Effectiveness of teriflunomide on No Evidence of Disease Activity and cognition in relapsing remitting multiple sclerosis: results of the NEDA3PLUS study

  • Maria Pia Amato
  • , Roberto Bergamaschi
  • , Diego Centonze
  • , Massimiliano Mirabella
  • , Girolama Alessandra Marfia
  • , Rocco Totaro
  • , Giacomo Lus
  • , Vincenzo Brescia Morra
  • , Umberto Aguglia
  • , Cristoforo Comi
  • , Paola Cavalla
  • , Mauro Zaffaroni
  • , Marco Rovaris
  • , Luigi Maria Grimaldi
  • , Stefania Leoni
  • , Simona Malucchi
  • , Eleonora Baldi
  • , Marcello Romano
  • , Mario Falcini
  • , Paola Perini
  • Maurizio Assetta, Emilio Portaccio, Sergio Sommacal, Nunzio Olivieri, Franco Parodi, Daniele Santo Todaro, Nicoletta Grassivaro, Alberto Farina, Margaret Mary Mondino, Massimo Filippi, Maria Trojano

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

Background: Cognitive impairment (CI) is a prevalent and debilitating manifestation of multiple sclerosis (MS); however, it is not included in the widely used concept of No Evidence of Disease Activity (NEDA-3). We expanded the NEDA-3 concept to NEDA-3 + by encompassing CI assessed through the Symbol Digit Modality Test (SDMT) and evaluated the effect of teriflunomide on NEDA3 + in patients treated in a real-world setting. The value of NEDA-3 + in predicting disability progression was also assessed. Methods: This 96-weeks observational study enrolled patients already on treatment with teriflunomide for ≥ 24 weeks. The predictiveness of NEDA-3 and NEDA-3 + at 48 weeks on the change in motor disability at 96 weeks was compared through a two-sided McNemar test. Results: The full analysis set (n = 128; 38% treatment naïve) featured relatively low level of disability (baseline EDSS = 1.97 ± 1.33). NEDA-3 and NEDA-3 + statuses were achieved by 82.8% and 64.8% of patients, respectively at 48 weeks vs. baseline, and by 57.0% and 49.2% of patients, respectively at 96 weeks vs. baseline. All patients except one were free of disability progression at Week 96, and NEDA-3 and NEDA-3 + were equally predictive. Most patients were free of relapse (87.5%), disability progression (94.5%) and new MRI activity (67.2%) comparing 96 weeks with baseline. SDMT scores were stable in patients with baseline score ˃35 and improved significantly in those with baseline score ≤ 35. Treatment persistence was high (81.0% at Week 96). Conclusion: Teriflunomide confirmed its real-world efficacy and was found to have a potentially beneficial effect on cognition.

Lingua originaleInglese
pagine (da-a)4687-4696
Numero di pagine10
RivistaJournal of Neurology
Volume270
Numero di pubblicazione10
DOI
Stato di pubblicazionePubblicato - ott 2023

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