Natalizumab wearing-off symptoms: effect of extend interval dosing during Sars-CoV-2 pandemic.


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 08 07 2022
accepted: 27 09 2022
revised: 26 09 2022
pubmed: 14 10 2022
medline: 2 2 2023
entrez: 13 10 2022
Statut: ppublish

Résumé

Many patients treated with Natalizumab experience wearing-off symptoms (WoS) towards the end of the administration cycle. During the pandemic we advised and asked patients undergoing treatment with Natalizumab if they wanted to be shifted from a standard interval dosing (StID of 4 weeks) to an extended interval dosing (ExID of 5-6 weeks), regardless of their JCV index. Our main objective was to study prevalence and incidence of WoS when ExID was adopted. We enrolled 86 patients, from May 2020 to January 2021, evaluated at baseline and during a 6 months follow-up with a survey focused on WoS, Fatigue Severity Scale (FSS), Expanded Disability Status Scale (EDSS) and MRI. Among the 86 patients, 32 (37.2%) reported WoS. Most common one was fatigue (93.7%). Mean EDSS was higher in the group reporting WoS (3.8 WoS vs 3.1 non-WoS, p < 0.05). Sphincterial function was the EDSS item that significantly differed between the WoS group and the non-WoS group (1.4 WoS vs 0.6 non-WoS, p < 0.001). WoS correlate with the FSS scale (p < 0.001). Adopting an extended interval dosing does not result in significantly different occurrence of WoS between the ExID and the StID populations, in our cohort of patients. Interestingly, there is a strong correlation between WoS and a higher EDSS and FSS. Safety and efficacy of Natalizumab with ExID are relatively preserved in our study.

Sections du résumé

BACKGROUND BACKGROUND
Many patients treated with Natalizumab experience wearing-off symptoms (WoS) towards the end of the administration cycle. During the pandemic we advised and asked patients undergoing treatment with Natalizumab if they wanted to be shifted from a standard interval dosing (StID of 4 weeks) to an extended interval dosing (ExID of 5-6 weeks), regardless of their JCV index. Our main objective was to study prevalence and incidence of WoS when ExID was adopted.
METHODS METHODS
We enrolled 86 patients, from May 2020 to January 2021, evaluated at baseline and during a 6 months follow-up with a survey focused on WoS, Fatigue Severity Scale (FSS), Expanded Disability Status Scale (EDSS) and MRI.
RESULTS RESULTS
Among the 86 patients, 32 (37.2%) reported WoS. Most common one was fatigue (93.7%). Mean EDSS was higher in the group reporting WoS (3.8 WoS vs 3.1 non-WoS, p < 0.05). Sphincterial function was the EDSS item that significantly differed between the WoS group and the non-WoS group (1.4 WoS vs 0.6 non-WoS, p < 0.001). WoS correlate with the FSS scale (p < 0.001).
CONCLUSION CONCLUSIONS
Adopting an extended interval dosing does not result in significantly different occurrence of WoS between the ExID and the StID populations, in our cohort of patients. Interestingly, there is a strong correlation between WoS and a higher EDSS and FSS. Safety and efficacy of Natalizumab with ExID are relatively preserved in our study.

Identifiants

pubmed: 36229702
doi: 10.1007/s00415-022-11408-0
pii: 10.1007/s00415-022-11408-0
pmc: PMC9559546
doi:

Substances chimiques

Natalizumab 0
Immunologic Factors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

595-600

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.

Références

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Auteurs

Giuseppe Magro (G)

Institute of Neurology, University Magna Graecia of Catanzaro, Viale Europa, Germaneto, 88100, Catanzaro, CZ, Italy.

Stefania Barone (S)

Institute of Neurology, University Magna Graecia of Catanzaro, Viale Europa, Germaneto, 88100, Catanzaro, CZ, Italy.

Federico Tosto (F)

Institute of Neurology, University Magna Graecia of Catanzaro, Viale Europa, Germaneto, 88100, Catanzaro, CZ, Italy.

Antonio De Martino (A)

Institute of Neurology, University Magna Graecia of Catanzaro, Viale Europa, Germaneto, 88100, Catanzaro, CZ, Italy.

Domenico Santange Lo (D)

Institute of Neurology, University Magna Graecia of Catanzaro, Viale Europa, Germaneto, 88100, Catanzaro, CZ, Italy.

Lucia Manzo (L)

Institute of Neurology, University Magna Graecia of Catanzaro, Viale Europa, Germaneto, 88100, Catanzaro, CZ, Italy.

Angelo Pascarella (A)

Institute of Neurology, University Magna Graecia of Catanzaro, Viale Europa, Germaneto, 88100, Catanzaro, CZ, Italy.

Pietro Bruno (P)

Institute of Neurology, University Magna Graecia of Catanzaro, Viale Europa, Germaneto, 88100, Catanzaro, CZ, Italy.

Marilisa Pasquale (M)

Institute of Neurology, University Magna Graecia of Catanzaro, Viale Europa, Germaneto, 88100, Catanzaro, CZ, Italy.

Antonio Gambardella (A)

Institute of Neurology, University Magna Graecia of Catanzaro, Viale Europa, Germaneto, 88100, Catanzaro, CZ, Italy.

Paola Valentino (P)

Institute of Neurology, University Magna Graecia of Catanzaro, Viale Europa, Germaneto, 88100, Catanzaro, CZ, Italy. p.vale@unicz.it.

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