Modeling the Cost-Utility of Treatment Sequences for Multiple Sclerosis

Simone Huygens*, Matthijs Versteegh

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

3 Citations (Scopus)
2 Downloads (Pure)

Abstract

Objectives: Most patients with multiple sclerosis (MS) switch between disease-modifying therapies (DMTs) during their lifetime. Our aim was to develop an MS cost-utility model that takes treatment switching into account to provide a more realistic estimate of treatment benefit than previous models that assume lifetime use of 1 DMT. Methods: A treatment sequence model using a microsimulation framework with a lifetime time horizon and a societal perspective was developed in R. Clinical plausibility and decision rules for switching were defined in consultation with Dutch MS neurologists. The ability of DMTs to prevent relapses and delay disease progression was modeled by applying DMT-specific estimates derived from a network meta-analysis of randomized controlled trials to natural history data. A total of 2 treatment strategies were compared: a first-line DMT sequence (peginterferon-glatiramer-teriflunomide-interferon-beta-dimethyl fumarate) and an escalation DMT sequence (peginterferon-glatiramer-ocrelizumab-natalizumab-alemtuzumab). Scenario analyses explored impact of alternative sources of natural history data, societal versus healthcare perspective, and condition-specific versus generic utilities. Predicted short-term switches (<5 years) were externally validated with Dutch claims data on DMT use. Results: Short-term switches predicted by the model compared well with Dutch claims data. Transition from relapsing-remitting MS to secondary progressive MS was delayed by the escalation sequence (24.7 vs 20.3 years on first-line sequence). Model results were sensitive to utility values and medical resource consumption was a large driver of uncertainty. Conclusions: This microsimulation model overcomes the limitation of previous models by modeling treatment sequences. Because it better reflects clinical reality, it facilitates incorporating cost-utility information in clinical guidelines.

Original languageEnglish
Pages (from-to)1612-1619
Number of pages8
JournalValue in Health
Volume24
Issue number11
Early online date10 Aug 2021
DOIs
Publication statusPublished - 1 Nov 2021

Bibliographical note

Funding Information:
Conflict of Interest Disclosures: Drs Huygens and Versteegh reported receiving an unrestricted research grant from Erasmus University Medical Center. The funding agreement ensured the authors’ independence in designing the study, interpreting the data, writing, and publishing the report. Drs Huygens and Versteegh are employed by the Institute for Medical Technology Assessment, which received payments for activities related to patient preferences in multiple sclerosis from EMD-Serono and Merck KgGA outside the submitted work.

Publisher Copyright:
© 2021 ISPOR–The Professional Society for Health Economics and Outcomes Research

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