean follow-up of 35.7 months, were included in the study. Most tumors were located within the midline, with ventriculomegaly observed in 71.4% of the patients. Pilocytic astrocytomas encompassed the majority of tumors (34.1%), followed by medulloblastomas (27.4%) and ependymomas (11.8%). Gross total resection (GTR) was achieved in 71.8% of the patients, with a recurrence rate of 20%. Surgical complications were observed in 25.9% of the patients. GTR significantly impacted 5-year overall survival (OS) and 4-year progression-free survival (PFS) in patients with posterior fossa tumors. Patients who underwent GTR had a 5-year OS of 89.7%, compared to 72.7% for near-total resection and 70.8% for subtotal resection. The 4-year PFS for patients who underwent GTR was 82.5%, whereas it was 63.6% for patients who underwent near-total resection and 54.2% for patients who underwent subtotal resection.

conclusionSurgical resection remains the main treatment for pediatric posterior fossa tumors, and higher resection rates are linked to better survival outcomes. Despite limited resources for molecular diagnosis, our institution has demonstrated that a specialized neurooncological center with a high surgical volume can still achieve favorable survival outcomes for these patients.

Indexed as

Infratentorial NeoplasmsNeurosurgical ProceduresAdolescentChildChild, PreschoolFemaleHumansInfantLatin AmericaMaleRetrospective StudiesSurvival RateTreatment OutcomeEpendymomaInfratentorial neoplasmsMedulloblastomaPilocytic astrocytoma

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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.