Evidence map›Paper›PMID 35107597›Full record

Observational studyJournal of neurology2022

Effectiveness of rituximab vs. ocrelizumab for the treatment of primary progressive multiple sclerosis: a real-world observational study.

Carmen Alcalá, Carlos Quintanilla-Bordás, Francisco Gascón, Ángel Perez Sempere, Laura Navarro, María Carcelén-Gadea, Lamberto Landete, Javier Mallada, Emmanuel Cañizares, Antonio Belenguer and 8 more

Open access · greenAbstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Journal of neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 4 pooled it
3.4field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 4 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Rituximab for people with multiple sclerosis.The Cochrane database of systematic reviews · 2025
    Pooled it
  3. Real-world evaluation of ocrelizumab in multiple sclerosis: A systematic review.Annals of clinical and translational neurology · 2023
    Pooled it
  4. Pooled it
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  7. Review
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  9. Observational
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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

18 authors at 9 institutions in 1 country.

Carmen Alcalá *Neuroimmunology Unit, Polytechnic and University Hospital La Fe València, Avda. Fernando Abril Martorell, 106, 46026, Valencia, Spain.
Carlos Quintanilla-Bordás *Neuroimmunology Unit, Polytechnic and University Hospital La Fe València, Avda. Fernando Abril Martorell, 106, 46026, Valencia, Spain. carlosqb@gmail.com.ORCID http://orcid.org/0000-0002-4681-2456
Francisco GascónNeurology Service, Clinic University Hospital of València, Valencia, Spain.
Ángel Perez SempereNeurology Service, University General Hospital of Alacant, Alicante, Spain.
Laura NavarroNeurology Service, University General Hospital of Elx, Elche, Spain.
María Carcelén-GadeaNeurology Service, University General Hospital of València, Valencia, Spain.
Lamberto LandeteNeurology Service, University Dr. Peset University Hospital of València, Valencia, Spain.
Javier MalladaNeurology Service, University General Hospital of Elda, Elda, Spain.
Emmanuel CañizaresNeurology Unit, La Ribera University Hospital, Alzira, Spain.
Antonio BelenguerNeurology Service, University General Hospital of Castelló, Castelló de la Plana, Spain.
Sara CarrataláNeuroimmunology Unit, Polytechnic and University Hospital La Fe València, Avda. Fernando Abril Martorell, 106, 46026, Valencia, Spain.
José Andrés DomínguezNeurology Service, Clinic University Hospital of València, Valencia, Spain.
Francisco Carlos Pérez-MirallesNeuroimmunology Unit, Polytechnic and University Hospital La Fe València, Avda. Fernando Abril Martorell, 106, 46026, Valencia, Spain.
Sara Gil-PerotínNeuroimmunology Unit, Polytechnic and University Hospital La Fe València, Avda. Fernando Abril Martorell, 106, 46026, Valencia, Spain.
Raquel GasquéNeuroimmunology Unit, Polytechnic and University Hospital La Fe València, Avda. Fernando Abril Martorell, 106, 46026, Valencia, Spain.
Laura CubasNeuroimmunology Unit, Polytechnic and University Hospital La Fe València, Avda. Fernando Abril Martorell, 106, 46026, Valencia, Spain.
Jéssica CastilloNeuroimmunology Unit, Polytechnic and University Hospital La Fe València, Avda. Fernando Abril Martorell, 106, 46026, Valencia, Spain.
Bonaventura CasanovaNeuroimmunology Unit, Polytechnic and University Hospital La Fe València, Avda. Fernando Abril Martorell, 106, 46026, Valencia, Spain.
Hospital Universitari i Politècnic La Fe · ESHospital Clínico Universitario de Valencia · ESHospital de La Ribera · ESHospital General de Elda · ESHospital General Universitari de Castelló · ESHospital General Universitario de Alicante Doctor Balmis · ESHospital General Universitario de Elche · ESHospital General Universitario De Valencia · ESHospital Universitario Doctor Peset · ES

Funding

Instituto de Salud Carlos III PI20/01446
6 · The paper itself

Abstract

introductionOcrelizumab, an antiCD-20 antibody, is the only drug approved to treat patients with primary progressive multiple sclerosis (pwPPMS). Not all candidates receive this treatment due to prescription limitations. Rituximab, another antiCD-20 antibody, has been used off-label in pwPPMS before and after ocrelizumab approval. However, studies comparing effectiveness of both drugs are lacking.

objectiveTo evaluate effectiveness of rituximab and ocrelizumab in pwPPMS under real-life conditions.

methodsWe conducted a multicentric observational study of pwPPMS that started ocrelizumab or rituximab according to clinical practice, with a minimum follow-up of 1 year. Data was collected prospectively and retrospectively. Primary outcome was time to confirmed disability progression at 3 months (CDW). Secondary outcome was serum neurofilament light chain levels (sNFL) at the end of follow-up.

results95 out 111 pwPPMS fulfilled inclusion criteria and follow-up data availability: 49 (51.6%) received rituximab and 46 (48.4%) ocrelizumab. Rituximab-treated patients had significantly higher baseline EDSS, disease duration and history of previous disease-modifying treatment (DMT) than ocrelizumab-treated patients. After a mean follow-up of 18.3 months (SD 5.9), 26 patients experienced CDW (21.4%); 15 (30.6%) in the rituximab group; and 11 (23.9%) in the ocrelizumab group. Survival analysis revealed no differences in time to CDW. sNFL were measured in 60 patients and no differences between groups were found.

interpretationWe provide real-world evidence of effectiveness of ocrelizumab and rituximab in pwPPMS. No differences in time to CDW were found between treatments. However, this study cannot establish equivalence of treatments and warrant clinical trial to confirm our findings.

Indexed as

Multiple SclerosisMultiple Sclerosis, Chronic ProgressiveMultiple Sclerosis, Relapsing-RemittingAntibodies, Monoclonal, HumanizedHumansImmunologic FactorsRetrospective StudiesRituximabAntibodies, Monoclonal, HumanizedImmunologic FactorsocrelizumabRituximabPPMS treatment ocrelizumab rituximab real-world effectiveness

Identifiers

PMID35107597
OpenAlexW4210725630

What OpenQuestion holds

Textmetadata
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.