Evidence map›Paper›PMID 41696492›Full record

ArticleNeuro-oncology advances

Beyond proof-of-concept: Validating robust automated diffuse lower-grade glioma segmentation for clinical applications in longitudinal follow-up.

Jeremy Deverdun, Guillaume Clain, Margaux Verdier, Hugues Duffau, Liesjet E H Van Dokkum, Nicolas Menjot de Champfleur, Justine Meriadec, Mathilde Carriere, Amelie Darlix, Emmanuelle Le Bars

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Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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

10 authors.

Jeremy DeverdunDepartment of Neuroradiology, Institute of Human Functional Imaging, Montpellier University Hospital.ORCID https://orcid.org/0000-0002-7083-2940
Guillaume ClainDepartment of Neuroradiology, Institute of Human Functional Imaging, Montpellier University Hospital.
Margaux VerdierDepartment of Neuroradiology, Institute of Human Functional Imaging, Montpellier University Hospital.
Hugues DuffauDepartment of Neurosurgery, Gui de Chauliac Hospital, Montpellier University Medical Center, Montpellier (H.D.); Team "Plasticity of Central Nervous System, Stem Cells and Glial Tumors", INSERM U1191, Institute of Functional Genomics, Montpellier (H.D.).ORCID https://orcid.org/0000-0002-6558-2342
Liesjet E H Van DokkumDepartment of Neuroradiology, Montpellier University Hospital.
Nicolas Menjot de ChampfleurDepartment of Neuroradiology, Montpellier University Hospital.
Justine MeriadecDepartment of Neuroradiology, Montpellier University Hospital.
Mathilde CarriereDepartment of Neuroradiology, Montpellier University Hospital.
Amelie DarlixDepartment of Medical Oncology, Institut Régional du Cancer de Montpellier, University of Montpellier, Montpellier (A.D.).ORCID https://orcid.org/0000-0003-1384-1709
Emmanuelle Le BarsDepartment of Neuroradiology, Institute of Human Functional Imaging, Montpellier University Hospital.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Monitoring diffuse lower-grade glioma (DLGG) evolution on MRI is challenging due to their infiltrative nature and post-surgical deformations. The RANO criteria recommend assessing the 2D tumor size, but volume analysis remains the gold standard for calculating growth rate. Manual tumor segmentation, however, is time-consuming, limiting its use in clinical practice. Automated segmentation tools like nnU-Net are promising but require clinical validation. Methods: We used 1971 MRI exams from 207 DLGG patients to train and validate an in house-developed nnU-Net al.orithm. The dataset included scans from various MRI systems, with 2D and 3D FLAIR and T1-weighted acquisitions, that were divided into derivation ( Results: The median nnU-Net DSC and IoU were 0.93 and 0.86, respectively. In the validation cohort, 64% of exams had excellent (≥0.9), 31% good ([0.7-0.9]), 3.5% unsatisfactory ([0.5-0.7]), and 1.5% poor DSC (<0.5). Higher DSC correlated with larger tumor volumes ( Conclusions: Our automated nnU-Net segmentation tool demonstrates high accuracy and potential for clinical integration, enhancing DLGG monitoring and management.

Indexed as

automated segmentationclinical MRIdiffuse lower-grade gliomalongitudinal follow-uptumor volume

Identifiers

PMID41696492
PMCPMC12901730

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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.