TY - JOUR
T1 - Fingolimod vs dimethyl fumarate in multiple sclerosis
AU - Prosperini, Luca
AU - Lucchini, Matteo
AU - Haggiag, Shalom
AU - Bellantonio, Paolo
AU - Bianco, Assunta
AU - Buscarinu, Maria Chiara
AU - Buttari, Fabio
AU - Centonze, Diego
AU - Cortese, Antonio
AU - De Giglio, Laura
AU - Fantozzi, Roberta
AU - Ferraro, Elisabetta
AU - Fornasiero, Arianna
AU - Francia, Ada
AU - Galgani, Simonetta
AU - Gasperini, Claudio
AU - Marfia, Girolama Alessandra
AU - Millefiorini, Enrico
AU - Nociti, Viviana
AU - Pontecorvo, Simona
AU - Pozzilli, Carlo
AU - Ruggieri, Serena
AU - Salvetti, Marco
AU - Sgarlata, Eleonora
AU - Mirabella, Massimiliano
PY - 2018
Y1 - 2018
N2 - Objective To directly compare fingolimod (FNG) and dimethyl fumarate (DMF) on no evident disease activity (NEDA) status in patients with relapsing-remitting multiple sclerosis (RRMS) from 7 multiple sclerosis outpatient clinics in Central Italy.\r\n\r\nMethods We analyzed data of patients with RRMS who started an oral agent, namely DMF or FNG, either as first treatment (naives) or after switching from self-injectable drugs (switchers). We performed a propensity score (PS)–based nearest-neighbor matching within a caliper of 0.05 to select patients with homogeneous baseline characteristics. Pairwise censoring was adopted to adjust for difference in length of follow-up between the 2 treatment groups. Comparisons were then conducted in matched samples with Cox models (stratified by center) with NEDA-3 as the main outcome. NEDA-3 was defined as no relapses, no disability worsening, and no MRI activity.\r\n\r\nResults Overall, 483 and 456 patients eligible for analysis started on FNG and DMF, respectively. The PS-matching procedure retained a total of 550 patients (275 per group). After a median on-study follow-up of 18 months, the proportions of patients with NEDA-3 were similar (FNG 73%, DMF 70%; hazard ratio [HR] 0.74, p = 0.078). Subgroup analyses showed a comparable effectiveness of the 2 drugs in naives (n = 170, HR 1.15, p = 0.689), whereas FNG was superior to DMF in the achievement of NEDA-3 status among switchers (n = 380, HR 0.57, p = 0.007).\r\n\r\nConclusion We found no significant difference between FNG and DMF on NEDA-3 status, while subgroup analyses suggest the superiority of FNG over DMF in patients switching from self-injectable drugs.\r\n\r\nClassification of evidence This study provides Class IV evidence that for patients with RRMS, DMF and FNG have comparable efficacy in treatment-naive patients and that FNG is superior to DMF in patients switching from self-injectable drugs.
AB - Objective To directly compare fingolimod (FNG) and dimethyl fumarate (DMF) on no evident disease activity (NEDA) status in patients with relapsing-remitting multiple sclerosis (RRMS) from 7 multiple sclerosis outpatient clinics in Central Italy.\r\n\r\nMethods We analyzed data of patients with RRMS who started an oral agent, namely DMF or FNG, either as first treatment (naives) or after switching from self-injectable drugs (switchers). We performed a propensity score (PS)–based nearest-neighbor matching within a caliper of 0.05 to select patients with homogeneous baseline characteristics. Pairwise censoring was adopted to adjust for difference in length of follow-up between the 2 treatment groups. Comparisons were then conducted in matched samples with Cox models (stratified by center) with NEDA-3 as the main outcome. NEDA-3 was defined as no relapses, no disability worsening, and no MRI activity.\r\n\r\nResults Overall, 483 and 456 patients eligible for analysis started on FNG and DMF, respectively. The PS-matching procedure retained a total of 550 patients (275 per group). After a median on-study follow-up of 18 months, the proportions of patients with NEDA-3 were similar (FNG 73%, DMF 70%; hazard ratio [HR] 0.74, p = 0.078). Subgroup analyses showed a comparable effectiveness of the 2 drugs in naives (n = 170, HR 1.15, p = 0.689), whereas FNG was superior to DMF in the achievement of NEDA-3 status among switchers (n = 380, HR 0.57, p = 0.007).\r\n\r\nConclusion We found no significant difference between FNG and DMF on NEDA-3 status, while subgroup analyses suggest the superiority of FNG over DMF in patients switching from self-injectable drugs.\r\n\r\nClassification of evidence This study provides Class IV evidence that for patients with RRMS, DMF and FNG have comparable efficacy in treatment-naive patients and that FNG is superior to DMF in patients switching from self-injectable drugs.
KW - Multiple sclerosis
KW - case control)
KW - class IV
KW - clinical trials observational studies (Cohort
KW - Multiple sclerosis
KW - case control)
KW - class IV
KW - clinical trials observational studies (Cohort
UR - https://publicatt.unicatt.it/handle/10807/122008
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85057004194&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85057004194&origin=inward
U2 - 10.1212/WNL.0000000000005772
DO - 10.1212/WNL.0000000000005772
M3 - Article
SN - 0028-3878
VL - 2018
SP - 10.1212/WNL.0000000000005772-N/A/A
JO - Neurology
JF - Neurology
IS - June 6
ER -