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Comparative effectiveness of delayed-release dimethyl fumarate versus interferon, glatiramer acetate, teriflunomide, or fingolimod: results from the German NeuroTransData registry.
Braune, Stefan; Grimm, Sarah; van Hövell, Philip; Freudensprung, Ulrich; Pellegrini, Fabio; Hyde, Robert; Bergmann, Arnfin.
Afiliação
  • Braune S; NeuroTransData, Bahnhofstraße 103B, 86633, Neuburg an der Donau, Germany. braune@neurozentrum-prien.de.
  • Grimm S; PwC Digital Services, Birchstraße 160, 8050, Zurich, Switzerland.
  • van Hövell P; PwC Digital Services, Birchstraße 160, 8050, Zurich, Switzerland.
  • Freudensprung U; Biogen International GmbH, Landis Gyr-Straße 3, 6300, Zug, Switzerland.
  • Pellegrini F; Biogen International GmbH, Landis Gyr-Straße 3, 6300, Zug, Switzerland.
  • Hyde R; Biogen International GmbH, Landis Gyr-Straße 3, 6300, Zug, Switzerland.
  • Bergmann A; NeuroTransData, Bahnhofstraße 103B, 86633, Neuburg an der Donau, Germany.
J Neurol ; 265(12): 2980-2992, 2018 Dec.
Article em En | MEDLINE | ID: mdl-30327931
ABSTRACT

BACKGROUND:

Comparative effectiveness (CE) research allows real-world treatment comparisons using outcome measurements important to physicians/patients. This German NeuroTransData registry-based analysis compared delayed-release dimethyl fumarate (DMF) effectiveness with interferons (IFN), glatiramer acetate (GA), teriflunomide (TERI), or fingolimod (FTY) in patients with relapsing-remitting multiple sclerosis (RRMS) using propensity score matching (PSM).

METHODS:

Data from registry patients aged ≥ 18 years with RRMS, ≥ 1 relapse, and Expanded Disability Status Scale (EDSS) assessment(s) after index therapy initiation underwent 11 PSM to match DMF with comparator populations baseline characteristics. Primary outcome measurement was time to first relapse (TTFR). Secondary outcome measurements included annualised relapse rate (ARR), proportion of patients relapse free at 12 and 24 months, time to index therapy discontinuation (TTD), and reasons for discontinuation. Exploratory analyses included time to 3- and 6-month EDSS confirmed disability progression (CDP). Non-pairwise censoring was the primary analysis method; pairwise censoring was the main sensitivity analysis method.

FINDINGS:

Post-matched cohorts were well-balanced. By non-pairwise censoring, TTFR and ARR were significantly lower in DMF populations versus matched IFN, GA, and TERI, but there was no evidence of difference between DMF and FTY. TTD was similar between DMF and IFN, GA, and TERI, but significantly shorter versus FTY. Time to CDP generally showed no evidence of difference between DMF and comparator populations. Pairwise censored analysis results confirmed the non-pairwise censoring results.

INTERPRETATION:

These results support previous CE studies in demonstrating relative improvement in real-world effectiveness with DMF versus first-line agents IFN, GA, and TERI, and similar effectiveness versus FTY.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Toluidinas / Crotonatos / Interferons / Cloridrato de Fingolimode / Fumarato de Dimetilo / Acetato de Glatiramer / Fatores Imunológicos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male País/Região como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Toluidinas / Crotonatos / Interferons / Cloridrato de Fingolimode / Fumarato de Dimetilo / Acetato de Glatiramer / Fatores Imunológicos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male País/Região como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article