Evidence map›Paper›PMID 32765892›Full record

ArticleNeuro-oncology practice2020

Bevacizumab for pediatric radiation necrosis.

Lorena V Baroni, Daniel Alderete, Palma Solano-Paez, Carlos Rugilo, Candela Freytes, Suzanne Laughlin, Adriana Fonseca, Ute Bartels, Uri Tabori, Eric Bouffet and 10 more

Open access · greenAbstract read
In one paragraph

Article in Neuro-oncology practice, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Bevacizumab in Pediatric Neuro-Oncology.Current oncology (Toronto, Ont.) · 2025
    Review
  4. Approaches to Reduce Toxicity in Pediatric Brain Tumors.Current oncology (Toronto, Ont.) · 2025
    Review
  5. Palliative care for children with central nervous system tumors: results of a Spanish multicenter study.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. 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

20 authors at 8 institutions in 5 countries.

Lorena V BaroniDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.
Daniel AldereteDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.
Palma Solano-PaezService of Pediatric Oncology, Hospital Infantil Virgen del Rocío, Seville, Spain.
Carlos RugiloService of Diagnostic Imaging, Hospital JP Garrahan, Buenos Aires, Argentina.
Candela FreytesService of Hematology/Oncology, Hospital JP Garrahan, Buenos Aires, Argentina.
Suzanne LaughlinDepartment of Diagnostic Imaging, Hospital for Sick Children, Toronto, ON, Canada.
Adriana FonsecaDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.
Ute BartelsDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.
Uri TaboriDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.
Eric BouffetDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.
Annie HuangDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.
Normand LaperriereRadiation Medicine Program, Princess Margaret Cancer Centre, Toronto, ON, Canada.
Derek S TsangRadiation Medicine Program, Princess Margaret Cancer Centre, Toronto, ON, Canada.
David SumerauerDepartment of Paediatric Haematology and Oncology, Second Medical School, Charles University and University Hospital Motol, Prague, Czech Republic.
Martin KynclDepartment of Radiology, University Hospital Motol, Second Faculty of Medicine, Charles University, Prague, Czech Republic.
Barbora OndrováProton Therapy Center Czech, Prague, Czech Republic.
Vajiranee S MalalasekeraChildren's Cancer Centre, Royal Children's Hospital, Melbourne, Australia.
Jordan R HansfordChildren's Cancer Centre, Royal Children's Hospital, Melbourne, Australia.
Michal ZápotockýDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.
Vijay RamaswamyDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.ORCID 0000-0002-6557-895X
Hospital for Sick Children · CAGarrahan Hospital · ARUniversity of Toronto · CACharles University · CZPrincess Margaret Cancer Centre · CARoyal Children's Hospital · AUHospital Universitario Virgen del Rocío · ESProton Therapy Centre · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRadiation necrosis is a frequent complication occurring after the treatment of pediatric brain tumors; however, treatment options remain a challenge. Bevacizumab is an anti-VEGF monoclonal antibody that has been shown in small adult cohorts to confer a benefit, specifically a reduction in steroid usage, but its use in children has not been well described.

methodsWe describe our experience with bevacizumab use for symptomatic radiation necrosis at 5 institutions including patients treated after both initial irradiation and reirradiation.

resultsWe identified 26 patients treated with bevacizumab for symptomatic radiation necrosis, with a wide range of underlying diagnoses. The average age at diagnosis of radiation necrosis was 10.7 years, with a median time between the last dose of radiation and the presentation of radiation necrosis of 3.8 months (range, 0.6-110 months). Overall, we observed that 13 of 26 patients (50%) had an objective clinical improvement, with only 1 patient suffering from significant hypertension. Radiological improvement, defined as reduced T2/fluid-attenuated inversion recovery signal and mass effect, was observed in 50% of patients; however, this did not completely overlap with clinical response. Both early and late radiation necrosis responded equally well to bevacizumab therapy. Overall, bevacizumab was very well tolerated, permitting a reduction of corticosteroid dose and/or duration in the majority of patients.

conclusionsBevacizumab appears to be effective and well-tolerated in children as treatment for symptomatic radiation necrosis and warrants more robust study in the context of controlled clinical trials.

Indexed as

bevacizumabdexamethasonepediatric brain tumorsradiation | radiation necrosis

Identifiers

PMID32765892
PMCPMC7393279
OpenAlexW3002085893

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.