Benefits of sphingosine-1-phosphate receptor modulators in relapsing MS estimated with a treatment sequence model

被引:1
作者
Corsten, Cato E. A. [1 ]
Huygens, Simone A. [3 ]
Versteegh, Matthijs M. [3 ]
Wokke, Beatrijs H. A. [1 ]
Smets, Ide [1 ]
Smolders, Joost [1 ,2 ]
机构
[1] Erasmus MC, MS Ctr ErasMS, Dept Neurol, Doctor Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands
[2] Erasmus MC, Dept Immunol, Doctor Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands
[3] Huygens & Versteegh, Zwijndrecht, Netherlands
关键词
Relapsing remitting multiple sclerosis; Disease-modifying therapy; Treatment sequence; Sphingosine-1-phosphate receptor modulators; Health economics; Cost-effectiveness; MULTIPLE-SCLEROSIS; ORAL FINGOLIMOD; COST-UTILITY; DOUBLE-BLIND; BURDEN; INSIGHTS; PHASE-3; DISEASE;
D O I
10.1016/j.msard.2023.105100
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Three sphingosine-1-phosphate receptor (S1PR) modulators are currently available as disease-modifying therapies (DMTs) for relapsing MS in the Netherlands (i.e. fingolimod, ozanimod and ponesimod). We aimed to identify which S1PR modulator yields the highest benefit from a health-economic and societal perspective during a patient's lifespan. Methods: Incorporating Dutch DMT list prices, we used the ErasmusMC/iMTA MS model to compare DMT sequences, including S1PR modulators and eight other DMT classes, for treatment-naive patients with relapsing MS in terms of health outcomes (number of lifetime relapses, time to Expanded Disability Status Scale (EDSS) 6, lifetime quality-adjusted life years (QALYs)) and cost-effectiveness (net health benefit (NHB)). We estimated the influence of list price and EDSS progression on cost-effectiveness outcomes. Results: In deterministic and probabilistic analysis, DMT sequences with ponesimod have lower lifetime costs and higher QALYs resulting in a higher average NHB compared to sequences with other S1PR modulators. Ponesimod remains the most cost-effective S1PR modulator when EDSS progression is class-averaged. Given the variable effects on disability progression, list price reductions could make fingolimod but not ozanimod more cost-effective than ponesimod. Conclusion: Our model favours ponesimod among the S1PR modulators for the treatment of relapsing MS. This implies that prioritizing ponesimod over other S1PR modulators translates into a more efficacious spending of national healthcare budget without reducing benefit for people with MS. Prioritizing cost-effective choices when counselling patients contributes to affordable and accessible MS care.
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