Comparative analysis of fingolimod versus teriflunomide in relapsing-remitting multiple sclerosis.


Journal

Multiple sclerosis and related disorders
ISSN: 2211-0356
Titre abrégé: Mult Scler Relat Disord
Pays: Netherlands
ID NLM: 101580247

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 17 01 2019
revised: 17 07 2019
accepted: 25 08 2019
pubmed: 2 9 2019
medline: 20 5 2020
entrez: 2 9 2019
Statut: ppublish

Résumé

Fingolimod and teriflunomide are commonly used in the treatment of relapsing-remitting multiple sclerosis (RRMS). These have not been compared in controlled trials, but only in observational studies, with inconclusive results. Comparison of their effect on relapse and disability in a real-world setting is therefore needed. The objective of this study was to compare the efficacy of fingolimod and teriflunomide in reducing disease activity in RRMS. This multicenter, retrospective observational study was carried out with prospectively collected data from 15 centers. All consecutive RRMS patients treated with teriflunomide or fingolimod were included. Data for relapses, Expanded Disability Status Scale (EDSS) scores and brain magnetic resonance imaging (MRI) scans were collected. Patients were matched using propensity scores. Annualized relapse rates (ARR), disability accumulation, percentage of patients with active MRI and treatment discontinuation over a median 2.5-year follow-up period were compared. Propensity score matching retained 349 out of 1388 patients in the fingolimod group and 349 out 678 in the teriflunomide group for final analyses. Mean ARR decreased markedly from baseline after 1 and 2 years of treatment in both the fingolimod (0.58-0.17 after 1 year and 0.11 after 2 years, p < 0.001) and teriflunomide (0.56-0.29 after 1 year and 0.31 after 2 years, p < 0.001) groups. Mean ARR was lower in fingolimod-treated patients than in those treated with teriflunomide at years 1 (p = 0.02) and 2 (p = 0.004). Compared to teriflunomide, the fingolimod group exhibited a higher percentage of relapse-free patients and a lower percentage of MRI-active patients after 2.5-year follow-up. Disability worsening was similar between the two groups. Patients were less likely to discontinue fingolimod than teriflunomide (p < 0.001). Fingolimod was associated with a better relapse control and lower discontinuation rate than teriflunomide. The two oral therapies exhibited similar effects on disability outcomes.

Sections du résumé

BACKGROUND BACKGROUND
Fingolimod and teriflunomide are commonly used in the treatment of relapsing-remitting multiple sclerosis (RRMS). These have not been compared in controlled trials, but only in observational studies, with inconclusive results. Comparison of their effect on relapse and disability in a real-world setting is therefore needed.
OBJECTIVES OBJECTIVE
The objective of this study was to compare the efficacy of fingolimod and teriflunomide in reducing disease activity in RRMS.
METHODS METHODS
This multicenter, retrospective observational study was carried out with prospectively collected data from 15 centers. All consecutive RRMS patients treated with teriflunomide or fingolimod were included. Data for relapses, Expanded Disability Status Scale (EDSS) scores and brain magnetic resonance imaging (MRI) scans were collected. Patients were matched using propensity scores. Annualized relapse rates (ARR), disability accumulation, percentage of patients with active MRI and treatment discontinuation over a median 2.5-year follow-up period were compared.
RESULTS RESULTS
Propensity score matching retained 349 out of 1388 patients in the fingolimod group and 349 out 678 in the teriflunomide group for final analyses. Mean ARR decreased markedly from baseline after 1 and 2 years of treatment in both the fingolimod (0.58-0.17 after 1 year and 0.11 after 2 years, p < 0.001) and teriflunomide (0.56-0.29 after 1 year and 0.31 after 2 years, p < 0.001) groups. Mean ARR was lower in fingolimod-treated patients than in those treated with teriflunomide at years 1 (p = 0.02) and 2 (p = 0.004). Compared to teriflunomide, the fingolimod group exhibited a higher percentage of relapse-free patients and a lower percentage of MRI-active patients after 2.5-year follow-up. Disability worsening was similar between the two groups. Patients were less likely to discontinue fingolimod than teriflunomide (p < 0.001).
CONCLUSION CONCLUSIONS
Fingolimod was associated with a better relapse control and lower discontinuation rate than teriflunomide. The two oral therapies exhibited similar effects on disability outcomes.

Identifiants

pubmed: 31473488
pii: S2211-0348(19)30353-0
doi: 10.1016/j.msard.2019.101376
pii:
doi:

Substances chimiques

Crotonates 0
Hydroxybutyrates 0
Immunologic Factors 0
Nitriles 0
Toluidines 0
teriflunomide 1C058IKG3B
Fingolimod Hydrochloride G926EC510T

Types de publication

Comparative Study Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

101376

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Cavit Boz (C)

Karadeniz Technical University, Department of Neurology, 61080, Trabzon, Turkey. Electronic address: cavitb@yahoo.com.

Murat Terzi (M)

Ondokuz Mayis University, Department of Neurology, Samsun, Turkey.

Bilge Özer (B)

Karadeniz Technical University, Department of Neurology, 61080, Trabzon, Turkey.

Recai Turkoglu (R)

Haydarpasa Numune Training and Research Hospital, Istanbul, Turkey.

Rana Karabudak (R)

Hacettepe University, Department of Neurology, Ankara, Turkey.

Hüsnü Efendi (H)

Kocaeli University, Department of Neurology, Izmit, Turkey.

Aysun Soysal (A)

Bakirkoy Education and Research Hospital for Psychiatric and Neurological Diseases, Istanbul, Turkey.

Serhan Sevim (S)

Mersin University, Department of Neurology, Mersin, Turkey.

Ayse Altintas (A)

Koc University, School of Medicine, Department of Neurology, Istanbul, Turkey.

Asli Kurne (A)

Hacettepe University, Department of Neurology, Ankara, Turkey.

Aylin Akçalı (A)

Gaziantep University, Department of Neurology, Gaziantep, Turkey.

Gülsen Akman (G)

Bilim University, Department of Neurology, Istanbul, Turkey.

Nur Yüceyar (N)

Ege University, Department of Neurology, Izmir, Turkey.

Belgin Petek Balcı (BP)

Department of Neurology, Haseki Educational and Research Center, Istanbul, Turkey.

Özgul Ekmekci (Ö)

Ege University, Department of Neurology, Izmir, Turkey.

Serap Zengin Karahan (SZ)

Karadeniz Technical University, Department of Neurology, 61080, Trabzon, Turkey.

Meltem Demirkıran (M)

Cukurova University, Department of Neurology, Adana, Turkey.

Burcu Altunrende (B)

Bilim University, Department of Neurology, Istanbul, Turkey.

Ömer Faruk Turan (ÖF)

Uludag University, Department of Neurology, Bursa, Turkey.
Bakirkoy Education and Research Hospital for Psychiatric and Neurological Diseases, Istanbul, Turkey.

Nilüfer Kale (N)

Bakirkoy Education and Research Hospital for Psychiatric and Neurological Diseases, Istanbul, Turkey.

Mesrure Köseoğlu (M)

Bakirkoy Education and Research Hospital for Psychiatric and Neurological Diseases, Istanbul, Turkey.

Serkan Ozakbas (S)

Dokuz Eylul University, Department of Neurology, Izmir, Turkey.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH