Evidence map›Paper›PMID 35217934›Full record

ArticleNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2022

Comparative Effectiveness of Natalizumab Versus Anti-CD20 in Highly Active Relapsing-Remitting Multiple Sclerosis After Fingolimod Withdrawal.

Fabien Rollot, Justine Couturier, Romain Casey, Sandrine Wiertlewski, Marc Debouverie, Jean Pelletier, Jérôme De Sèze, Pierre Labauge, Aurélie Ruet, Eric Thouvenot and 24 more

Open access · bronzeAbstract read
In one paragraph

Article in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Rituximab for people with multiple sclerosis.The Cochrane database of systematic reviews · 2025
    Pooled it
  2. The Art of Sequencing Disease-Modifying Therapies in Multiple Sclerosis.Neurology(R) neuroimmunology & neuroinflammation · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Observational
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

34 authors at 20 institutions in 2 countries.

Fabien RollotUniversité de Lyon, Université Claude Bernard, Lyon 1, Lyon, France. Fabien.rollot@chu-lyon.fr.ORCID 0000-0002-5752-2331
Justine CouturierService de Neurologie, CHU Nantes, Nantes, France.
Romain CaseyUniversité de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
Sandrine WiertlewskiService de Neurologie, CHU Nantes, Nantes, France.
Marc DebouverieService de Neurologie, Centre Hospitalier Régional Et Universitaire de Nancy, Université de Lorraine, 4360 APEMAC, Vandoeuvre-Lès-Nancy, EA, France.
Jean PelletierAix Marseille University, APHM, Hôpital de La Timone, Pôle de Neurosciences Cliniques, Service de Neurologie, CEMEREM, 13005, Marseille, France.
Jérôme De SèzeService de Neurologie Et Centre d'Investigation Clinique, CHU de Strasbourg, INSERM 1434, Strasbourg, France.
Pierre LabaugeService de Neurologie, CHU de Montpellier, Montpellier, France.
Aurélie RuetService de Neurologie, CHU de Bordeaux, Bordeaux, France.
Eric ThouvenotService de Neurologie, CHU de Nîmes, Nîmes, France.
Jonathan CironService de Neurologie, CHU de Toulouse, Hôpital Pierre-Paul Riquet, CRC-SEP, Toulouse, France.
Eric BergerService de Neurologie, CHU de Besançon, Besançon, France.
Olivier GoutService de Neurologie, Hôpital Fondation A de Rothschild, Paris, France.
Pierre ClavelouService de Neurologie, CHU de Clermont-Ferrand, Clermont-Ferrand, France.
Bruno StankoffService de Neurologie, CHU Saint-Antoine, Paris, France.
Olivier CasezService de Neurologie, CHU de Grenoble, Grenoble, France.
Bertrand BourreService de Neurologie, CHU de Rouen, Rouen, France.
Hélène ZephirPôle Des Neurosciences Et de L'appareil Locomoteur, CRC-SEP, Hôpital Roger Salengro, Université de Lille, Inserm U1172, Lille, France.
Thibault MoreauService de Neurologie, CHU de Dijon, Dijon, France.
Christine Lebrun-FrenayService de Neurologie, Neurologie Pasteur 2, CHU de Nice, Université Nice Cote d'Azur UR2CA-URRIS, Nice, France.
Elisabeth MaillartDépartement de Neurologie, APHP, Hôpital Pitié-Salpêtrière, Paris, France.
Gilles EdanService de Neurologie, CHU Pontchaillou, Rennes, France.
Jean-Philippe NeauService de Neurologie, CHU La Milétrie, Poitiers, France.
Alexis MontcuquetService de Neurologie, CHU de Limoges, Limoges, France.
Philippe CabreService de Neurologie, CHU de Fort de France, Fort de France, France.
Jean-Philippe CamdessanchéService de Neurologie, Hôpital Nord, CHU Saint-Étienne, Saint-Etienne, France.
Gilles DeferService de Neurologie, Centre Expert SEP, CHU de Caen, Université Normandie, Caen, France.
Haifa Ben NasrService de Neurologie, Hôpital Sud Francilien, Corbeil Essonnes, France.
Aude MauroussetService de Neurologie, CHU Bretonneau, Tours, France.
Karolina HankiewiczService de Neurologie, CH de Saint-Denis, Saint-Denis, France.
Corinne PottierService de Neurologie, Hôpital René Dubos, Pontoise, France.
Emmanuelle LerayUniversité de Rennes/EHESP, REPERES - EA, 7449, Rennes, France.
Sandra VukusicUniversité de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
David-Axel LaplaudService de Neurologie, CHU Nantes, Nantes, France. david.laplaud@univ-nantes.fr.
Inserm · FRUniversité Claude Bernard Lyon 1 · FRCentre National de la Recherche Scientifique · FRSorbonne Université · FRAix-Marseille Université · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier René-Dubos · FRCentre Hospitalier Saint-Denis · FRCentre Hospitalier Sud Francilien · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Limoges · FRCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Nice · FRCentre Hospitalier Universitaire de Poitiers · FRCentre Hospitalier Universitaire de Rouen · FRCentre Hospitalier Universitaire de Tours · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In France, two therapeutic strategies can be offered after fingolimod (FNG) withdrawal to highly active relapsing-remitting multiple sclerosis (RRMS) patients: natalizumab (NTZ) or anti-CD20. We compared the effectiveness of these two strategies as a switch for FNG within the OFSEP database. The primary endpoint was the time to first relapse. Other outcomes were the relapse rates over 3-month periods, time to worsening the EDSS score, proportion of patients with worsened 24-month MRI, time to treatment discontinuation, and incidence rates of serious adverse events. The dynamics of event rates over time were modeled using multidimensional penalized splines, allowing the possibility to model the effects of covariates in a flexible way, considering non-linearity and interactions. A total of 740 patients were included (337 under anti-CD20 and 403 under NTZ). There was no difference between the two treatments regarding the dynamic of the first occurrence of relapse, with a monthly probability of 5.0% at initiation and 1.0% after 6 months. The rate of EDSS worsening increased in both groups until 6 months and then decreased. No difference in the proportion of patients with new T2 lesions at 24 months was observed. After 18 months of follow-up, a greater risk of NTZ discontinuation was found compared to anti-CD20. This study showed no difference between NTZ and anti-CD20 after the FNG switch regarding the clinical and radiological activity. The effect of these treatments was optimal after 6 months and there was more frequent discontinuation of NTZ after 18 months, probably mainly related to JC virus seroconversions.

Indexed as

Multiple SclerosisMultiple Sclerosis, Relapsing-RemittingAntigens, CD20Fingolimod HydrochlorideHumansImmunologic FactorsImmunosuppressive AgentsNatalizumabRecurrenceAntigens, CD20Fingolimod HydrochlorideImmunologic FactorsImmunosuppressive AgentsNatalizumabAnti-CD20EffectivenessFingolimodFlexible modelMultiple sclerosisNatalizumabTherapeutics

Identifiers

PMID35217934
PMCPMC9226262
OpenAlexW4214753683

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.