Pharmacodynamic analysis of apremilast in Japanese patients with moderate to severe psoriasis: Results from a phase 2b randomized trial.


Journal

The Journal of dermatology
ISSN: 1346-8138
Titre abrégé: J Dermatol
Pays: England
ID NLM: 7600545

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 04 10 2019
accepted: 11 08 2020
pubmed: 11 9 2020
medline: 15 5 2021
entrez: 10 9 2020
Statut: ppublish

Résumé

We evaluated the pharmacodynamic effects of apremilast in 69 patients who were included in biomarker subanalyses of a phase 2b study that demonstrated the long-term safety and efficacy of apremilast in Japanese adults with moderate to severe psoriasis. The association between cytokine levels and Psoriasis Area and Severity Index (PASI) improvement was evaluated using linear regression and Spearman's rank correlation coefficient analysis. At baseline, median plasma levels of interleukin (IL)-17A, IL-17F and IL-22 were elevated versus reference values for healthy individuals, whereas tumor necrosis factor-α levels were close to normal. With apremilast 30 mg b.i.d., there were significant associations between percentage change in PASI score and percentage change in IL-17A, IL-17F and IL-22 levels at week 16. Findings demonstrate that the efficacy of apremilast in psoriasis is associated with inhibition of key cytokines involved in the pathology of psoriasis.

Identifiants

pubmed: 32909643
doi: 10.1111/1346-8138.15596
pmc: PMC7821327
doi:

Substances chimiques

Thalidomide 4Z8R6ORS6L
apremilast UP7QBP99PN

Types de publication

Clinical Trial, Phase II Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

80-84

Subventions

Organisme : Celgene

Informations de copyright

© 2020 The Authors. The Journal of Dermatology published by John Wiley & Sons Australia, Ltd on behalf of Japanese Dermatological Association.

Références

J Am Acad Dermatol. 2015 Jul;73(1):37-49
pubmed: 26089047
Biochem Pharmacol. 2012 Jun 15;83(12):1583-90
pubmed: 22257911
J Dermatol. 2017 Aug;44(8):873-884
pubmed: 28391657
J Drugs Dermatol. 2018 Aug 1;17(8):835-840
pubmed: 30124722
J Allergy Clin Immunol. 2018 Sep;142(3):1010-1013.e6
pubmed: 29936103
Br J Dermatol. 2015 Dec;173(6):1387-99
pubmed: 26357944
J Drugs Dermatol. 2013 Aug;12(8):888-97
pubmed: 23986162
Cell Signal. 2014 Sep;26(9):2016-29
pubmed: 24882690

Auteurs

Shinichi Imafuku (S)

Fukuoka University, Fukuoka, Japan.

Osamu Nemoto (O)

Kojinkai Sapporo Skin Clinic, Sapporo, Japan.

Yukari Okubo (Y)

Tokyo Medical University, Tokyo, Japan.

Mayumi Komine (M)

Jichi Medical University, Shimotsuke, Japan.

Peter Schafer (P)

Celgene Corporation, Summit, New Jersey, USA.

Rosemary Petric (R)

Celgene Corporation, Summit, New Jersey, USA.

Mamitaro Ohtsuki (M)

Jichi Medical University, Shimotsuke, Japan.

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Classifications MeSH