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dc.rights.licenseopenen_US
dc.contributor.authorVUKUSIC, Sandra
dc.contributor.authorROLLOT, Fabien
dc.contributor.authorCASEY, Romain
dc.contributor.authorPIQUE, Julie
dc.contributor.authorMARIGNIER, Romain
dc.contributor.authorMATHEY, Guillaume
dc.contributor.authorEDAN, Gilles
dc.contributor.authorBRASSAT, David
hal.structure.identifierNeurocentre Magendie : Physiopathologie de la Plasticité Neuronale [U1215 Inserm - UB]
dc.contributor.authorRUET, Aurelie
dc.contributor.authorDE SEZE, Jerome
dc.contributor.authorMAILLART, Elisabeth
dc.contributor.authorZEPHIR, Helene
dc.contributor.authorLABAUGE, Pierre
dc.contributor.authorDERACHE, Nathalie
dc.contributor.authorLEBRUN-FRENAY, Christine
dc.contributor.authorMOREAU, Thibault
dc.contributor.authorWIERTLEWSKI, Sandrine
dc.contributor.authorBERGER, Eric
dc.contributor.authorMOISSET, Xavier
dc.contributor.authorRICO-LAMY, Audrey
dc.contributor.authorSTANKOFF, Bruno
dc.contributor.authorBENSA, Caroline
dc.contributor.authorTHOUVENOT, Eric
dc.contributor.authorHEINZLEF, Olivier
dc.contributor.authorAL-KHEDR, Abdullatif
dc.contributor.authorBOURRE, Bertrand
dc.contributor.authorVAILLANT, Mathieu
dc.contributor.authorCABRE, Philippe
dc.contributor.authorMONTCUQUET, Alexis
dc.contributor.authorWAHAB, Abir
dc.contributor.authorCAMDESSANCHE, Jean-Philippe
dc.contributor.authorTOURBAH, Ayman
dc.contributor.authorGUENNOC, Anne-Marie
dc.contributor.authorHANKIEWICZ, Karolina
dc.contributor.authorPATRY, Ivania
dc.contributor.authorNIFLE, Chantal
dc.contributor.authorMAUBEUGE, Nicolas
dc.contributor.authorLABEYRIE, Celine
dc.contributor.authorVERMERSCH, Patrick
dc.contributor.authorLAPLAUD, David-Axel
dc.date.accessioned2023-07-17T09:55:29Z
dc.date.available2023-07-17T09:55:29Z
dc.date.issued2020-01-01
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/183403
dc.description.abstractEnImportance: 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. © 2019 American Medical Association. All rights reserved.
dc.description.sponsorshipObservatoire Français de la Sclérose en Plaques - ANR-10-COHO-0002en_US
dc.language.isoENen_US
dc.subject.enAdolescent
dc.subject.enAdult
dc.subject.enFemale
dc.subject.enFrance
dc.subject.enHumans
dc.subject.enImmunocompromised Host
dc.subject.enImmunologic Factors
dc.subject.enIncidence
dc.subject.enJC Virus
dc.subject.enLeukoencephalopathy
dc.subject.enProgressive Multifocal
dc.subject.enMale
dc.subject.enMultiple Sclerosis
dc.subject.enRelapsing-Remitting
dc.subject.enNatalizumab
dc.subject.enRegistries
dc.subject.enRisk Factors
dc.subject.enYoung Adult
dc.subject.enClinical evaluation
dc.subject.enClinical trial
dc.subject.enData analysis
dc.subject.enExposure
dc.subject.enFrance
dc.subject.enGroups by age
dc.subject.enMajor clinical study
dc.subject.enMulticenter study
dc.subject.enNeurologist
dc.subject.enObservational study
dc.subject.enPriority journal
dc.subject.enProgressive multifocal leukoencephalopathy
dc.subject.enQuestionnaire
dc.subject.enRegister
dc.subject.enSex
dc.subject.enAdolescent
dc.subject.enImmunocompromised patient
dc.subject.enImmunology
dc.title.enProgressive Multifocal Leukoencephalopathy Incidence and Risk Stratification among Natalizumab Users in France
dc.title.alternativeJAMA Neurolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1001/jamaneurol.2019.2670en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed31479149en_US
bordeaux.journalJAMA Neurologyen_US
bordeaux.page94-102en_US
bordeaux.volume77en_US
bordeaux.hal.laboratoriesNeurocentre Magendie - U1215en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamRelations glie-neuroneen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
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