10-YEAR COST-EFFECTIVENESS ANALYSES OF RESPONSE-BASED USE OF FREMANEZUMAB AS PREVENTIVE TREATMENT IN CHRONIC AND EPISODIC MIGRAINE FOR PATIENTS WITH INADEQUATE RESPONSE TO PRIOR PREVENTIVE TREATMENTS

Author(s)

Smolen L1, Thompson S2, Klein T1, Cohen J2, Gandhi SK2
1Medical Decision Modeling Inc., Indianapolis, IN, USA, 2Teva Pharmaceuticals, Frazer, PA, USA

OBJECTIVES: The cost-effectiveness of fremanezumab for preventive treatment of chronic (CM) and episodic migraine (EM) in patients who had responded inadequately to 2 to 4 classes of prior preventive treatments was examined, accounting for cessation of fremanezumab treatment for non-responding patients.

METHODS: A semi-Markov cost-effectiveness model (CEM) was developed with a 4-week cycle and 10-year analysis time horizon. Costs and benefits were discounted at 3.0% annual rates. Treatment efficacy was incorporated as reduction in mean migraine days(MDs)/28days versus placebo. Patient cohorts were distributed among MD categories (0–28MDs/28days) based on mean MD levels. The CEM-estimated costs (fremanezumab acquisition and MD-related costs) and health-related-quality-of-life (MD- and treatment status–based utilities) for fremanezumab and no-treatment arms. Only background mortality was modeled. Analyses were performed on a combined CM(67%)/EM(33%) population. CM/EM patients not achieving 30%/50% reductions, respectively, in MDs/28days at 12 weeks(non-responders) stopped fremanezumab treatment. The incremental cost-effectiveness ratio (ICER) was reported as cost/quality-adjusted life-year (QALY) gained between fremanezumab and no treatment. Fremanezumab MDs/28day reductions versus placebo and 12-week non-response rates were sourced from a network meta-analysis. In the base-case analysis, fremanezumab was compared with constant no-treatment MD profiles. Fremanezumab was also compared with randomized-controlled trial (RCT)-sourced placebo-arm MD profiles.

RESULTS: In base-case, 10-year analysis time horizon, fremanezumab treatment dominates no treatment (less costly, more effective): average cost savings, $3,492/patient; incremental QALYs, 0.22; and reduction in MDs, 161.5MDs. Excluding indirect costs, fremanezumab treatment resulted in a cost/QALY ICER of $13,606, with average incremental costs of $2,998/patient. When placebo effects were included, fremanezumab treatment dominates no treatment (less costly, more effective): average cost savings, $13,905/patient; incremental QALYs, 0.412; and reduction in MDs, 353.9MDs.

CONCLUSIONS: Based on current pricing and RCT results, fremanezumab treatment is cost-effective versus no treatment, especially if treatment is discontinued at 12 weeks for non-responders, as defined in the analysis.

Conference/Value in Health Info

2019-11, ISPOR Europe 2019, Copenhagen, Denmark

Code

PND37

Topic

Economic Evaluation

Disease

Neurological Disorders

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