TY - JOUR
T1 - Effectiveness of teriflunomide on No Evidence of Disease Activity and cognition in relapsing remitting multiple sclerosis
T2 - results of the NEDA3PLUS study
AU - Amato, Maria Pia
AU - Bergamaschi, Roberto
AU - Centonze, Diego
AU - Mirabella, Massimiliano
AU - Marfia, Girolama Alessandra
AU - Totaro, Rocco
AU - Lus, Giacomo
AU - Brescia Morra, Vincenzo
AU - Aguglia, Umberto
AU - Comi, Cristoforo
AU - Cavalla, Paola
AU - Zaffaroni, Mauro
AU - Rovaris, Marco
AU - Grimaldi, Luigi Maria
AU - Leoni, Stefania
AU - Malucchi, Simona
AU - Baldi, Eleonora
AU - Romano, Marcello
AU - Falcini, Mario
AU - Perini, Paola
AU - Assetta, Maurizio
AU - Portaccio, Emilio
AU - Sommacal, Sergio
AU - Olivieri, Nunzio
AU - Parodi, Franco
AU - Todaro, Daniele Santo
AU - Grassivaro, Nicoletta
AU - Farina, Alberto
AU - Mondino, Margaret Mary
AU - Filippi, Massimo
AU - Trojano, Maria
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/10
Y1 - 2023/10
N2 - 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.
AB - 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.
KW - Cognition
KW - Multiple sclerosis
KW - No Evidence of Disease Activity
KW - Observational
KW - Teriflunomide
UR - http://www.scopus.com/inward/record.url?scp=85164112937&partnerID=8YFLogxK
U2 - 10.1007/s00415-023-11820-0
DO - 10.1007/s00415-023-11820-0
M3 - Article
SN - 0340-5354
VL - 270
SP - 4687
EP - 4696
JO - Journal of Neurology
JF - Journal of Neurology
IS - 10
ER -