Evidence map›Paper›PMID 34114065›Full record

ArticleNeuroradiology2021

Perfusion imaging with arterial spin labeling (ASL)-MRI predicts malignant progression in low‑grade (WHO grade II) gliomas.

Christina M Flies, Tom J Snijders, Tom Van Seeters, Marion Smits, Filip Y F De Vos, Jeroen Hendrikse, Jan Willem Dankbaar

Open access · hybridAbstract read
In one paragraph

Article in Neuroradiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Observational
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Advanced MR Techniques for Preoperative Glioma Characterization: Part 1.Journal of magnetic resonance imaging : JMRI · 2023
    Review
  9. Review
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 at 3 institutions in 2 countries.

Christina M FliesDepartment of Neurology & Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-9160-4058
Tom J SnijdersDepartment of Neurology & Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, the Netherlands. T.J.Snijders@umcutrecht.nl.ORCID http://orcid.org/0000-0003-0857-081X
Tom Van SeetersDepartment of Radiology, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0001-8839-964X
Marion SmitsDepartment of Radiology and Nuclear Medicine, Erasmus MC, University Medical Centre Rotterdam, Rotterdam, the Netherlands.ORCID http://orcid.org/0000-0001-5563-2871
Filip Y F De VosDepartment of Medical Oncology, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-9082-5991
Jeroen HendrikseDepartment of Radiology, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0001-6384-6140
Jan Willem DankbaarDepartment of Radiology, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0003-4646-9587
University Medical Center Utrecht · NLHeidelberg University · DEErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePredicting malignant progression of grade II gliomas would allow for earlier initiation of treatment. The hypothesis for this single-centre, case-control study was that the perfusion signal on ASL-MRI predicts such malignant progression in the following 12 months.

methodsConsecutive patients with the following criteria were included: ≥ 18 years, grade II glioma (biopsied or resected) and an ASL-MRI 6-12 months prior to malignant progression (cases) or stable disease (controls). Malignant progression was defined either radiologically (new T1w-contrast enhancement) or histologically (neurosurgical tissue sampling). Three controls were matched with each case. Some patients served as their own control by using earlier imaging. The ASL-MRIs were reviewed by two neuroradiologists and classified as positive (hyper-intense or iso-intense compared to cortical grey matter) or negative (hypo-intense). In patients with epilepsy, a neurologist reviewed clinicoradiological data to exclude peri-ictal pseudoprogression. The statistical analysis included diagnostic test properties, a Cohen's Kappa interrater reliability coefficient and stratification for previous radiotherapy.

resultsEleven cases (median age = 48, IQR = 43-50 years) and 33 controls (43, 27-50 years) were included. Malignant progression appeared at 37 months (median, IQR = 17-44) after first surgery. Thirty ASL-MRIs were assessed as negative and 14 as positive. None of the MRIs showed signs of peri-ictal pseudoprogression. ASL significantly predicted subsequent malignant progression (sensitivity = 73%; specificity = 82%; OR = 12; 95%-CI = 2.4-59.1; p = 0.002). The interrater reliability coefficient was 0.65. In stratified analysis, ASL-MRI predicted malignant progression both in patients with previous radiotherapy and in those without (Mantel-Haenszel test, p = 0.003).

conclusionPerfusion imaging with ASL-MRI can predict malignant progression within 12 months in patients with grade II glioma.

Indexed as

Brain NeoplasmsGliomaCase-Control StudiesCerebrovascular CirculationContrast MediaHumansMagnetic Resonance ImagingMiddle AgedPerfusion ImagingReproducibility of ResultsSpin LabelsWorld Health OrganizationContrast MediaSpin LabelsArterial spin labelingLow-grade gliomaMalignant progressionPerfusion MRI

Identifiers

PMID34114065
PMCPMC8589747
OpenAlexW3170823054

What OpenQuestion holds

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LicenceCC BY
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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.