Fingolimod vs dimethyl fumarate in multiple sclerosis

  • Luca Prosperini*
  • , Matteo Lucchini
  • , Shalom Haggiag
  • , Paolo Bellantonio
  • , Assunta Bianco
  • , Maria Chiara Buscarinu
  • , Fabio Buttari
  • , Diego Centonze
  • , Antonio Cortese
  • , Laura De Giglio
  • , Roberta Fantozzi
  • , Elisabetta Ferraro
  • , Arianna Fornasiero
  • , Ada Francia
  • , Simonetta Galgani
  • , Claudio Gasperini
  • , Girolama Alessandra Marfia
  • , Enrico Millefiorini
  • , Viviana Nociti
  • , Simona Pontecorvo
  • Carlo Pozzilli, Serena Ruggieri, Marco Salvetti, Eleonora Sgarlata, Massimiliano Mirabella
*Autore corrispondente per questo lavoro

Risultato della ricerca: Contributo in rivistaArticolopeer review

Abstract

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.
Lingua originaleInglese
pagine (da-a)10.1212/WNL.0000000000005772-N/A/A
RivistaNeurology
Volume2018
Numero di pubblicazioneJune 6
DOI
Stato di pubblicazionePubblicato - 2018

All Science Journal Classification (ASJC) codes

  • Neurologia (clinica)

Keywords

  • Multiple sclerosis
  • case control)
  • class IV
  • clinical trials observational studies (Cohort

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