Literature DB >> 31769703

Real-world treatment patterns and healthcare costs of biologics and apremilast among patients with moderate-to-severe plaque psoriasis by metabolic condition status.

Steven R Feldman1, Jingchuan Zhang2, Diane J Martinez3, Lorena Lopez-Gonzalez3, Elizabeth Hoit Marchlewicz3, George Shrady3, Alan M Mendelsohn2, Yang Zhao2.   

Abstract

OBJECTIVES: To compare treatment patterns and costs among psoriasis patients with and without metabolic conditions newly initiating a biologic or apremilast.
METHODS: Adult patients included had ≥1 prescription for secukinumab, adalimumab, ustekinumab, etanercept, or apremilast between 01/01/2015 and 08/31/2018 (date of first prescription was index date) and no index drug use in the 12-months pre-index, and continuous enrollment in the 12-month pre-index and 24-month post-index periods. Patients were divided into mutually exclusive treatment cohorts and stratified by their pre-index metabolic condition status. Treatment patterns (adherence, non-persistence, switching, discontinuation, use of combination therapy, and re-initiation) and healthcare costs were compared.
RESULTS: Overall, 7773 patients were included; 47.5-56.7% had a metabolic condition. Except for the apremilast group, patients with metabolic conditions had higher discontinuation (secukinumab: 50.6% vs. 43.7%; adalimumab*: 53.9% vs. 48.7%; ustekinumab*: 41.9% vs. 35.1%; etanercept: 42.8% vs. 41.2%; apremilast: 43.1% vs. 46.1%) and switching (secukinumab: 48.1% vs. 41.2%; adalimumab*: 47.8% vs. 41.9%; ustekinumab*: 34.5% vs. 25.3%; etanercept*: 53.6% vs. 51.5%; apremilast: 45.8% vs. 44.6%) than patients without (*p < .05). Patients with metabolic conditions incurred significantly higher costs.
CONCLUSION: Many psoriasis patients initiating biologics or apremilast had metabolic conditions. These patients had higher discontinuation and switching, and significantly higher healthcare costs.

Entities:  

Keywords:  Psoriasis; apremilast; biologic therapy; metabolic conditions

Mesh:

Substances:

Year:  2019        PMID: 31769703     DOI: 10.1080/09546634.2019.1698699

Source DB:  PubMed          Journal:  J Dermatolog Treat        ISSN: 0954-6634            Impact factor:   3.359


  5 in total

1.  Interleukin-17 Inhibitor Combination Therapies for the Treatment of Psoriasis: A Systematic Review.

Authors:  Amylee Martin; Akshitha Thatiparthi; Jeffrey Liu; Jashin J Wu
Journal:  J Clin Aesthet Dermatol       Date:  2022-06

2.  Effectiveness and clinical predictors of drug survival in psoriasis patients receiving apremilast: A registry analysis.

Authors:  Thomas Graier; Wolfgang Weger; Paul-Gunther Sator; Wolfgang Salmhofer; Barbara Gruber; Constanze Jonak; Claudia Kölli; Martina Schütz-Bergmayr; Igor Vujic; Gudrun Ratzinger; Nina Häring; Clemens Painsi; Knut Prillinger; Alexander Mlynek; Hans Skvara; Hannes Trattner; Adrian Tanew; Roland Lichem; Christina Ellersdorfer; Franz Legat; Alexandra Gruber-Wackernagel; Angelika Hofer; Erich Schmiedberger; Wolfram Hoetzenecker; Robert Müllegger; Werner Saxinger; Franz Quehenberger; Peter Wolf
Journal:  JAAD Int       Date:  2020-12-26

3.  Risk of Treatment Discontinuation among Patients with Psoriasis Initiated on Ustekinumab and Other Biologics in the USA.

Authors:  Dominic Pilon; Timothy Fitzgerald; Maryia Zhdanava; Amanda Teeple; Laura Morrison; Aditi Shah; Patrick Lefebvre
Journal:  Dermatol Ther (Heidelb)       Date:  2022-03-19

Review 4.  Clinical Efficacy and Safety of Psoriasis Treatments in Patients with Concomitant Metabolic Syndrome: A Narrative Review.

Authors:  Joseph F Merola; Arthur Kavanaugh; Mark G Lebwohl; Robert Gniadecki; Jashin J Wu
Journal:  Dermatol Ther (Heidelb)       Date:  2022-08-25

Review 5.  Adherence and Persistence to Biological Drugs for Psoriasis: Systematic Review with Meta-Analysis.

Authors:  Eugenia Piragine; Davide Petri; Alma Martelli; Agata Janowska; Valentina Dini; Marco Romanelli; Vincenzo Calderone; Ersilia Lucenteforte
Journal:  J Clin Med       Date:  2022-03-09       Impact factor: 4.241

  5 in total

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