Interleukin-17 vs. Interleukin-23 Inhibitors in Pustular and Erythrodermic Psoriasis: A Retrospective, Multicentre Cohort Study.

erythrodermic psoriasis interleukin-17 inhibitors interleukin-23 inhibitors pustular psoriasis

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
19 Feb 2023
Historique:
received: 23 12 2022
revised: 23 01 2023
accepted: 16 02 2023
entrez: 25 2 2023
pubmed: 26 2 2023
medline: 26 2 2023
Statut: epublish

Résumé

Pustular and erythrodermic psoriasis are rare and difficult-to-treat conditions. It has recently been shown that interleukin (IL)-17 inhibitors can be very effective among patients with these forms of psoriasis; however, the potential of IL-23 inhibitors is largely unknown. The aim of this multicentre, retrospective study was to compare the safety, effectiveness, and drug survival of IL-17 and IL-23 inhibitors among patients affected by these rare forms of psoriasis. The study involved 27 patients with erythrodermic psoriasis and 59 with pustular psoriasis (36 with generalised pustular psoriasis and 23 with palmoplantar pustular psoriasis) treated with an IL-17 or IL-23 inhibitor. The effectiveness of the two drug classes was assessed using the disease-specific Psoriasis Area Severity Index (PASI) and the Investigator Global Assessment, which were evaluated at different time points. There was a consistent trend towards a higher rate of PASI 100 responses in the patients treated with IL-17 inhibitors compared with those treated with IL-23 inhibitors, and the other efficacy outcomes showed a similar trend. There was no significant between-drug class difference in efficacy at any of the time points in the erythrodermic psoriasis cohort, whereas PASI 90 and PASI 100 response rates were significantly higher among the pustular psoriasis patients receiving IL-17 inhibitors at week 12 (IL-23 19% vs. IL-17 54% and IL-23 6% vs. IL-17 40%, respectively) and the percentage of responders to IL-17 inhibition was significantly higher at week 24 (IL-23 25% vs. IL-17 74%). In conclusion, it is therefore reasonable to assume that IL-17 and IL-23 inhibitors are both effective when treating pustular and erythrodermic psoriasis.

Identifiants

pubmed: 36836196
pii: jcm12041662
doi: 10.3390/jcm12041662
pmc: PMC9962195
pii:
doi:

Types de publication

Journal Article

Langues

eng

Références

J Eur Acad Dermatol Venereol. 2022 Oct;36(10):e849-e851
pubmed: 35689497
J Drugs Dermatol. 2014 Mar;13(3):342-54
pubmed: 24595581
J Am Acad Dermatol. 2023 Jan;88(1):243-246
pubmed: 35588923
Case Rep Dermatol. 2022 May 30;14(2):138-143
pubmed: 35813835
J Dermatol Sci. 2017 Jan;85(1):20-26
pubmed: 27743912
J Am Acad Dermatol. 2022 Sep;87(3):705-709
pubmed: 35640798
J Eur Acad Dermatol Venereol. 2017 Nov;31(11):1792-1799
pubmed: 28585342
N Engl J Med. 2021 Dec 23;385(26):2431-2440
pubmed: 34936739
J Clin Pharmacol. 2019 Dec;59(12):1656-1668
pubmed: 31257614
J Eur Acad Dermatol Venereol. 2022 Jul;36(7):e502-e505
pubmed: 35224780
J Dermatol. 2018 May;45(5):529-539
pubmed: 29569397
Dermatol Ther. 2022 Sep;35(9):e15697
pubmed: 35796147
J Eur Acad Dermatol Venereol. 2022 Jul;36(7):e574-e576
pubmed: 35279885
Exp Dermatol. 2020 Nov;29(11):1088-1096
pubmed: 32780422
J Dtsch Dermatol Ges. 2022 Oct;20(10):1362-1364
pubmed: 36067528
J Dermatol. 2017 Apr;44(4):355-362
pubmed: 27726163

Auteurs

Gianluca Avallone (G)

Dermatology Clinic, Department of Medical Sciences, University of Turin, 10124 Turin, Italy.
Dermatology Unit, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
Department of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy.

Carlo Alberto Maronese (CA)

Dermatology Unit, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
Department of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy.

Giulia Murgia (G)

Dermatology Unit, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
Department of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy.

Carlo Giovanni Carrera (CG)

Dermatology Unit, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.

Luca Mastorino (L)

Dermatology Clinic, Department of Medical Sciences, University of Turin, 10124 Turin, Italy.

Gabriele Roccuzzo (G)

Dermatology Clinic, Department of Medical Sciences, University of Turin, 10124 Turin, Italy.

Paolo Dapavo (P)

Dermatology Clinic, Department of Medical Sciences, University of Turin, 10124 Turin, Italy.

Silvia Alberti-Violetti (S)

Dermatology Unit, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
Department of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy.

Pietro Quaglino (P)

Dermatology Clinic, Department of Medical Sciences, University of Turin, 10124 Turin, Italy.

Simone Ribero (S)

Dermatology Clinic, Department of Medical Sciences, University of Turin, 10124 Turin, Italy.

Angelo Valerio Marzano (AV)

Dermatology Unit, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
Department of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy.

Classifications MeSH