Evidence map›Paper›PMID 40016316›Full record

ArticleEuropean radiology2025

How useful is contrast-enhanced MRI in the long-term surveillance of glioma? A multicentre retrospective longitudinal cohort study.

Marcus Cakmak, Sepehr Mohammadian, Vera C W Keil, Joost W Schouten, Philip C de Witt Hamer, Thijs van der Vaart, Rutger K Balvers, Ivar J H G Wamelink, Frederik Barkhof, Martin van den Bent and 2 more

Abstract readMulticenter Study
In one paragraph

Article in European radiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Dynamic glucose-enhanced MRI in brain tumors.Magma (New York, N.Y.) · 2026
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Marcus Cakmak *Department of Radiology and Nuclear Medicine, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Sepehr Mohammadian *Department of Radiology and Nuclear Medicine, University Medical Centre Rotterdam, Rotterdam, The Netherlands.
Vera C W KeilDepartment of Radiology and Nuclear Medicine, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Joost W SchoutenDepartment of Neurosurgery, University Medical Centre Rotterdam, Rotterdam, The Netherlands.
Philip C de Witt HamerBrain Tumour Centre, Cancer Centre Amsterdam, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Thijs van der VaartDepartment of Neurology, University Medical Centre Rotterdam, Rotterdam, The Netherlands.
Rutger K BalversDepartment of Neurosurgery, University Medical Centre Rotterdam, Rotterdam, The Netherlands.
Ivar J H G WamelinkDepartment of Radiology and Nuclear Medicine, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Frederik BarkhofDepartment of Radiology and Nuclear Medicine, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Martin van den BentBrain Tumour Centre, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Mark Vries *Department of Radiology and Nuclear Medicine, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Marion Smits *Department of Radiology and Nuclear Medicine, University Medical Centre Rotterdam, Rotterdam, The Netherlands. marion.smits@erasmusmc.nl.ORCID http://orcid.org/0000-0001-5563-2871

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo examine whether MRI with routine gadolinium-based contrast agent (GBCA) administration in the long-term surveillance of adult-type diffuse glioma identifies tumour progression earlier than T2-weighted (T2w) and/or T2w fluid-attenuated inversion recovery (FLAIR) MRI only. MATERIALS AND

methodsIn this longitudinal retrospective multicentre cohort study patients with histopathologically confirmed adult-type diffuse glioma and at least two years survival after diagnosis in 2009-2010 were included. Progression was determined by the treating physician or during the multidisciplinary team meeting and defined as the moment a change in treatment or follow-up was required. The primary outcome was the proportion of patients that showed an increase of abnormalities on both contrast-enhanced T1-weighted (CET1w) and T2w/T2w-FLAIR at the time of progression. Chi-square testing was performed to analyse the relationship between the detection of progression on both scan sequences, with calculating the Phi coefficient to determine the degree of association.

resultsOne hundred eight consecutive patients were included (58 male; 53 grade 2, 21 grade 3, 34 grade 4). Progression was present in 82 patients and was determined on both CET1w and T2w/T2w-FLAIR images in 59 patients (72.0%). In 20 patients (24.4%), progression was determined based solely on T2w/T2w-FLAIR abnormalities. Only three patients showed progression exclusively on CET1w (3.7%). There was a strong positive significant relationship between the detection of progression on both scan types (p < 0.001; Phi = 0.467).

conclusionAn increase in CET1w abnormalities was generally accompanied by an increase in T2w/T2w-FLAIR abnormalities, raising the question of whether routine administration of GBCA is always necessary for long-term survivors of glioma. KEY POINTS: Question Long-term survivors with glioma undergo many contrast-enhanced MRI scans, which involve a patient, financial, and environmental burden. Findings In almost all patients, an increase in T2w/T2w-FLAIR abnormalities was present at the time of tumour progression, mostly but not always accompanying contrast-enhancing findings. Clinical relevance T2w/T2-FLAIR MRI seems to detect glioma progression in long-term surviving patients similar to contrast-enhanced T1w MRI, raising the question of whether the routine administration of GBCA is necessary and justified in patients under long-term surveillance of glioma.

Indexed as

Brain NeoplasmsContrast MediaGliomaMagnetic Resonance ImagingAdultAgedDisease ProgressionFemaleGadoliniumHumansLongitudinal StudiesMaleMiddle AgedRetrospective StudiesContrast MediaGadoliniumContrast mediaDisease progressionGliomaMagnetic resonance imaging

Identifiers

PMID40016316
PMCPMC12165967

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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.