Evidence mapPaperPMID 41344938Full record

ArticleNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2026

Switching from anti-CD20 therapies to cladribine and vice versa - Analysis of a German relapsing multiple sclerosis cohort.

Franz Felix Konen, Steffen Pfeuffer, Konstantin Fritz Jendretzky, Klaus Gehring, Birte Elias-Hamp, Kurt-Wolfram Sühs, Stephan Halle, Korbinian Brand, Ralf Lichtinghagen, Eline Willemse and 6 more

Abstract readMulticenter Study
In one paragraph

Article in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2026. 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
  2. Review
  3. Switching high efficacy therapies in Multiple Sclerosis: Does real world experience support such a strategy?Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    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.

Franz Felix KonenDepartment of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany. Electronic address: konen.felix@mh-hannover.de.
Steffen PfeufferDepartment of Neurology, University Hospital of Giessen and Marburg, Justus-Liebig-University-Giessen, Klinikstr. 33, 35392 Giessen, Germany. Electronic address: steffen.pfeuffer@neuro.med.uni-giessen.de.
Konstantin Fritz JendretzkyDepartment of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany. Electronic address: jendretzky.konstantin@mh-hannover.de.
Klaus GehringNeurozentrum am Klosterforst, Hanseaten-Platz 1, 25524 Itzehoe, Germany. Electronic address: gehring@neurologie-itzehoe.de.
Birte Elias-HampPraxis Dr. Elias-Hamp, Bengelsdorfstr. 5, 22179 Hamburg, Germany. Electronic address: info@neuropraxis-elias.de.
Kurt-Wolfram SühsDepartment of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany. Electronic address: suehs.kurt-wolfram@mh-hannover.de.
Stephan HalleInstitute of Clinical Chemistry and Laboratory Medicine, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany; Institute of Immunology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany. Electronic address: halle.stephan@mh-hannover.de.
Korbinian BrandInstitute of Clinical Chemistry and Laboratory Medicine, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany. Electronic address: brand.korbinian@mh-hannover.de.
Ralf LichtinghagenInstitute of Clinical Chemistry and Laboratory Medicine, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany. Electronic address: lichtinghagen.ralf@mh-hannover.de.
Eline WillemseMultiple Sclerosis Centre and Research Center for Clinical Neuroimmunology and Neuroscience (RC2NB), Neurology, Departments of Biomedicine and Clinical Research, University Hospital and University of Basel, Basel, Switzerland; Department of Neurology, University Hospital and University of Basel, Spitalstrasse 2, CH-4031 Basel, Switzerland. Electronic address: eline.willemse@usb.ch.
Marc PawlitzkiDepartment of Neurology, Medical Faculty, Heinrich-Heine-University Düsseldorf, Duesseldorf, Germany. Electronic address: MarcGuenter.Pawlitzki@med.uni-duesseldorf.de.
Jens KuhleMultiple Sclerosis Centre and Research Center for Clinical Neuroimmunology and Neuroscience (RC2NB), Neurology, Departments of Biomedicine and Clinical Research, University Hospital and University of Basel, Basel, Switzerland; Department of Neurology, University Hospital and University of Basel, Spitalstrasse 2, CH-4031 Basel, Switzerland. Electronic address: jens.kuhle@usb.ch.
Sven G MeuthDepartment of Neurology, Medical Faculty, Heinrich-Heine-University Düsseldorf, Duesseldorf, Germany. Electronic address: meuth@uni-duesseldorf.de.
Christoph KleinschnitzUniversity Medicine Essen, Neurology, Essen, Germany; Center for Translational Neuro- and Behavioral Sciences, University Medicine Essen, Neurology, Essen, Germany. Electronic address: Christoph.Kleinschnitz@uk-essen.de.
Refik PulUniversity Medicine Essen, Neurology, Essen, Germany; Center for Translational Neuro- and Behavioral Sciences, University Medicine Essen, Neurology, Essen, Germany. Electronic address: Refik.Pul@uk-essen.de.
Thomas SkripuletzDepartment of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany. Electronic address: skripuletz.thomas@mh-hannover.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-CD20 antibodies and cladribine are established therapies for active relapsing multiple sclerosis (RMS). Increasing evidence suggests that switching between these therapies may be beneficial in patients with ongoing disease activity under current treatment. In this multicenter retrospective study across six German MS centres, a total of 90 patients with active RMS were considered for inclusion, of whom 71 patients were switched either from anti-CD20 antibodies to cladribine (n ​= ​31) or from cladribine to anti-CD20 antibodies (n ​= ​40), with a minimum follow-up of 12 months. At treatment initiation, patients switching from anti-CD20 antibodies were older, had a longer disease duration, and a higher disability score compared to those switching from cladribine (p ​= ​0.0040, p ​= ​0.0447, p ​= ​0.0028, respectively). The primary reason for switching was disease activity. Following the switch, the proportion of patients with relapsing disease activity was markedly reduced (from 55 ​% to 16 ​% for anti-CD20 to cladribine, and from 83 ​% to 25 ​% for cladribine to anti-CD20). Clinical outcomes improved, while serum biomarkers such as neurofilament light chain and glial fibrillary acidic protein remained stable over six months. Notably, the prevalence of hypogammaglobulinemia decreased after switching from anti-CD20 therapies to cladribine. These results indicate that patients with active RMS can achieve clinical stabilization after switching therapies in either direction, underscoring the complementary mechanisms of action and the safety of such an approach in real-world practice.

Indexed as

Antigens, CD20CladribineDrug SubstitutionImmunosuppressive AgentsMultiple Sclerosis, Relapsing-RemittingAdultCohort StudiesFemaleFollow-Up StudiesGermanyHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAntigens, CD20CladribineImmunosuppressive AgentsActive multiple sclerosisAnti-CD20-TherapyCladribineSwitch

Identifiers

PMID41344938
PMCPMC12976515

What Socratic holds

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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 Socratic graph.