Cargando…

Quantifying the risk of disease reactivation after interferon and glatiramer acetate discontinuation in multiple sclerosis: The VIAADISC score

BACKGROUND AND PURPOSE: There is a lack of evidence guiding discontinuation of disease‐modifying therapy (DMT) in relapsing multiple sclerosis (RMS). Thus, the objective of this study was to generate and validate a risk score for disease reactivation after DMT discontinuation in RMS. METHODS: We dre...

Descripción completa

Detalles Bibliográficos
Autores principales: Bsteh, Gabriel, Hegen, Harald, Riedl, Katharina, Altmann, Patrick, Auer, Michael, Berek, Klaus, Di Pauli, Franziska, Ehling, Rainer, Kornek, Barbara, Monschein, Tobias, Rinner, Walter, Schmied, Christiane, Wurth, Sebastian, Zebenholzer, Karin, Zinganell, Anne, Zrzavy, Tobias, Zulehner, Gudrun, Deisenhammer, Florian, Rommer, Paulus, Leutmezer, Fritz, Berger, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248019/
https://www.ncbi.nlm.nih.gov/pubmed/33370478
http://dx.doi.org/10.1111/ene.14705
Descripción
Sumario:BACKGROUND AND PURPOSE: There is a lack of evidence guiding discontinuation of disease‐modifying therapy (DMT) in relapsing multiple sclerosis (RMS). Thus, the objective of this study was to generate and validate a risk score for disease reactivation after DMT discontinuation in RMS. METHODS: We drew a generation and validation dataset from two separate prospectively collected observational databases including RMS patients who received interferon‐β or glatiramer acetate for ≥12 months, then discontinued DMT for ≥6 months and had ≥2 years of follow‐up available. In the generation sample (n = 168), regression analysis was performed to identify clinical or magnetic resonance imaging (MRI) variables independently predicting disease reactivation after DMT discontinuation. A predictive score was calculated using the variables included in the multivariable model and applied to the validation sample (n = 98). RESULTS: The variables included in the final model as independent predictors of disease reactivation were age at discontinuation, MRI activity at discontinuation, and duration of clinical stability (all p < 0.001). The resulting score was able to robustly identify patients at high (83%–85%), moderate (36%–38%), and low risk (7%) of disease reactivation within 5 years after DMT discontinuation in both cohorts. CONCLUSIONS: The composite VIAADISC score is a valuable tool to inform and support patients and neurologists in the process of decision making to discontinue injectable DMTs.