Evidence map›Paper›PMID 42596034›Full record

ArticleAnnals of clinical and translational neurology2026

Anti-CD20 Discontinuation Versus Continuation in People Aged Over 50 With Non-Active Multiple Sclerosis.

Alexia Moukhine, Fabien Rollot, Romain Casey, Nicolas Collongues, Sandra Vukusic, Guillaume Mathey, Anne Laure Dubessy, Jonathan Ciron, Jérôme De Seze, Aurélie Ruet and 31 more

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

41 authors.

Alexia MoukhineDepartment of Neurology, University Hospital of Rennes, Rennes, France.
Fabien RollotUniversité de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.ORCID https://orcid.org/0000-0002-5752-2331
Romain CaseyUniversité de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
Nicolas CollonguesDepartment of Neurology and Clinical Investigation Center, CIC 1434, INSERM 1434, CHU de Strasbourg, Strasbourg, France.
Sandra VukusicUniversité de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
Guillaume MatheyDepartment of Neurology, Nancy University Hospital, Nancy, France.
Anne Laure DubessyDépartement de Neurologie, Hôpital Pitié-Salpêtrière, APHP, Paris, France.
Jonathan CironDepartment of Neurology, CRC-SEP, CHU de Toulouse, Toulouse, France.
Jérôme De SezeDepartment of Neurology and Clinical Investigation Center, CIC 1434, INSERM 1434, CHU de Strasbourg, Strasbourg, France.
Aurélie RuetDepartment of Neurology, University Hospital of Bordeaux, Bordeaux, France.
Pierre LabaugeMS Unit, CHU de Montpellier, Montpellier Cedex 5, France.
Arnaud KwiatkowskiDepartment of Neurology, Groupement des Hôpitaux de l'Institut Catholique de Lille, Hôpital Saint Vincent de Paul, Lille, France.
Hélène ZephirUniversité de Lille, Inserm U1172, CRC-SEP de Lille, CHU de Lille, Lille, France.
Caroline PapeixDepartment of Neurology, Foundation Adolphe de Rothschild Hospital, Université Paris-Cité, Paris, France.
Gilles DeferDepartment of Neurology, CHU de Caen, MS Expert Centre, Avenue de la Côte-de-Nacre, Normandy University, Caen, France.
Christine Lebrun-FrenayNeurology, UR2CA_URRIS, Centre Hospitalier Universitaire Pasteur2, Université Nice Côte d'Azur, Nice, France.ORCID https://orcid.org/0000-0002-3713-2416
David Axel LaplaudNantes Université, CHU Nantes, INSERM, Center for Research in Transplantation and Translational Immunology, UMR 1064, CIC INSERM 1413, CRC-SEP Pays de la Loire, Service de Neurologie, Nantes, France.
Eric BergerService de Neurologie, CHU de Besançon, Besançon, France.
Eric ThouvenotCHU Nimes, Service de Neurologie, University of Montpellier, Nimes, France.
Jean PelletierAix Marseille University, APHM, Hôpital de la Timone, Pôle de Neurosciences Cliniques, Service de Neurologie, Marseille, France.
Abdullatif Al KhedrDepartment of Neurology, CHU d'Amiens, Amiens, France.
Olivier CasezDepartment of Neurology, CHU Grenoble Alpes, Neurology MS Clinic Grenoble, Grenoble Alpes University Hospital, Grenoble, France.
Bertrand BourreT-RAIG, TIMC-IMAG, Grenoble Alpes University, Grenoble, France.
Abir WahabDepartment of Neurology, APHP, Hôpital Henri Mondor, Créteil, France.
Laurent MagyDepartment of Neurology, CHU de Limoges, Hôpital Dupuytren, Limoges, France.
Jean-Philippe CamdessanchéDepartment of Neurology, CHU de Saint-Étienne, Hôpital Nord, Saint-Étienne, France.
Ines DoghriDepartment of Neurology, CHU de Tours, Hôpital Bretonneau, CRC SEP, Tours, France.
Solène MoulinDepartment of Neurology, CHU de Reims, CRC-SEP, Reims Cedex, France.
Mariana Sarov RivièreDepartment of Neurology, APHP, Hôpital Kremlin Bicêtre, Le Kremlin Bicêtre, France.
Karolina HankiewiczDepartment of Neurology, Hôpital Pierre Delafontaine, Centre Hospitalier de Saint-Denis, Saint-Denis, France.
Amélie Dos SantosDepartment of Neurology et Centre d'Investigation Clinique, CIC INSERM 1402, CHU La Milétrie, Hôpital Jean Bernard, Poitiers, France.ORCID https://orcid.org/0000-0002-9744-3873
Corinne PottierDepartment of Neurology, Hôpital NOVO, Site Pontoise, Pontoise, France.
Eric ManchonDepartment of Neurology, CH de Gonesse, Gonesse, France.
Jennifer AboabCentre Hospitalier National d'Ophtalmologie des Quinze-Vingts, Paris, France.
Maia TchikviladzeDepartment of Neurology, Hôpital Foch, Suresnes, France.
Thomas DavidDepartment of Neurology, CHU de la Martinique, Fort-de-France, France.ORCID https://orcid.org/0009-0005-0133-3274
Gilles EdanDepartment of Neurology, University Hospital of Rennes, Rennes, France.
Emmanuelle Le PageDepartment of Neurology, University Hospital of Rennes, Rennes, France.
Laure MichelDepartment of Neurology, University Hospital of Rennes, Rennes, France.
Anne KerbratDepartment of Neurology, University Hospital of Rennes, Rennes, France.ORCID https://orcid.org/0000-0002-4530-3553
OFSEP Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine whether discontinuing anti-CD20 therapy in people with relapsing-onset MS aged over 50 is associated with an increased risk of relapse, inflammatory activity, confirmed disability accrual, and serious infection compared with continuing therapy.

methodsThis observational, multicenter, retrospective cohort study included 2283 patients from the French MS registry aged > 50, who had received at least two cycles of anti-CD20 and had experienced no relapses or MRI activity for at least one year prior to inclusion. Patients were classified as discontinuing or continuing therapy and 1:1 matched using a time-dependent propensity score. Outcomes were time to first relapse, inflammatory activity (relapse and/or MRI activity), confirmed disability accrual, and serious infection.

resultsAmong 1900 patients continuing therapy and 383 discontinuing, 224 in each group were matched (mean age = 57.7 ± 5.9 years; mean EDSS = 5.4 ± 1.7; median follow-up after matching = 34.8 [21.6-50.4] months). There were no significant differences between groups in time to first relapse (HR = 0.6, 95% CI 0.3-1.3, p = 0.2), inflammatory activity (HR = 0.9, 95% CI 0.5-1.4, p = 0.6), confirmed disability accrual (HR = 1.2, 95% CI 0.9-1.7, p = 0.2), and serious infections (HR = 1.0, 95% CI 0.6-1.8, p = 0.9).

interpretationThis retrospective study found no evidence of differences between stopping and continuing anti-CD20 therapy regarding relapse, inflammatory activity, disability accrual, or serious infections in older patients with long-standing non-active MS over a median 2.9-year follow-up.

Indexed as

anti‐CD20discontinuationmultiple sclerosis

Identifiers

PMID42596034
PMCPMC13473194

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