Evidence map›Paper›PMID 31479149›Full record

Observational studyJAMA neurology2020

Progressive Multifocal Leukoencephalopathy Incidence and Risk Stratification Among Natalizumab Users in France.

Sandra Vukusic, Fabien Rollot, Romain Casey, Julie Pique, Romain Marignier, Guillaume Mathey, Gilles Edan, David Brassat, Aurélie Ruet, Jérôme De Sèze and 31 more

Open access · bronzeAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in JAMA neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 3 pooled it
3.5field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 3 syntheses or guidelines pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Comparative safety of high-efficacy disease-modifying therapies in relapsing-remitting multiple sclerosis: a systematic review and network meta-analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Comparative Effectiveness of Natalizumab Versus Anti-CD20 in Highly Active Relapsing-Remitting Multiple Sclerosis After Fingolimod Withdrawal.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Article
  15. Article
  16. Risk for Postmarket Black Box Warnings in FDA-Approved Monoclonal Antibodies.Mayo Clinic proceedings. Innovations, quality & outcomes · 2022
    Article
  17. Article
  18. Review
  19. Article
  20. Review
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

41 authors at 20 institutions in 2 countries.

Sandra VukusicUniversité Claude Bernard Lyon 1, Faculté de Médecine Lyon Est, Lyon, France.
Fabien RollotUniversité Claude Bernard Lyon 1, Faculté de Médecine Lyon Est, Lyon, France.
Romain CaseyUniversité Claude Bernard Lyon 1, Faculté de Médecine Lyon Est, Lyon, France.
Julie PiqueUniversité Claude Bernard Lyon 1, Faculté de Médecine Lyon Est, Lyon, France.
Romain MarignierUniversité Claude Bernard Lyon 1, Faculté de Médecine Lyon Est, Lyon, France.
Guillaume MatheyDepartment of Neurology, Nancy University Hospital, Nancy, France.
Gilles EdanCHU Pontchaillou, CIC1414 INSERM, Rennes, France.
David BrassatDepartment of Neurology, CHU de Toulouse, Toulouse, France.
Aurélie RuetUniversity of Bordeaux, Bordeaux, France.
Jérôme De SèzeClinical Investigation Center, Department of Neurology, CHU de Strasbourg, INSERM 1434, Strasbourg, France.
Elisabeth MaillartDepartment of Neurology, Assistance Publique des Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Paris, France.
Hélène ZéphirLIRIC (Lille Inflammation Research International Center), University of Lille, CHU de Lille, INSERM UMR995, Lille, France.
Pierre LabaugeCHU de Montpellier, MS Unit, Montpellier, France.
Nathalie DeracheDepartment of Neurology, CHU de la Côte de Nacre, Caen, France.
Christine Lebrun-FrenayCHU de Nice, Université Nice Côte d'Azur, CRCSEP Nice, Neurologie Pasteur 2, Nice, France.
Thibault MoreauDepartment of Neurology, CHU de Dijon, EA4184, Dijon, France.
Sandrine WiertlewskiCHU de Nantes, Service de Neurologie, CIC015 INSERM, Nantes, France.
Eric BergerDepartment of Neurology, CHU de Besançon, Besançon, France.
Xavier MoissetDepartment of Neurology, Neuro-Dol, CHU Clermont-Ferrand, Université Clermont Auvergne, INSERM U1107, Clermont-Ferrand, France.
Audrey Rico-LamyPôle de Neurosciences Cliniques, Service de Neurologie, APHM, Hôpital de la Timone, Marseille, France.
Bruno StankoffBrain and Spine Institute, Sorbonne Universités, UPMC Paris 06, ICM, Hôpital de la Pitié Salpêtrière, INSERM UMR S 1127, CNRS UMR 7225, Paris, France.
Caroline BensaDepartment of Neurology, Fondation Rothschild, Paris, France.
Eric ThouvenotDepartment of Neurology, CHU de Nîmes, Nîmes, France.
Olivier HeinzlefDepartment of Neurology, Hôpital de Poissy, Poissy, France.
Abdullatif Al-KhedrDepartment of Neurology, CHU d'Amiens, Amiens, France.
Bertrand BourreDepartment of Neurology, CHU de Rouen, Rouen, France.
Mathieu VaillantDepartment of Neurology, CHU Grenoble Alpes, Grenoble, France.
Philippe CabreDepartment of Neurology, CHU de la Martinique, Fort-de-France, France.
Alexis MontcuquetDepartment of Neurology, CHU de Limoges, Hôpital Dupuytren, Limoges, France.
Abir WahabDepartment of Neurology, Assistance Publique des Hôpitaux de Paris, Hôpital Henri Mondor, Université Paris Est, Créteil, France.
Jean-Philippe CamdessanchéDepartment of Neurology, CHU de Saint-Étienne, Hôpital Nord, Saint-Étienne, France.
Ayman TourbahDepartment of Neurology, CHU de Reims, Faculté de Médecine de Reims, URCA, Reims, France.
Anne-Marie GuennocDepartment of Neurology, CHU de Tours, Hôpital Bretonneau, CRC SEP, Tours, France.
Karolina HankiewiczDepartment of Neurology, Hôpital Pierre Delafontaine, Centre Hospitalier de Saint-Denis, Saint-Denis, France.
Ivania PatryDepartment of Neurology, Hôpital Sud Francilien, Corbeil-Essonnes, France.
Chantal NifleDepartment of Neurology, Centre Hospitalier de Versailles, Le Chesnay, France.
Nicolas MaubeugeDepartment of Neurology, CHU de Poitiers, Hôpital La Milétrie, Poitiers, France.
Céline LabeyrieDepartment of Neurology, CHU de Bicêtre, Le Kremlin-Bicêtre, France.
Patrick VermerschLIRIC (Lille Inflammation Research International Center), University of Lille, CHU de Lille, INSERM UMR995, Lille, France.
David-Axel LaplaudCHU de Nantes, Service de Neurologie, CIC015 INSERM, Nantes, France.
OFSEP Investigators
Inserm · FRUniversité Claude Bernard Lyon 1 · FRCentre National de la Recherche Scientifique · FRBicêtre Hospital · FRCentre Hospitalier de Versailles · FRCentre Hospitalier Intercommunal de Poissy · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Saint-Denis · FRCentre Hospitalier Sud Francilien · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Limoges · FRCentre Hospitalier Universitaire de Martinique · MQCentre Hospitalier Universitaire de Nice · FRCentre Hospitalier Universitaire de Poitiers · FRCentre Hospitalier Universitaire de Reims · FRCentre Hospitalier Universitaire de Rouen · FRCentre Hospitalier Universitaire de Toulouse · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Risk of developing progressive multifocal leukoencephalopathy (PML) is the major barrier to using natalizumab for patients with multiple sclerosis (MS). To date, the association of risk stratification with PML incidence has not been evaluated. Objective: To describe the temporal evolution of PML incidence in France before and after introduction of risk minimization recommendations in 2013. Design, Setting, and Participants: This observational study used data in the MS registry OFSEP (Observatoire Français de la Sclérose en Plaques) collected between April 15, 2007, and December 31, 2016, by participating MS expert centers and MS-dedicated networks of neurologists in France. Patients with an MS diagnosis according to current criteria, regardless of age, were eligible, and those exposed to at least 1 natalizumab infusion (n = 6318) were included in the at-risk population. A questionnaire was sent to all centers, asking for a description of their practice regarding PML risk stratification. Data were analyzed in July 2018. Exposures: Time from the first natalizumab infusion to the occurrence of PML, natalizumab discontinuation plus 6 months, or the last clinical evaluation. Main Outcomes and Measures: Incidence was the number of PML cases reported relative to the person-years exposed to natalizumab. A Poisson regression model for the 2007 to 2016 period estimated the annual variation in incidence and incidence rate ratio (IRR), adjusted for sex and age at treatment initiation and stratified by period (2007-2013 and 2013-2016). Results: In total, 6318 patients were exposed to natalizumab during the study period, of whom 4682 (74.1%) were female, with a mean (SD [range]) age at MS onset of 28.5 (9.1 [1.1-72.4]) years; 45 confirmed incident cases of PML were diagnosed in 22 414 person-years of exposure. The crude incidence rate for the whole 2007 to 2016 period was 2.00 (95% CI, 1.46-2.69) per 1000 patient-years. Incidence significantly increased by 45.3% (IRR, 1.45; 95% CI, 1.15-1.83; P = .001) each year before 2013 and decreased by 23.0% (IRR, 0.77; 95% CI, 0.61-0.97; P = .03) each year from 2013 to 2016. Conclusions and Relevance: The results of this study suggest, for the first time, a decrease in natalizumab-associated PML incidence since 2013 in France that may be associated with a generalized use of John Cunningham virus serologic test results; this finding appears to support the continuation and reinforcement of educational activities and risk-minimization strategies in the management of disease-modifying therapies for multiple sclerosis.

Indexed as

AdolescentAdultFemaleFranceHumansImmunocompromised HostImmunologic FactorsIncidenceJC VirusLeukoencephalopathy, Progressive MultifocalMaleMultiple Sclerosis, Relapsing-RemittingNatalizumabRegistriesRisk FactorsYoung AdultImmunologic FactorsNatalizumab

Identifiers

PMID31479149
PMCPMC6724170
OpenAlexW2972029908

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.