Modified Rio Score with Platform Therapy Predicts Treatment Success with Fingolimod and Natalizumab in Relapsing-Remitting Multiple Sclerosis Patients.

fingolimod modified Rio score (MRS) natalizumab no evidence of disease activity (NEDA) relapsing-remitting type of multiple sclerosis

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
22 Apr 2021
Historique:
received: 03 03 2021
revised: 12 04 2021
accepted: 20 04 2021
entrez: 30 4 2021
pubmed: 1 5 2021
medline: 1 5 2021
Statut: epublish

Résumé

Reliable markers of disease outcomes in multiple sclerosis (MS) would help to predict the response to treatment in patients treated with high efficacy drugs. No evidence of disease activity (NEDA) has become a treatment goal whereas the modified Rio score (MRS) predicts future suboptimal responders to treatment. The aim of our study was to identify factors that would predict poor response to treatment with natalizumab and fingolimod. In the multicenter prospective trial, 336 subjects were enrolled, initiating therapy with natalizumab ( NEDA-3 after the first year of therapy was 73.9% for natalizumab and 54.8% for fingolimod ( We conclude that switching to the second-line therapy should occur earlier to enable better results for patients treated with natalizumab or fingolimod. The outcome on both drugs is better with better neurological conditions and lower MRS of the patient on the platform therapy.

Sections du résumé

BACKGROUND BACKGROUND
Reliable markers of disease outcomes in multiple sclerosis (MS) would help to predict the response to treatment in patients treated with high efficacy drugs. No evidence of disease activity (NEDA) has become a treatment goal whereas the modified Rio score (MRS) predicts future suboptimal responders to treatment. The aim of our study was to identify factors that would predict poor response to treatment with natalizumab and fingolimod.
METHODS METHODS
In the multicenter prospective trial, 336 subjects were enrolled, initiating therapy with natalizumab (
RESULTS RESULTS
NEDA-3 after the first year of therapy was 73.9% for natalizumab and 54.8% for fingolimod (
CONCLUSION CONCLUSIONS
We conclude that switching to the second-line therapy should occur earlier to enable better results for patients treated with natalizumab or fingolimod. The outcome on both drugs is better with better neurological conditions and lower MRS of the patient on the platform therapy.

Identifiants

pubmed: 33922368
pii: jcm10091830
doi: 10.3390/jcm10091830
pmc: PMC8122749
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Anna Jamroz-Wiśniewska (A)

Department of Neurology, Medical University of Lublin, Jaczewskiego 8, 20-054 Lublin, Poland.

Radosław Zajdel (R)

Chair of Informatics in Business, University of Lodz, Rewolucji 1905 Roku 37/39, 91-001 Lodz, Poland.

Agnieszka Słowik (A)

Department of Neurology, Collegium Medicum, Jagiellonian University, Jakubowskiego 2, 30-688 Krakow, Poland.

Monika Marona (M)

Department of Neurology, Collegium Medicum, Jagiellonian University, Jakubowskiego 2, 30-688 Krakow, Poland.

Marcin Wnuk (M)

Department of Neurology, Collegium Medicum, Jagiellonian University, Jakubowskiego 2, 30-688 Krakow, Poland.

Monika Adamczyk-Sowa (M)

Department of Neurology, School of Health Sciences in Zabrze, Medical University of Silesia in Katowice, 3-go Maja 13-15, 41-800 Zabrze, Poland.

Bożena Adamczyk (B)

Department of Neurology, School of Health Sciences in Zabrze, Medical University of Silesia in Katowice, 3-go Maja 13-15, 41-800 Zabrze, Poland.

Anetta Lasek-Bal (A)

Department of Neurology, School of Health Sciences, Medical University of Silesia in Katowice, Ziolowa 45-47, 40-635 Katowice, Poland.

Przemysław Puz (P)

Department of Neurology, School of Health Sciences, Medical University of Silesia in Katowice, Ziolowa 45-47, 40-635 Katowice, Poland.

Arkadiusz Stęposz (A)

Department of Neurology, School of Health Sciences, Medical University of Silesia in Katowice, Ziolowa 45-47, 40-635 Katowice, Poland.

Ewa Krzystanek (E)

Department of Neurology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 14, 40-752 Katowice, Poland.

Maja Patalong-Ogiewa (M)

Department of Neurorehabilitation, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 14, 40-752 Katowice, Poland.

Anna Pokryszko-Dragan (A)

Department of Neurology, Wroclaw Medical University, Borowska 213, 50-566 Wroclaw, Poland.

Sławomir Budrewicz (S)

Department of Neurology, Wroclaw Medical University, Borowska 213, 50-566 Wroclaw, Poland.

Dorota Koziarska (D)

Department of Neurology, Pomeranian Medical University in Szczecin, Unii Lubelskiej 1, 71-252 Szczecin, Poland.

Anna Karbicka (A)

Department of Neurology, Regional Hospital, Arkonska 4, 71-455 Szczecin, Poland.

Sławomir Wawrzyniak (S)

Department of Neurology, 10th Military Research Hospital and Polyclinic, Powstancow Warszawy 5, 85-681 Bydgoszcz, Poland.

Waldemar Fryze (W)

Department of Neurology, Copernicus Pl, M. Kopernik Hospital, Nowe Ogrody 1-6, 80-803 Gdansk, Poland.

Marzena Furtak-Niczyporuk (M)

Department of Public Health, Medical University of Lublin, 20-954 Lublin, Poland.

Konrad Rejdak (K)

Department of Neurology, Medical University of Lublin, Jaczewskiego 8, 20-054 Lublin, Poland.

Classifications MeSH