Benefits of early highly effective versus escalation treatment strategies in relapsing multiple sclerosis estimated using a treatment-sequence model

Ide Smets*, Matthijs Versteegh, Simone Huygens, Beatrijs Wokke, Joost Smolders

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

2 Citations (Scopus)
25 Downloads (Pure)

Abstract

BACKGROUND: 

Uncertainty about disproportionate impact on health care budgets limits implementation of early highly effective treatment (EHT) in multiple sclerosis (MS).

OBJECTIVE: 

To estimate cost-effectiveness of escalation versus EHT disease-modifying treatment (DMT) sequences.

METHODS: 

Using a health-economic approach, we analysed health benefits (relapse rate reduction, disability prevention), direct/indirect DMT and societal costs of escalation versus EHT DMT sequences. In scenario analyses, we allowed (1) earlier use of alemtuzumab (ALE) and (2) a single retreatment with cladribine (CLA).

RESULTS: 

In our model, we showed that the ratio between costs and quality-adjusted life years (QALYs) for the most cost-effective EHT and escalation sequence results into a similar net health benefit with higher costs and also higher QALYs associated with an EHT versus escalation strategy. Earlier use of ALE is more cost-effective than in later lines, even when aggravating the impact of its side-effects tenfold. Retreatment with CLA was more cost-effective in both escalation and EHT sequences.

CONCLUSIONS: 

Certain EHT sequences are equally cost-effective to escalation sequences and are likely to result in more health at uncertain additional costs. The favourable cost-benefit ratio of CLA and ALE suggests that a wider application of affordable highly effective therapies could promote the cost-effectiveness both EHT and escalation approaches.

Original languageEnglish
Article number13524585241258692
Pages (from-to)1016-1025
Number of pages10
JournalMultiple Sclerosis Journal
Volume30
Issue number8
Early online date10 Jun 2024
DOIs
Publication statusPublished - Jun 2024

Bibliographical note

Publisher Copyright:
© The Author(s), 2024.

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