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

被引:0
|
作者
Fabien Rollot
Justine Couturier
Romain Casey
Sandrine Wiertlewski
Marc Debouverie
Jean Pelletier
Jérôme De Sèze
Pierre Labauge
Aurélie Ruet
Eric Thouvenot
Jonathan Ciron
Eric Berger
Olivier Gout
Pierre Clavelou
Bruno Stankoff
Olivier Casez
Bertrand Bourre
Hélène Zephir
Thibault Moreau
Christine Lebrun-Frenay
Elisabeth Maillart
Gilles Edan
Jean-Philippe Neau
Alexis Montcuquet
Philippe Cabre
Jean-Philippe Camdessanché
Gilles Defer
Haifa Ben Nasr
Aude Maurousset
Karolina Hankiewicz
Corinne Pottier
Emmanuelle Leray
Sandra Vukusic
David-Axel Laplaud
机构
[1] Université de Lyon,Service de Neurologie
[2] Université Claude Bernard,Centre de Recherche en Neurosciences de Lyon
[3] Hôpital Neurologique Pierre Wertheimer,Service de Neurologie
[4] Hospices Civils de Lyon,Service de Neurologie
[5] Observatoire Français de La Sclérose en Plaques,Service de Neurologie Et Centre d’Investigation Clinique
[6] EUGENE DEVIC EDMUS Foundation Against Multiple Sclerosis,Service de Neurologie
[7] State-Approved Foundation,Service de Neurologie
[8] CHU Nantes,Service de Neurologie
[9] INSERM,Institut de Génomique Fonctionnelle
[10] CIC 0004,Service de Neurologie
[11] CRTI-INSERM UMR U1064,Institut Toulousain Des Maladies Infectieuses Et Inflammatoires (Infinity)
[12] Centre Hospitalier Régional Et Universitaire de Nancy,Service de Neurologie
[13] Université de Lorraine,Service de Neurologie
[14] Aix Marseille University,Service de Neurologie
[15] APHM,Service de Neurologie
[16] Hôpital de La Timone,Service de Neurologie
[17] Pôle de Neurosciences Cliniques,Service de Neurologie
[18] Service de Neurologie,Pôle Des Neurosciences Et de L’appareil Locomoteur
[19] CEMEREM,Service de Neurologie
[20] CHU de Strasbourg,Service de Neurologie
[21] CHU de Montpellier,Département de Neurologie
[22] CHU de Bordeaux,Service de Neurologie
[23] Université de Bordeaux,Service de Neurologie
[24] INSERM,Service de Neurologie
[25] Neurocentre Magendie,Service de Neurologie
[26] CHU de Nîmes,Service de Neurologie
[27] Université de Montpellier,Service de Neurologie, Centre Expert SEP
[28] CNRS,Service de Neurologie
[29] INSERM,Service de Neurologie
[30] CHU de Toulouse,Service de Neurologie
[31] Hôpital Pierre-Paul Riquet,undefined
[32] CRC-SEP,undefined
[33] INSERM UMR 1291,undefined
[34] CNRS UMR 5051,undefined
[35] Université Toulouse III,undefined
[36] CHU de Besançon,undefined
[37] Hôpital Fondation A de Rothschild,undefined
[38] CHU de Clermont-Ferrand,undefined
[39] CHU Saint-Antoine,undefined
[40] CHU de Grenoble,undefined
[41] CHU de Rouen,undefined
[42] CRC-SEP,undefined
[43] Hôpital Roger Salengro,undefined
[44] Université de Lille,undefined
[45] CHU de Dijon,undefined
[46] Neurologie Pasteur 2,undefined
[47] CHU de Nice,undefined
[48] Université Nice Cote d’Azur UR2CA-URRIS,undefined
[49] APHP,undefined
[50] Hôpital Pitié-Salpêtrière,undefined
来源
Neurotherapeutics | 2022年 / 19卷
关键词
Multiple sclerosis; Fingolimod; Natalizumab; Anti-CD20; Therapeutics; Effectiveness; Flexible model;
D O I
暂无
中图分类号
学科分类号
摘要
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.
引用
收藏
页码:476 / 490
页数:14
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