Literature DB >> 33370478

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

Gabriel Bsteh1, Harald Hegen2, Katharina Riedl1, Patrick Altmann1, Michael Auer2, Klaus Berek2, Franziska Di Pauli2, Rainer Ehling3, Barbara Kornek1, Tobias Monschein1, Walter Rinner1, Christiane Schmied1, Sebastian Wurth4, Karin Zebenholzer1, Anne Zinganell2, Tobias Zrzavy1, Gudrun Zulehner1, Florian Deisenhammer2, Paulus Rommer1, Fritz Leutmezer1, Thomas Berger1.   

Abstract

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.
© 2020 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.

Entities:  

Keywords:  discontinuation; disease-modifying therapy; multiple sclerosis; reactivation; risk AUTHOR: Please check the list of abbreviations.

Year:  2021        PMID: 33370478     DOI: 10.1111/ene.14705

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  5 in total

1.  Peripheral Hemolysis in Relation to Iron Rim Presence and Brain Volume in Multiple Sclerosis.

Authors:  Nik Krajnc; Gabriel Bsteh; Gregor Kasprian; Tobias Zrzavy; Barbara Kornek; Thomas Berger; Fritz Leutmezer; Paulus Rommer; Hans Lassmann; Simon Hametner; Assunta Dal-Bianco
Journal:  Front Neurol       Date:  2022-06-29       Impact factor: 4.086

2.  Has the pandemic changed treatment strategy in multiple sclerosis?

Authors:  Gabriel Bsteh; Katharina Riedl; Nik Krajnc; Barbara Kornek; Fritz Leutmezer; Stefan Macher; Paulus Rommer; Gudrun Zulehner; Thomas Berger
Journal:  Mult Scler Relat Disord       Date:  2022-05-23       Impact factor: 4.808

3.  Evolution of Disease Modifying Therapy Benefits and Risks: An Argument for De-escalation as a Treatment Paradigm for Patients With Multiple Sclerosis.

Authors:  Brandi L Vollmer; Andrew B Wolf; Stefan Sillau; John R Corboy; Enrique Alvarez
Journal:  Front Neurol       Date:  2022-01-25       Impact factor: 4.003

Review 4.  Treatment Challenges in Multiple Sclerosis - A Continued Role for Glatiramer Acetate?

Authors:  Massimiliano Mirabella; Pietro Annovazzi; Wallace Brownlee; Jeffrey A Cohen; Christoph Kleinschnitz; Christian Wolf
Journal:  Front Neurol       Date:  2022-04-15       Impact factor: 4.086

5.  Estimating Risk of Multiple Sclerosis Disease Reactivation in Pregnancy and Postpartum: The VIPRiMS Score.

Authors:  Gabriel Bsteh; Harald Hegen; Katharina Riedl; Patrick Altmann; Franziska Di Pauli; Rainer Ehling; Gudrun Zulehner; Paulus Rommer; Fritz Leutmezer; Florian Deisenhammer; Thomas Berger
Journal:  Front Neurol       Date:  2022-01-17       Impact factor: 4.003

  5 in total

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