Evidence map›Paper›PMID 36433775›Full record

ArticleMultiple sclerosis (Houndmills, Basingstoke, England)2023

Comparative effectiveness of cladribine tablets versus other oral disease-modifying treatments for multiple sclerosis: Results from MSBase registry.

Tim Spelman, Serkan Ozakbas, Raed Alroughani, Murat Terzi, Suzanne Hodgkinson, Guy Laureys, Tomas Kalincik, Anneke Van Der Walt, Bassem Yamout, Jeannette Lechner-Scott and 17 more

Open access · bronzeAbstract read
In one paragraph

Article in Multiple sclerosis (Houndmills, Basingstoke, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
4.3field-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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 35 citations in OpenAlex.

  1. Cladribine for people with multiple sclerosis.The Cochrane database of systematic reviews · 2026
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  13. Cladribine use trend in Latin America: the changes in patient profile impact in the drug effectiveness.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
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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

27 authors at 20 institutions in 13 countries.

Tim SpelmanMSBase Foundation, Melbourne, VIC, Australia.ORCID 0000-0001-9204-3216
Serkan OzakbasDokuz Eylul University, Izmir, Turkey.
Raed AlroughaniAl-Amiri Hospital, Kuwait City, Kuwait.ORCID 0000-0001-5436-5804
Murat TerziDepartment of Neurology, 19 Mayis University, Samsun, Turkey.
Suzanne HodgkinsonLiverpool Hospital, Sydney, NSW, Australia.
Guy LaureysUniversity Hospital Ghent, Ghent, Belgium.
Tomas KalincikMS Centre, Department of Neurology, Royal Melbourne Hospital, Melbourne, VIC, Australia/CORe, Department of Medicine, University of Melbourne, Melbourne, VIC, Australia.ORCID 0000-0003-3778-1376
Anneke Van Der WaltDepartment of Neuroscience, Central Clinical School, Monash University, Melbourne, VIC, Australia.ORCID 0000-0002-4278-7003
Bassem YamoutNeurology Institute, Harley Street Medical Center, Abu Dhabi, United Arab Emirates/American University of Beirut Medical Center, Beirut, Lebanon.
Jeannette Lechner-ScottSchool of Medicine and Public Health, University of Newcastle, Newcastle, NSW, Australia/Department of Neurology, John Hunter Hospital, Hunter New England Health, Newcastle, NSW, Australia.ORCID 0000-0002-3850-447X
Aysun SoysalBakirkoy Education and Research Hospital for Psychiatric and Neurological Diseases, Istanbul, Turkey.
Jens KuhleMultiple Sclerosis Centre, Neurology, Departments of Head, Spine and Neuromedicine, Biomedicine and Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland/Research Center for Clinical Neuroimmunology and Neuroscience (RC2NB), University Hospital and University of Basel, Basel, Switzerland.
Jose Luis Sanchez-MenoyoDepartment of Neurology, Galdakao-Usansolo University Hospital, Osakidetza-Basque Health Service, Biocruces-Bizkaia Health Research Institute, Galdakao, Spain.
Yolanda Blanco MorgadoCenter of Neuroimmunology, Service of Neurology, Hospital Clinic de Barcelona, Barcelona, Spain.
Daniele LA SpitaleriAzienda Ospedaliera di Rilievo Nazionale San Giuseppe Moscati Avellino, Avellino, Ital.
Vincent van PeschCliniques Universitaires Saint-Luc (UCLouvain), Brussels, Belgium.
Dana HorakovaDepartment of Neurology and Center of Clinical Neuroscience, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.ORCID 0000-0003-1915-0036
Radek AmpapaNemocnice Jihlava, Jihlava, Czech Republic.
Francesco PattiDepartment of Medical and Surgical Sciences and Advanced Technologies, GF Ingrassia, Catania, Italy.ORCID 0000-0002-6923-0846
Richard MacdonellDepartment of Neurology, Austin Health, Melbourne, VIC, Australia.
Abdullah Al-AsmiNeurology Unit, Department of Medicine, College of Medicine & Health Sciences and Sultan Qaboos University Hospital, Sultan Qaboos University (SQU), Al Khodh, Oman.
Oliver GerlachAcademic MS Center Zuyderland, Department of Neurology, Zuyderland Medical Center, Sittard-Geleen, The Netherlands/School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.
Jiwon OhDivision of Neurology, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada.ORCID 0000-0001-5519-6088
Ayse AltintasKoc University School of Medicine and Koc University Research Center for Translational Medicine (KUTTAM), Istanbul, Turkey.
Namita TundiaEMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA.
Schiffon L WongEMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA.
Helmut ButzkuevenMSBase Foundation, Melbourne, VIC, Australia/Department of Neuroscience, Central Clinical School, Monash University, Melbourne, VIC, Australia.
Monash University · AUResearch & Development Institute · USAmerican University of Beirut Medical Center · LBAmiri Hospital · KWAustin Health · AUAzienda Ospedaliera S.Giuseppe Moscati · ITBakırköy Psychiatric Hospital · TRCharles University · CZCliniques Universitaires Saint-Luc · BEDokuz Eylül University · TRGhent University Hospital · BEHospital Clínic de Barcelona · ESHospital de Galdakao · ESHospital Jihlava · CZJohn Hunter Hospital · AUKoç University · TRLiverpool Hospital · AUMaastricht University · NLOndokuz Mayıs University · TRSt. Michael's Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEffectiveness of cladribine tablets, an oral disease-modifying treatment (DMT) for multiple sclerosis (MS), was established in clinical trials and confirmed with real-world experience.

objectivesUse real-world data to compare treatment patterns and clinical outcomes in people with MS (pwMS) treated with cladribine tablets versus other oral DMTs.

methodsRetrospective treatment comparisons were based on data from the international MSBase registry. Eligible pwMS started treatment with cladribine, fingolimod, dimethyl fumarate, or teriflunomide tablets from 2018 to mid-2021 and were censored at treatment discontinuation/switch, death, loss to follow-up, pregnancy, or study period end. Treatment persistence was evaluated as time to discontinuation/switch; relapse outcomes included time to first relapse and annualized relapse rate (ARR).

resultsCohorts included 633 pwMS receiving cladribine tablets, 1195 receiving fingolimod, 912 receiving dimethyl fumarate, and 735 receiving teriflunomide. Individuals treated with fingolimod, dimethyl fumarate, or teriflunomide switched treatment significantly more quickly than matched cladribine tablet cohorts (adjusted hazard ratio (95% confidence interval): 4.00 (2.54-6.32), 7.04 (4.16-11.93), and 6.52 (3.79-11.22), respectively). Cladribine tablet cohorts had significantly longer time-to-treatment discontinuation, time to first relapse, and lower ARR, compared with other oral DMT cohorts.

conclusionCladribine tablets were associated with a significantly greater real-world treatment persistence and more favorable relapse outcomes than all oral DMT comparators.

Indexed as

Multiple SclerosisMultiple Sclerosis, Relapsing-RemittingCladribineCrotonatesDimethyl FumarateFingolimod HydrochlorideHumansHydroxybutyratesImmunosuppressive AgentsNitrilesRecurrenceRegistriesRetrospective StudiesTabletsToluidinesCladribineCrotonatesDimethyl FumarateFingolimod HydrochlorideHydroxybutyratesImmunosuppressive AgentsNitrilesTabletsteriflunomideToluidinesdisabilitydiscontinuationMSreal-world dataregistryrelapseswitching

Identifiers

PMID36433775
PMCPMC9925904
OpenAlexW4310295951

What OpenQuestion 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 OpenQuestion graph.