Evidence map›Paper›PMID 31054099›Full record

Trial reportJournal of neuro-oncology2019

Contrast-enhancement in supratentorial low-grade gliomas: a classic prognostic factor in the molecular age.

Florian Castet, Enrique Alanya, Noemi Vidal, Cristina Izquierdo, Carlos Mesia, François Ducray, Miguel Gil-Gil, Jordi Bruna

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Journal of neuro-oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Characteristics of [European journal of nuclear medicine and molecular imaging · 2026
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  11. CombiningJournal of neuro-oncology · 2021
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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

8 authors.

Florian CastetMedical Oncology Department, Institut Català D'Oncologia L'Hospitalet, Barcelona, Spain.
Enrique AlanyaMedical Oncology and Radiotherapy Department, Edgardo Rebagliati Martins National Hospital - EsSalud, Lima, Peru.
Noemi VidalPathology Department, Hospital Universitari de Bellvitge, Barcelona, Spain.
Cristina IzquierdoUnit of Neuro-Oncology, Hospital Universitari de Bellvitge-Institut Català D'Oncologia L'Hospitalet, IDIBELL (Oncobell Program), Feixa Llarga s/n, 08907, Barcelona, Spain.
Carlos MesiaMedical Oncology Department, Institut Català D'Oncologia L'Hospitalet, Barcelona, Spain.
François DucrayGroupe Hospitalier Est, Service de Neuro-Oncologie, Hospices Civils de Lyon, Lyon, France.
Miguel Gil-GilMedical Oncology Department, Institut Català D'Oncologia L'Hospitalet, Barcelona, Spain.
Jordi BrunaUnit of Neuro-Oncology, Hospital Universitari de Bellvitge-Institut Català D'Oncologia L'Hospitalet, IDIBELL (Oncobell Program), Feixa Llarga s/n, 08907, Barcelona, Spain. 35078jbe@comb.cat.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundContrast enhancement (CE) is found in 10-60% of low-grade gliomas. Its prognostic significance is controversial, and its correlation with IDH mutations and 1p/19q codeletion is elusive. The aim of this study is to investigate whether CE is associated with molecular characteristics of low-grade gliomas and uncover its prognostic value. MATERIALS AND

methodsAll confirmed histological cases of low-grade gliomas diagnosed at our institution between years 2000-2016 were reviewed (n = 102). Spinal and brainstem localization, only-biopsied tumours with ring-like enhancement and incomplete medical records were excluded.

resultsMean age was 42 years ( ± 13.9 years), and 63.6% were male. The median follow-up time was 79.8 months. CE was present on 25% of preoperative MRI, and 25% of patients were considered high-risk according to Pignatti score. Most were astrocytomas (67%) and 87.2% were surgically removed. IDH mutation was found in 64.6% of tumour samples, and 18.8% had a 1p/19q codeletion. No subgroup differences were observed according to CE except for presurgical performance status and postoperative chemotherapy. IDH status and 1p/19q codeletion were evenly distributed. On univariate analysis, age, size > 6 cm, CE, extent of resection, Pignatti score, IDH mutation and 1p/19q codeletion were significantly associated to OS. On multivariate analysis, only CE and IDH status were independently associated to OS. CE remained a significant prognostic factor in IDH-mutant non-codeleted tumours when analysed by tumour subtype.

conclusionCE in low-grade gliomas provides prognostic information in IDH-mutant non-codeleted tumours, although its meaning remains uncertain in IDH-wildtype gliomas.

Indexed as

Chromosome DeletionContrast MediaMutationAdultBiomarkers, TumorChromosomes, Human, Pair 1Chromosomes, Human, Pair 19Combined Modality TherapyFemaleFollow-Up StudiesGliomaHumansImage EnhancementIsocitrate DehydrogenaseMagnetic Resonance ImagingMaleBiomarkers, TumorContrast MediaIDH1 protein, humanIDH2 protein, humanIsocitrate DehydrogenaseAstrocytomaContrast-enhancementIDHLow-grade gliomaPrognosis

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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.