Evidence map›Paper›PMID 41149493›Full record

ReviewCurrent oncology (Toronto, Ont.)2025

Bevacizumab in Pediatric Neuro-Oncology.

Jacob Silverman, Sayanthen Sathyakumar, Hallie Coltin, Sebastien Perreault, Nada Jabado, Eric Bouffet, Samuele Renzi

Abstract readReview
In one paragraph

Review in Current oncology (Toronto, Ont.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

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

1 citing paper in PubMed.

  1. 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.

Jacob SilvermanMcGill Faculty of Medicine and Health Sciences, Montréal, QC H2V 4A9, Canada.ORCID 0009-0000-4314-9989
Sayanthen SathyakumarSunnybrook Research Institute, University of Toronto, Toronto, ON M4N 3M5, Canada.
Hallie ColtinDivision of Hematology-Oncology, CHU Sainte-Justine, Université de Montréal, Montréal, QC H3C 3A7, Canada.
Sebastien PerreaultDepartment of Neurology, Division of Child Neurology, CHU Sainte-Justine, Université de Montréal, Montréal, QC H3C 3A7, Canada.
Nada JabadoDepartment of Pediatrics, McGill University, Montreal, QC H4A 3J1, Canada.
Eric BouffetDivision of Pediatric Hematology-Oncology, Hospital for Sick Children, Toronto, ON M5G 1E8, Canada.ORCID 0000-0002-6832-6539
Samuele RenziDepartment of Pediatrics, Division of Hematology-Oncology, CHU de Québec, Université Laval, Québec City, QC G1V 4G2, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bevacizumab is often used off-label in pediatric neuro-oncology, and evidence for indications of bevacizumab use in pediatric neuro-oncology is often fragmented. Therefore, this review aims to provide an organized summary of efficacy across different types of tumors, highlight outcomes, and link findings to the underlying biology. Gaps in the literature were also identified to guide future research. We narratively synthesized various pediatric studies, and the following tumor categories were identified for discussion: low-grade glioma, high-grade glioma, diffuse intrinsic pontine glioma, schwannoma, medulloblastoma, radiation necrosis, and cerebral edema. Key outcomes considered included overall survival, event-free survival, progression-free survival, vision and/or hearing improvements, steroid use, quality of life, and toxicity. The greatest benefits were observed in cases such as recurrent medulloblastoma in combination with temozolomide and irinotecan, optic pathway glioma visual function, and diminished steroid use in radiation necrosis. Results were poorer in cases of newly diagnosed high-grade gliomas and diffuse intrinsic pontine gliomas. The medication was overall well tolerated, with adverse events like hypertension, proteinuria, and epistaxis often being manageable with surveillance. In consideration of the results, bevacizumab should be considered based on the tumor profile, and its outcome measured along functional endpoints, besides radiological evolution. Continued investigations into outcome measures, as well as combination with targeted treatments and optimizing therapy, will contribute to improving outcomes in this vulnerable population.

Indexed as

Angiogenesis InhibitorsAntineoplastic Agents, ImmunologicalBevacizumabBrain NeoplasmsChildGliomaHumansAngiogenesis InhibitorsAntineoplastic Agents, ImmunologicalBevacizumabangiogenesis inhibitorsbevacizumabpediatric neuro-oncology

Identifiers

PMID41149493
PMCPMC12564347

What OpenQuestion holds

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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.