Abstract

ObjectiveTo study cost-effectiveness of an interleukin (IL)-17A inhibitor secukinumab, with other biologics and apremilast in patients with Psoriatic arthritis (PsA) from payer perspective in Finland.MethodsIn this semi-Markov model, subcutaneous (SC) secukinumab was compared with SC treatments etanercept and its biosimilar, certolizumab pegol, adalimumab and its biosimilar, golimumab, ustekinumab, intravenous (IV) treatment infliximab, as well as oral non-biologic apremilast. Patients without prior exposure (naïve) to biologics and without moderate to severe psoriasis were considered for secukinumab 150 mg group. Secukinumab 300 mg group included naïve patients with moderate to severe psoriasis and all patients with prior biologic exposure. The PsA Response Criteria (PsARC) at 12-week was primary criteria for treatment response. Other clinical as well as cost related model inputs were derived from relevant clinical trials as well as Finnish publications. The key model outcomes were quality-adjusted life years and incremental cost-effectiveness ratio. An annual 3% discount rate was applied to all future costs and benefits. Model input variations were assessed through sensitivity analyses and alternative scenario analyses.ResultsFor a lifetime horizon (60 years), secukinumab 150 mg dominated all branded SC biologics and apremilast with highest QALY of 8.01 and lowest lifetime cost of €187,776, while it was cost-effective against IV infliximab among biologic-naïve patients without moderate to severe psoriasis. Secukinumab 300 mg was cost-effective against all branded SC biologics and apremilast and dominated IV infliximab among biologic-naïve patients with moderate to severe psoriasis, while it was cost-effective in biologic experienced patients. With the one-way sensitivity analysis, PsARC response, drug acquisition cost, and health assessment questionnaire score were the most important parameters affecting the outcomes. Across all treatment groups, patients on secukinumab were most likely to achieve highest net monetary benefit than other competitors in probabilistic sensitivity analysis. With alternative scenario analysis, results largely remained unchanged.ConclusionsSecukinumab is a cost-effective treatment for PsA patients from a Finnish payer’s perspective.

Highlights

  • Psoriatic arthritis (PsA), a disease associated with psoriasis, is a chronic, multiform inflammation of joints, entheses and tendons but can affect spine [1,2,3,4]

  • This study reports the results of a cost-effectiveness analysis of subcutaneous (SC) secukinumab versus currently licensed biologics, biosimilars (SC certolizumab pegol, etanercept and its biosimilar, adalimumab and its biosimilar, golimumab, ustekinumab and intravenous [IV] infliximab) and oral non biologic apremilast in Finland

  • The IV administered infliximab had slightly higher quality-adjusted life years (QALYs) (+ 0.06), but at an incremental cost-effectiveness ratio (ICER) of €680,427/QALY gained vs secukinumab

Read more

Summary

Introduction

Psoriatic arthritis (PsA), a disease associated with psoriasis, is a chronic, multiform inflammation of joints, entheses and tendons but can affect spine [1,2,3,4]. There are a lot of variations in the disease severity. Inflammation in PsA can lead to irreversible structural changes in joints and bones [5]. Incidence rates ranging from 10 to 23.1 per 100,000 person-years have been reported in local epidemiological studies [6, 7]. Painful joints and entheses limit patients’ daily activities, which along with psoriatic skin involvement, causes substantial lowering of health-related quality of life [8]. PsA is associated with comorbidities, especially cardiovascular diseases, and poses significant economic burden over healthcare systems [9]

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.