Cost-effectiveness of tildrakizumab for the treatment of moderate-to-severe psoriasis in the United States.
Cost-effectiveness
United States
plaque psoriasis
tildrakizumab
Journal
The Journal of dermatological treatment
ISSN: 1471-1753
Titre abrégé: J Dermatolog Treat
Pays: England
ID NLM: 8918133
Informations de publication
Date de publication:
Mar 2022
Mar 2022
Historique:
pubmed:
1
7
2020
medline:
8
4
2022
entrez:
1
7
2020
Statut:
ppublish
Résumé
To evaluate the relative cost-effectiveness of tildrakizumab and other biologic and targeted systemic treatments compared with a mix of topical therapies, phototherapies, and other conventional systemic therapies as first-line treatment for moderate-to-severe plaque psoriasis from a United States payer's perspective. A Markov model consisting of health states based on Psoriasis Area Severity Index (PASI) response rate categories and death was developed. The probabilities of achieving PASI responses were derived from a network meta-analysis based on published efficacy data. Health care costs and effectiveness measured in quality-adjusted life-years (QALYs) were estimated. Incremental costs per QALY gained of each biologic/targeted first-line treatment versus a mix of conventional treatments were compared to provide relative cost-effectiveness among biologic and targeted first-line treatments. Over 10 years, the incremental cost per QALY gained compared with a mix of topical therapies, phototherapies, and other oral systemic therapies was lowest for brodalumab, infliximab, apremilast, and tildrakizumab, followed by secukinumab, ixekizumab, guselkumab, adalimumab, ustekinumab, and etanercept. The position of tildrakizumab relative to the other treatments remained the same across multiple scenarios. Tildrakizumab is among the most cost-effective first-line therapies for moderate-to-severe plaque psoriasis and is more cost-effective than secukinumab, ixekizumab, guselkumab, adalimumab, ustekinumab, and etanercept.
Identifiants
pubmed: 32602762
doi: 10.1080/09546634.2020.1773382
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
tildrakizumab
DEW6X41BEK
Ustekinumab
FU77B4U5Z0
Types de publication
Journal Article
Meta-Analysis
Langues
eng
Sous-ensembles de citation
IM