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Real-world effectiveness of natalizumab and fingolimod compared with self-injectable drugs in non-responders and in treatment-naïve patients with multiple sclerosis

  • Luca Prosperini*
  • , Francesco Saccà
  • , Cinzia Cordioli
  • , Antonio Cortese
  • , Fabio Buttari
  • , Simona Pontecorvo
  • , Assunta Bianco
  • , Serena Ruggieri
  • , Shalom Haggiag
  • , Vincenzo Brescia Morra
  • , Ruggero Capra
  • , Diego Centonze
  • , Giancarlo Di Battista
  • , Elisabetta Ferraro
  • , Ada Francia
  • , Simonetta Galgani
  • , Claudio Gasperini
  • , Enrico Millefiorini
  • , Massimiliano Mirabella
  • , Carlo Pozzilli
  • *Autore corrispondente per questo lavoro
  • Sapienza University of Rome
  • University of Naples Federico II
  • Spedali Civili Di Brescia
  • IRCCS Istituto Neurologico Mediterraneo Neuromed - Pozzilli (IS)
  • University of Rome Tor Vergata
  • San Camillo Hospital
  • San Filippo Neri Hospital
  • Sant'Andrea Hospital

Risultato della ricerca: Contributo in rivista › Articolo

Abstract

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.
Lingua originaleInglese
pagine (da-a)284-294
Numero di pagine11
RivistaJournal of Neurology
Volume264
Numero di pubblicazione2
DOI
Stato di pubblicazionePubblicato - 2017

All Science Journal Classification (ASJC) codes

  • Neurologia
  • Neurologia (clinica)

Keywords

  • Disease-modifying drugs
  • Multiple sclerosis
  • NEDA
  • Neurology
  • Neurology (clinical)
  • Propensity score

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