Evidence map›Paper›PMID 42911400›Full record

ArticleJournal of neurology2026

Prediction of short-term and long-term responses to cladribine in relapsing-remitting multiple sclerosis: a Danish nationwide real-world study.

Stephan Bramow, Luigi Pontieri, Alex Heick, Anja Thormann, Tobias Sejbæk, Peter Vestergaard Rasmussen, Arkadiusz Weglewski, Shanga Hassan Qadir, Jeppe Romme Christensen, Camilla Mærsk-Møller and 10 more

Abstract read
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In one paragraph

Article in Journal of 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.

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

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

20 authors.

Stephan Bramow *Department of Neurology, Danish Multiple Sclerosis Center, Copenhagen University Hospital, Rigshospitalet Glostrup, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark. stephan.bramow@regionh.dk.ORCID http://orcid.org/0000-0001-9482-1771
Luigi Pontieri *Department of Neurology, The Danish Multiple Sclerosis Registry, Copenhagen University Hospital, Rigshospitalet Glostrup, Valdemar Hansens Vej 2, Entrance 8, 2nd floor, 2600, Glostrup, Denmark.
Alex HeickDepartment of Neurology, Danish Multiple Sclerosis Center, Copenhagen University Hospital, Rigshospitalet Glostrup, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark.
Anja ThormannDepartment of Neurology, Danish Multiple Sclerosis Center, Copenhagen University Hospital, Rigshospitalet Glostrup, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark.
Tobias SejbækDepartment of Neurology, Southwest Jutland Hospital, University Hospital of Southern Denmark, 6700, Esbjerg, Denmark.
Peter Vestergaard RasmussenDepartment of Neurology, Aarhus University Hospital, PJJ Boulevard 165, J504, 8200, Aarhus N, Denmark.
Arkadiusz WeglewskiDepartment of Neurology, Copenhagen University Hospital. Herlev and Gentofte, Herlev Ringvej 75, 2730, Herlev, Denmark.
Shanga Hassan QadirDepartment of Neurology, The Danish Multiple Sclerosis Registry, Copenhagen University Hospital, Rigshospitalet Glostrup, Valdemar Hansens Vej 2, Entrance 8, 2nd floor, 2600, Glostrup, Denmark.
Jeppe Romme ChristensenDepartment of Neurology, Danish Multiple Sclerosis Center, Copenhagen University Hospital, Rigshospitalet Glostrup, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark.
Camilla Mærsk-MøllerDepartment of Neurology, Aarhus University Hospital, PJJ Boulevard 165, J504, 8200, Aarhus N, Denmark.
Katrine ZachariassenDepartment of Neurology, Aarhus University Hospital, PJJ Boulevard 165, J504, 8200, Aarhus N, Denmark.
Jakob SchäferDepartment of Neurology, Aalborg University Hospital, Hospitalsbyen 1, 9260, Gistrup, Denmark.
Morten StilundDepartment of Neurology, Physiotherapy and Occupational Therapy, Gødstrup Hospital, Hospitalsparken 15, 7400, Herning, Denmark.
Henrik Boye JensenFaculty of Health Sciences, Institute of Regional Health Research, University of Southern Denmark, Campusvej 55, 5230, Odense M, Denmark.
Claudia Christina Hilt KristensenDepartment of Neurology, Aalborg University Hospital, Hospitalsbyen 1, 9260, Gistrup, Denmark.
Matthias KantDepartment of Neurology, Hospital of Southern Jutland, University of Southern Denmark, Kresten Philipsens Vej 15, 6200, Aabenraa, Denmark.
Finn SellebjergDepartment of Neurology, Danish Multiple Sclerosis Center, Copenhagen University Hospital, Rigshospitalet Glostrup, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark.
Per Soelberg Sørensen *Department of Neurology, Danish Multiple Sclerosis Center, Copenhagen University Hospital, Rigshospitalet Glostrup, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark.
Melinda Magyari *Department of Neurology, Danish Multiple Sclerosis Center, Copenhagen University Hospital, Rigshospitalet Glostrup, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark.
Danish Multiple Sclerosis Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cladribine is regarded highly efficacious in relapsing-remitting multiple sclerosis (RRMS). However, prediction of treatment response and optimal management remain elusive, particularly during long-term. We screened the Danish Multiple Sclerosis Registry for patients with RRMS who received ≥2 5-day treatment cycles of cladribine and were followed for >90 days. Annualised relapse rates (ARR) and activity parameters (relapses or MRI activity) were analysed from 90 days after the first dose (index) to year 3 (short-term) together with time-to-first 24-week confirmed disability worsening (CDW), CDW independent of relapses (PIRA), and activity/CDW (loss of "no evidence of disease activity", NEDA-3). Kaplan-Meier log-rank tests were validated in a subgroup who completed ≥4 five-day cladribine cycles before year 3 and contributed with >3 years follow-up (3YFS). Predicting covariables included age (< /≥ 45 years), pre-baseline activity, and short-term NEDA-3 status regarding 3YFS outcomes beyond year 3 (long-term). ARR declined significantly from ~0.55 in the year pre-baseline to ~0.23-0.25 from index to year 3. Younger age and pre-baseline activity predicted more frequent short-term activity. Pre-baseline activity additionally predicted short-term NEDA-3 loss. Short-term findings were consistent in 3YFS patients. CDW and PIRA were rare during short-term (~ 10%) and long-term (~ 20%), even in older patients. However, during long-term, NEDA-3 loss resumed steadily and this was largely unpredictable. While cladribine showed sustained short-term efficacy, treatment response appeared more favourable in older patients and patients without pre-baseline activity. Rare CDW and PIRA events warrant more research in cladribine for disability prevention. Optimal long-term management following cladribine treatment requires more research.

Indexed as

CladribineImmunosuppressive AgentsMultiple Sclerosis, Relapsing-RemittingAdultDenmarkFemaleFollow-Up StudiesHumansMaleMiddle AgedRegistriesTime FactorsTreatment OutcomeCladribineImmunosuppressive AgentsCladribineEfficacyLong-termMultiple sclerosisNEDA-3Prediction

Identifiers

What OpenQuestion holds

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Read underepoch 390

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 OpenQuestion graph.