Evidence map›Paper›PMID 33712515›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2021

Impact of previous disease-modifying treatment on effectiveness and safety outcomes, among patients with multiple sclerosis treated with alemtuzumab.

Steffen Pfeuffer, Tobias Ruck, Refik Pul, Leoni Rolfes, Catharina Korsukewitz, Marc Pawlitzki, Brigitte Wildemann, Luisa Klotz, Christoph Kleinschnitz, Antonio Scalfari and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of neurology, neurosurgery, and psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
4.4field-weighted citation impact, top 5% of its field
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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 31 citations in OpenAlex.

  1. Pooled it
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  3. The Art of Sequencing Disease-Modifying Therapies in Multiple Sclerosis.Neurology(R) neuroimmunology & neuroinflammation · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Steffen Pfeuffer *Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany steffen.pfeuffer@ukmuenster.de.ORCID 0000-0001-5171-4845
Tobias Ruck *Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.
Refik PulDepartment of Neurology, Universitat Duisburg-Essen, Duisburg, Germany.
Leoni RolfesDepartment of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.ORCID 0000-0003-4494-951X
Catharina KorsukewitzDepartment of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.
Marc PawlitzkiDepartment of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.
Brigitte WildemannDivision of Molecular Neuroimmunology, Department of Neurology, University Hospital Heidelberg, Heidelberg, Germany.
Luisa KlotzDepartment of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.
Christoph KleinschnitzDepartment of Neurology, Universitat Duisburg-Essen, Duisburg, Germany.
Antonio ScalfariCentre for Neuroscience, Division of Experimental Medicine, Hammersmith Hospital, Imperial College London, London, UK.
Heinz Wiendl *Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.
Sven G Meuth *Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.
University Hospital Münster · DEUniversity of Duisburg-Essen · DEHeidelberg University · DEImperial College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAlemtuzumab is effective in patients with active multiple sclerosis but has a complex safety profile, including the development of secondary autoimmunity. Most of patients enrolled in randomised clinical trials with alemtuzumab were either treatment naïve or pretreated with injectable substances. Other previous disease-modifying treatments (DMTs) were not used in the study cohorts, and therefore, associated risks might yet remain unidentified.

methodsWe retrospectively evaluated a prospective dual-centre alemtuzumab cohort of 170 patients. We examined the baseline characteristics as well as safety and effectiveness outcomes, including the time to first relapse, the time to 3 months confirmed disability worsening and the time to secondary autoimmunity.

resultsThe regression analysis showed that, among all previously used DMTs, the pretreatment with fingolimod (n=33 HRs for the time to first relapse (HR 5.420, 95% CI 2.520 to 11.660; p<0.001)) and for the time to worsening of disability (HR 7.676, 95% CI 2.870 to 20.534; p<0.001). Additionally, patients pretreated with fingolimod were more likely to experience spinal relapses (55% vs 10% among previously naïve patients; p<0.001) and had an increased risk of secondary autoimmunity (HR 5.875, 95% CI 2.126 to 16.27; p<0.001).

conclusionIn the real-world setting, we demonstrated suboptimal disease control and increased risk of secondary autoimmunity following alemtuzumab, among patients previously treated with fingolimod. These data can provide guidance for improving MS therapeutic management.

Indexed as

AdultAlemtuzumabFemaleHumansImmunosuppressive AgentsMaleMultiple SclerosisProspective StudiesRetreatmentRetrospective StudiesTreatment OutcomeYoung AdultAlemtuzumabImmunosuppressive Agents

Identifiers

PMID33712515
PMCPMC8372391
OpenAlexW3133528057

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.