TY - JOUR
T1 - Real-world effectiveness of natalizumab and fingolimod compared with self-injectable drugs in non-responders and in treatment-naïve patients with multiple sclerosis
AU - Prosperini, Luca
AU - Saccà, Francesco
AU - Cordioli, Cinzia
AU - Cortese, Antonio
AU - Buttari, Fabio
AU - Pontecorvo, Simona
AU - Bianco, Assunta
AU - Ruggieri, Serena
AU - Haggiag, Shalom
AU - Brescia Morra, Vincenzo
AU - Capra, Ruggero
AU - Centonze, Diego
AU - Di Battista, Giancarlo
AU - Ferraro, Elisabetta
AU - Francia, Ada
AU - Galgani, Simonetta
AU - Gasperini, Claudio
AU - Millefiorini, Enrico
AU - Mirabella, Massimiliano
AU - Pozzilli, Carlo
PY - 2017
Y1 - 2017
N2 - In this independent, multicentre post-marketing study we directly compared the effectiveness of natalizumab (NTZ), fingolimod (FNG) and self-injectable drugs (INJ), in non-responders to first immunomodulating treatment and in highly active treatment-naïve patients with multiple sclerosis. As main outcome measure we considered the proportions of patients with no evidence of disease activity (NEDA-3), defined as absence of relapses, disability worsening and radiological activity. A total of 567 non-responders to interferon beta (IFNB) or glatiramer acetate (GA) [dataset A] and 216 highly active treatment-naïves [dataset B] were followed up to 24 months from the beginning of NTZ, FNG or INJ, i.e. switching from IFNB to GA or viceversa (in the case of non-responders) or starting high-dose IFNB (in the case of highly active treatment-naïves). Propensity score matching in a 1:1:1 ratio was used to select only patients with similar baseline characteristics, retaining 330 and 120 patients in dataset A and B, respectively. In dataset A, the 24-month proportion with NEDA-3 was greater in both NTZ group (67%) and FNG group (42%) than in INJ group (35%) (p ≤ 0.016); however, NTZ was superior to FNG in promoting the attainment of NEDA-3 status (p = 0.034). In dataset B, the 24-month proportion with NEDA-3 was greater in NTZ group (75%) and FNG group (67%) than in INJ group (40%), but the small cohort sizes most likely prevented the detection of any statistically significant difference. Our study provides real-world evidence that NTZ was more effective than both FNG and INJ in non-responders, while it could seem that, in highly active treatment-naïves, NTZ was as effective as FNG and both were superior to INJ.
AB - In this independent, multicentre post-marketing study we directly compared the effectiveness of natalizumab (NTZ), fingolimod (FNG) and self-injectable drugs (INJ), in non-responders to first immunomodulating treatment and in highly active treatment-naïve patients with multiple sclerosis. As main outcome measure we considered the proportions of patients with no evidence of disease activity (NEDA-3), defined as absence of relapses, disability worsening and radiological activity. A total of 567 non-responders to interferon beta (IFNB) or glatiramer acetate (GA) [dataset A] and 216 highly active treatment-naïves [dataset B] were followed up to 24 months from the beginning of NTZ, FNG or INJ, i.e. switching from IFNB to GA or viceversa (in the case of non-responders) or starting high-dose IFNB (in the case of highly active treatment-naïves). Propensity score matching in a 1:1:1 ratio was used to select only patients with similar baseline characteristics, retaining 330 and 120 patients in dataset A and B, respectively. In dataset A, the 24-month proportion with NEDA-3 was greater in both NTZ group (67%) and FNG group (42%) than in INJ group (35%) (p ≤ 0.016); however, NTZ was superior to FNG in promoting the attainment of NEDA-3 status (p = 0.034). In dataset B, the 24-month proportion with NEDA-3 was greater in NTZ group (75%) and FNG group (67%) than in INJ group (40%), but the small cohort sizes most likely prevented the detection of any statistically significant difference. Our study provides real-world evidence that NTZ was more effective than both FNG and INJ in non-responders, while it could seem that, in highly active treatment-naïves, NTZ was as effective as FNG and both were superior to INJ.
KW - Disease-modifying drugs
KW - Multiple sclerosis
KW - NEDA
KW - Neurology
KW - Neurology (clinical)
KW - Propensity score
KW - Disease-modifying drugs
KW - Multiple sclerosis
KW - NEDA
KW - Neurology
KW - Neurology (clinical)
KW - Propensity score
UR - http://hdl.handle.net/10807/96123
U2 - 10.1007/s00415-016-8343-5
DO - 10.1007/s00415-016-8343-5
M3 - Article
SN - 0340-5354
VL - 264
SP - 284
EP - 294
JO - Journal of Neurology
JF - Journal of Neurology
ER -