Evidence map›Paper›PMID 39917759›Full record

ArticleNeuro-oncology practice2025

Improved diagnostic accuracy for leptomeningeal dissemination in pediatric brain tumors using contrast-enhanced FLAIR imaging.

Berna Aygun, Asthik Biswas, Mohammed Blaaza, Jessica Cooper, Pritika Gaur, Jernej Avsenik, Harini R Rao, James Stegeman, Ulrike Löbel, Elwira Szychot and 3 more

Abstract read
In one paragraph

Article in Neuro-oncology practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 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

3 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Guideline
  2. Pooled it
  3. 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

13 authors.

Berna AygunDepartment of Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.ORCID https://orcid.org/0009-0005-0319-1695
Asthik BiswasDepartment of Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Mohammed BlaazaDepartment of Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Jessica CooperDepartment of Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Pritika GaurDepartment of Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Jernej AvsenikClinical Institute of Radiology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Harini R RaoDepartment of Haematology-Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
James StegemanMonash Imaging, Monash Children's Hospital, Monash Health, Melbourne, Australia.
Ulrike LöbelDepartment of Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Elwira SzychotDepartment of Pediatrics, Pediatric Oncology and Immunology, Pomeranian Medical University, Szczecin, Poland.
Felice D'ArcoDepartment of Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Sniya SudhakarDepartment of Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Kshitij MankadDepartment of Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Central nervous system cancers are a leading cause of childhood cancer-related mortality. Accurate staging and assessment of leptomeningeal spread, particularly in aggressive neoplasms such as embryonal tumors, is crucial for treatment planning and prognosis. Conventional diagnostic methods, relying on magnetic resonance imaging (MRI) and cerebrospinal fluid (CSF) cytology, have limitations, including high false-negative rates and sensitivity issues. In this retrospective study, we aim to compare the diagnostic sensitivity of contrast-enhanced T2-weighted fluid-attenuated inversion recovery (CE-T2W-FLAIR) and 2D and 3D contrast-enhanced T1-weighted imaging (CE-T1WI) for detecting leptomeningeal disease. Methods: We retrospectively reviewed 1372 MRI brain studies of 297 patients aged 1-19 years. We included only those MRI examinations adhering to our neuro-oncology protocol while excluding incomplete or suboptimal studies. A control group without leptomeningeal disease was matched for disease and age. Three groups of 2 neuroradiologists each, blinded to case status, reviewed the images using various sequences. The results were compared using the McNemar test and chi-squared test for Results: The sensitivity of CE-T2W-FLAIR sequence was significantly higher compared with that of CE-T1WI ( Conclusions: The inclusion of CE-T2W-FLAIR in the MRI protocol improves sensitivity and specificity in diagnosing leptomeningeal spread in pediatric brain tumors.

Indexed as

contrast-enhanced T1WIcontrast-enhanced T2W-FLAIRleptomeningeal disseminationneuro-oncologypediatric brain tumors

Identifiers

PMID39917759
PMCPMC11798603

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.