Evidence map›Paper›PMID 30785358›Full record

Trial reportMultiple sclerosis (Houndmills, Basingstoke, England)2020

Immune thrombocytopenia in alemtuzumab-treated MS patients: Incidence, detection, and management.

Adam Cuker, Ann D Bass, Congor Nadj, Mark A Agius, Brian Steingo, Krzysztof W Selmaj, Timothy Thoits, Alexandre Guerreiro, Bart Van Wijmeersch, Tjalf Ziemssen and 7 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Multiple sclerosis (Houndmills, Basingstoke, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 3 pooled it
6.7field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 3 syntheses or guidelines pooled it, 54 citations in OpenAlex.

  1. Alemtuzumab and thrombotic thrombocytopenic purpura: Analysis of an international surveillance database and systematic literature review.Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis · 2025
    Pooled it
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  9. Monoclonal Antibodies in the Treatment of Relapsing Multiple Sclerosis: an Overview with Emphasis on Pregnancy, Vaccination, and Risk Management.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Review
  10. Review
  11. Article
  12. Monoclonal Antibodies as Neurological Therapeutics.Pharmaceuticals (Basel, Switzerland) · 2021
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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

17 authors at 12 institutions in 5 countries.

Adam CukerDepartments of Medicine and Pathology & Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Ann D BassNeurology Center of San Antonio, San Antonio, TX, USA.
Congor NadjInstitute of Neurology, Novi Sad, Serbia.
Mark A AgiusWoodland Clinic, Dignity Health, Woodland, CA, USA.
Brian SteingoFort Lauderdale MS Center, Pompano Beach, FL, USA.
Krzysztof W SelmajUniversity of Warmia and Mazury in Olsztyn, Olsztyn, Poland.
Timothy ThoitsCollege of Human Medicine, MSU Spectrum Health, Grand Rapids, MI, USA.
Alexandre GuerreiroInstituto de Doenças Neurológicas do Hospital Mãe de Deus, Porto Alegre, Brazil.
Bart Van WijmeerschRehabilitation and MS Centre Overpelt, BIOMED, University of Hasselt, Hasselt, Belgium.
Tjalf ZiemssenCenter of Clinical Neuroscience, University Hospital Carl Gustav Carus, Dresden, Germany.
Sven G MeuthDepartment of Neurology, University of Münster, Münster, Germany.
Christopher C LaGankeNorth Central Neurology Associates, Cullman, AL, USA.
Karthinathan ThangaveluSanofi, Cambridge, MA, USA.
Claudio E RodriguezSanofi, Cambridge, MA, USA.
Darren P BakerSanofi, Cambridge, MA, USA.
David H MargolinSanofi, Cambridge, MA, USA.
Ann JannsensDepartment of Haematology, University Hospitals Leuven, Leuven, Belgium.
Sanofi (United States) · USDignity Health · USHasselt University · BEHospital Mãe de Deus · BRHospital of the University of Pennsylvania · USKU Leuven · BESpectrum Health · USUniversity Hospital Carl Gustav Carus · DEUniversity of Münster · DEUniversity of Warmia and Mazury in Olsztyn · PLUrology Associates · USUrology San Antonio · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlemtuzumab is a highly effective therapy for relapsing-remitting multiple sclerosis (RRMS), and immune thrombocytopenia (ITP) has been identified as a risk.

objectiveTo examine ITP incidence, treatment, and outcomes during the clinical development of alemtuzumab for RRMS and discuss postmarketing experience outside clinical trials.

methodsCAMMS223 and Comparison of Alemtuzumab and Rebif

resultsOf 1485 alemtuzumab-treated MS patients in the clinical development program, 33 (2.2%) developed ITP (alemtuzumab 12 mg, 24 [2.0%]; alemtuzumab 24 mg, 9 [3.3%]) over median 6.1 years of follow-up after the first infusion; most had a sustained response to first-line ITP therapy with corticosteroids, platelets, and/or intravenous immunoglobulin. All cases occurred within 48 months of the last alemtuzumab infusion. Postmarketing surveillance data suggest that the ITP incidence is not higher in clinical practice than in clinical trials.

conclusionAlemtuzumab-associated ITP occurs in approximately 2% of patients and is responsive to therapy. Careful monitoring is key for detection and favorable outcomes.

Indexed as

Purpura, Thrombocytopenic, IdiopathicAdultAlemtuzumabFemaleFollow-Up StudiesHumansImmunologic FactorsIncidenceInterferon beta-1aMaleMiddle AgedMultiple Sclerosis, Relapsing-RemittingAlemtuzumabImmunologic FactorsInterferon beta-1aAlemtuzumabdisease-modifying therapyimmune thrombocytopeniarelapsing-remitting multiple sclerosissafety

Identifiers

PMID30785358
PMCPMC6950888
OpenAlexW2917311835

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.