Evidence map›Paper›PMID 41719500›Full record

ArticleNeurology(R) neuroimmunology & neuroinflammation2026

Outcome Predictors in Progressive Multifocal Leukoencephalopathy Associated With Multiple Sclerosis Treatments: A Multicenter Cohort Study.

Julie Céline Blant, Nicola De Rossi, Ralf Gold, Aude Maurousset, Markus Kraemer, Lucía Romero-Pinel, Tatsuro Misu, Jean-Christophe Ouallet, Maud Pallix Guyot, Simonetta Gerevini and 15 more

Abstract readMulticenter Study
In one paragraph

Article in Neurology(R) neuroimmunology & neuroinflammation, 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

25 authors.

Julie Céline BlantService of Neurology, Department of Clinical Neurosciences, Lausanne University Hospital (Centre Hospitalier Universitaire Vaudois) and University of Lausanne, Switzerland.ORCID 0009-0005-8840-2446
Nicola De RossiRegional Multiple Sclerosis Center, ASST-Spedali Civili dii Brescia, Montichiari, Italy.ORCID 0000-0002-3509-4882
Ralf GoldDepartment of Neurology St. Josef-Hospital, Ruhr University Bochum, Germany.ORCID 0000-0002-7223-3052
Aude MauroussetCentre hospitalier régional universitaire de Tours, Hôpital Bretonneau, Service de neurologie, France.ORCID 0000-0002-3916-4606
Markus KraemerDepartment of Neurology, Alfried Krupp von Bohlen und Halbach Hospital, Essen, Germany.ORCID 0000-0002-5667-3621
Lucía Romero-PinelNeurology Department, Multiple Sclerosis Unit, Hospital Universitari de Bellvitge, IDIBELL, Barcelona, Spain.ORCID 0000-0001-8054-0565
Tatsuro MisuDepartment of Neurology, Tohoku University Hospital, Japan.ORCID 0000-0002-7311-2578
Jean-Christophe OualletService de Neurologie, Pôle des Neurosciences Cliniques, CHU de Bordeaux Pellegrin Tripode, France.ORCID 0000-0003-3231-6416
Maud Pallix GuyotService de Neurologie et Unité Neurovasculaire, Centre Hospitalier Régional d'Orléans, France.ORCID 0009-0008-3880-3809
Simonetta GereviniUnit of Neuroradiology, Papa Giovanni XXIII Hospital, Bergamo, Italy.ORCID 0000-0002-2374-194X
Christos BakirtzisMultiple Sclerosis Center, Second Department of Neurology, Aristotle University of Thessaloniki, Greece.ORCID 0000-0002-4737-3707
Raquel Piñar MoralesServicio de Neurología, Hospital Universitario Clínico San Cecilio, Granada, Spain.ORCID 0000-0003-3490-4932
Benjamin VladDepartment of Neurology, University Hospital Zürich and University of Zürich, Switzerland.ORCID 0009-0002-8830-0173
Panajotis KarypidisNeurologic Clinic and Policlinic and Research Center for Clinical Neuroimmunology and Neuroscience, Departments of Medicine, Biomedicine, and Clinical Research, University Hospital Basel, University of Basel, Switzerland.ORCID 0009-0007-9766-6923
Xavier MoissetService de Neurologie, Université Clermont Auvergne, CHU de Clermont-Ferrand, Inserm, Neuro-Dol, Clermont-Ferrand, France.ORCID 0000-0002-8799-0750
Tobias J DerfussNeurologic Clinic and Policlinic and Research Center for Clinical Neuroimmunology and Neuroscience, Departments of Medicine, Biomedicine, and Clinical Research, University Hospital Basel, University of Basel, Switzerland.ORCID 0000-0001-8656-4250
Ilijas JelcicDepartment of Neurology, University Hospital Zürich and University of Zürich, Switzerland.ORCID 0000-0003-3090-7319
Guillaume Martin-BlondelUniversity Hospital of Toulouse, Infectious and Tropical Diseases Unit, France.ORCID 0000-0002-8363-7028
Ilya AyzenbergDepartment of Neurology St. Josef-Hospital, Ruhr University Bochum, Germany.ORCID 0009-0007-9491-2180
Corey McGrawDepartment of Neurology, State University of New York Upstate Medical University, Syracuse.ORCID 0009-0007-6158-8484
David Axel LaplaudCHU Nantes, Service de Neurologie, CRC-SEP, Nantes Université, INSERM, CIC 1413, Center for Research in Transplantation and Translational Immunology, UMR, France.ORCID 0000-0001-6113-6938
Christine Lebrun-FrenayNeurology, UR2CA_URRIS, Centre Hospitalier Universitaire Pasteur2, Université Nice Côte d'Azur, France; and.ORCID 0000-0002-3713-2416
Renaud A Du PasquierService of Neurology, Department of Clinical Neurosciences, Lausanne University Hospital (Centre Hospitalier Universitaire Vaudois) and University of Lausanne, Switzerland.ORCID 0000-0002-2786-3434
Raphael Bernard-ValnetService of Neurology, Department of Clinical Neurosciences, Lausanne University Hospital (Centre Hospitalier Universitaire Vaudois) and University of Lausanne, Switzerland.ORCID 0000-0001-7447-344X
CORPUS and Italian PML study groups

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesJC virus (JCV) reactivation causing progressive multifocal leukoencephalopathy (PML) is a complication in patients with multiple sclerosis (MS) treated with disease-modifying therapies (DMTs). Although natalizumab (NTZ) is most frequently involved, PML also occurs less commonly with sphingosine-1-phosphate receptor modulators (S1P-RM), dimethyl fumarate (DMF), and ocrelizumab. This study aimed to identify factors predicting worse outcomes, focusing on the influence of PML-immune reconstitution inflammatory syndrome (PML-IRIS), plasma exchange (PlEx), corticosteroids, and DMT reintroduction.

methodsThis retrospective multicenter cohort study analyzed patients with MS who had JCV-associated pathology (PML or granule cell neuronopathy) from 42 centers (2009-2022). The primary outcome was disability at 12 months, measured by the modified Rankin Scale (mRS). Multivariable analyses identified predictors of poor outcomes, PML-IRIS development, and recurrent MS activity.

resultsOf 96 identified patients, 94 were analyzed. Most cases occurred under NTZ (77%), followed by S1P-RM (22%) and DMF (1%). Twelve-month survival was 91.5%, with a median mRS of 3 [IQR: 2-4]. Multivariable analysis showed that higher pre-PML disability (OR: 1.95 [95% CI 1.46-2.60], DISCUSSION: This study provides valuable insights into the management of iatrogenic PML in patients with MS. The findings may guide clinicians in making informed decisions, particularly regarding the use of PlEx, corticosteroids, and the management of PML-IRIS.

Indexed as

Immune Reconstitution Inflammatory SyndromeImmunologic FactorsLeukoencephalopathy, Progressive MultifocalMultiple SclerosisOutcome Assessment, Health CareAdultCohort StudiesFemaleHumansJC VirusMaleMiddle AgedNatalizumabPlasma ExchangeRetrospective StudiesImmunologic FactorsNatalizumab

Identifiers

PMID41719500
PMCPMC12931519

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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.