Evidence map›Paper›PMID 42168373›Full record

ArticleScientific reports2026

Performances of experts and automated methods on new multiple sclerosis lesions detection: insights from the MSSeg2 challenge.

Arthur Masson, Benoit Combès, Anne Kerbrat, François-Daniel Ardellier, Sylvain Rabaste, Pauline Cloarec, Quentin Wdowik, Gilles Edan, Frédéric Cervenansky, Romain Casey and 6 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Arthur MassonInria, CNRS, Inserm. IRISA UMR 6074, Empenn ERL U1228, University of Rennes, 35000, Rennes, France.
Benoit CombèsInria, CNRS, Inserm. IRISA UMR 6074, Empenn ERL U1228, University of Rennes, 35000, Rennes, France. benoit.combes@inria.fr.
Anne KerbratInria, CNRS, Inserm. IRISA UMR 6074, Empenn ERL U1228, University of Rennes, 35000, Rennes, France.
François-Daniel ArdellierService d'Imagerie 2 - Hôpital de Hautepierre, Hôpitaux Universitaire de Strasbourg, 67200, Strasbourg, France.
Sylvain RabasteCHU Lyon, 69000, Lyon, France.
Pauline CloarecCHU Rennes, 35000, Rennes, France.
Quentin WdowikCHU Lyon, 69000, Lyon, France.
Gilles EdanInria, CNRS, Inserm. IRISA UMR 6074, Empenn ERL U1228, University of Rennes, 35000, Rennes, France.
Frédéric CervenanskyINSA-Lyon, Universite Claude Bernard Lyon 1, CNRS, Inserm, CREATIS UMR 5220, U1294, 69XXX, LYON, France.
Romain CaseyUniversité Claude Bernard Lyon 1, Hospices Civils de Lyon, Fondation EDMUS, OFSEP, Centre de Recherche en Neurosciences de Lyon, University of Lyon, 69000, Lyon, France.
Sorina Camarasu-PopINSA-Lyon, Universite Claude Bernard Lyon 1, CNRS, Inserm, CREATIS UMR 5220, U1294, 69XXX, LYON, France.
Axel BonnetINSA-Lyon, Universite Claude Bernard Lyon 1, CNRS, Inserm, CREATIS UMR 5220, U1294, 69XXX, LYON, France.
Michael KainInria, CNRS, Inserm. IRISA UMR 6074, Empenn ERL U1228, University of Rennes, 35000, Rennes, France.
Michel DojatInserm U1216, Grenoble Institut des Neurosciences, Université Grenoble Alpes, 38000, Grenoble, France.
Francois CottonDepartment of Neuroradiology, CHU Lyon, 69000, Lyon, France.
Olivier CommowickInria, CNRS, Inserm. IRISA UMR 6074, Empenn ERL U1228, University of Rennes, 35000, Rennes, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The assessment of new Multiple Sclerosis (MS) lesions is a time-consuming and difficult task that may lead to an underestimation of patient disease activity. Efficient methods to detect new T2/FLAIR lesions are therefore critical to assist clinicians in this process. In this context, we proposed and organized in 2021 the MSSeg2 challenge aiming at comparing methods segmenting new MS lesions. For this purpose, we built a high-quality dataset of 100 pairs of FLAIR MRI with precise delineation of new MS lesions with a size superior to 3 mm[Formula: see text]. From these 100 pairs of MS patient images from various scanners and French clinical centers, 40 were shared to the challengers before they submitted their methods. 30 methods from 24 international teams were submitted and evaluated on the FLI-IAM dedicated platform on the 60 remaining images. Overall, we observed that even at lesion scale, expert annotations were variable (40% of lesions were annotated by two or fewer experts out of the four). The best expert exhibited a mean F1 score of 0.679 (SD = 0.345) while the best method exhibited a mean F1 score of 0.698 (SD = 0.295) on the 35 patients with new lesions. Moreover, we did not observe evidence of differences between the top-ranked methods and the best expert performances as evaluated by the F1 score (9 methods exhibited no clear evidence against no difference of mean F1). Similarly, we did not observe evidence of difference in performances between the top-ranked methods and the best expert in classifying patients into a 3 categories clinically relevant scale (0 lesion, 1 or 2 lesions and >2 lesions; 21 methods exhibited no clear evidence against no difference of performances with a best classification accuracy of 85 % for both the best expert and the best method). While results from current automated methods still remain perfectible, our results highlight their potential usefulness in detecting new FLAIR MS lesions.

Indexed as

Image Interpretation, Computer-AssistedImage Processing, Computer-AssistedMagnetic Resonance ImagingMultiple SclerosisFemaleHumans

Identifiers

PMID42168373
PMCPMC13402319

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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.