Evidence map›Paper›PMID 41844910›Full record

ReviewJournal of neurology2026

Treatment-free remission in MS: long-term disease control with cladribine tablets.

Heinz Wiendl, Ralf Gold, Refik Pul, Michael Ernst, Markus C Kowarik, Juliane Klehmet, Ines Siglienti, Michael Hübschen, Torsten Wagner, Judith Knaup and 1 more

Abstract readReview
In one paragraph

Review in Journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

11 authors.

Heinz Wiendl *Department of Neurology and Neurophysiology, University Medical Center, Freiburg, Germany.ORCID http://orcid.org/0000-0003-4310-3432
Ralf Gold *Department of Neurology, St. Josef-Hospital Bochum, Ruhr University Bochum, Gudrunstr. 56, 44791, Bochum, Germany. ralf.gold@rub.de.ORCID http://orcid.org/0000-0002-7223-3052
Refik PulDepartment of Neurology and Center for Translational Neuro- and Behavioral Sciences, University Medicine Essen, Essen, Germany.ORCID http://orcid.org/0000-0002-8940-9317
Michael ErnstNeurology Practice Sinsheim, Sinsheim, Germany.
Markus C KowarikDepartment of Neurology & Stroke, and Hertie-Institute for Clinical Brain Research, Eberhard-Karls University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0003-1389-5539
Juliane KlehmetCenter for Multiple Sclerosis, Department of Neurology, Jüdisches Krankenhaus Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0002-8722-9785
Ines SiglientiDepartment of Neurology, St. Josef-Hospital Bochum, Ruhr University Bochum, Gudrunstr. 56, 44791, Bochum, Germany.
Michael HübschenMerck Healthcare Germany GmbH (an affiliate of Merck KGaA), Weiterstadt, Germany.
Torsten WagnerMerck Healthcare Germany GmbH (an affiliate of Merck KGaA), Weiterstadt, Germany.ORCID http://orcid.org/0009-0005-7479-4311
Judith KnaupMerck Healthcare Germany GmbH (an affiliate of Merck KGaA), Weiterstadt, Germany.ORCID http://orcid.org/0009-0006-5062-1093
Christoph KleinschnitzDepartment of Neurology and Center for Translational Neuro- and Behavioral Sciences, University Medicine Essen, Essen, Germany.ORCID http://orcid.org/0000-0002-1650-8875

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral cladribine, a highly effective pulsed selective immune reconstitution therapy (SIRT) for relapsing multiple sclerosis (RMS) is characterised by extended treatment-free periods following brief exposure to medication. Since approval in 2017, long-term real-world data have become available which provide insight into the management of patients treated with cladribine tablets beyond year 4. Most patients remained without additional therapy, which may hint at stable disease control. However, the absence of further treatment must not necessarily be interpreted as absence of any disease activity, as MRI data are often incomplete in watch-and-wait cohorts. The observed long-term remission is likely linked to the unique mode of action, which involves rapid repopulation of lymphocytes with different dynamics amongst subsets and sustained reduction of memory B cells. The recovery of the immune system and lymphocytes preserves long-term therapeutic options with existing or upcoming drugs. In cases of mild recurring disease activity, retreatment with cladribine tablets has been shown to be effective and tolerable within the known safety profile. Unrestricted long-term management options associated with cladribine tablets include a switch to other DMTs in cases of insufficient disease control. Overall, cladribine tablets show potential of a paradigmatic shift in MS management that may enable treatment-free remission over 6 years as an achievable treatment goal in a substantial proportion of RMS patients.

Indexed as

CladribineImmunosuppressive AgentsMultiple SclerosisMultiple Sclerosis, Relapsing-RemittingHumansRemission InductionTabletsCladribineImmunosuppressive AgentsTabletsCladribineImmune reconstitutionMultiple sclerosisRemissionTreatment-free

Identifiers

PMID41844910
PMCPMC12996015

What Socratic holds

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Registered trials

None linked

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.