Efficacy, safety, and drug survival of IL-23, IL-17, and TNF-alpha inhibitors for psoriasis treatment: a retrospective study.


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:
Jun 2022
Historique:
pubmed: 29 7 2021
medline: 12 7 2022
entrez: 28 7 2021
Statut: ppublish

Résumé

Real-life studies in psoriasis are lacking. Many monoclonal antibodies targeting tumor-necrosis factor (TNF)-alpha, interleukin 17, and 23 are approved drugs for psoriasis treatment. To compare the short and long-term efficacy, safety, and drug survival of anti TNF-alpha, anti-IL-17, and anti-IL-23 in a large case series. Psoriasis area severity index (PASI) and retention rates for adalimumab, secukinumab, guselkumab, ixekizumab, and brodalumab were analised. A total of 263 patients were randomly selected among the five drugs register of the patients attending the Psoriasis Unit at the Turin University Hospital. The mean PASI at baseline was 14.3. Ixekizumab showed a significantly higher efficacy profile compared to other drugs in terms of PASI90 and PASI100 at week 12, 24, and week 48 even when adjusted for other confounding factors. This superiority was not followed by an expected higher drug survival. On the contrary, secukinumab was the only drug that showed a higher drug survival among bio-naïve patients.

Sections du résumé

BACKGROUND UNASSIGNED
Real-life studies in psoriasis are lacking. Many monoclonal antibodies targeting tumor-necrosis factor (TNF)-alpha, interleukin 17, and 23 are approved drugs for psoriasis treatment.
OBJECTIVES UNASSIGNED
To compare the short and long-term efficacy, safety, and drug survival of anti TNF-alpha, anti-IL-17, and anti-IL-23 in a large case series.
METHODS UNASSIGNED
Psoriasis area severity index (PASI) and retention rates for adalimumab, secukinumab, guselkumab, ixekizumab, and brodalumab were analised.
RESULTS UNASSIGNED
A total of 263 patients were randomly selected among the five drugs register of the patients attending the Psoriasis Unit at the Turin University Hospital. The mean PASI at baseline was 14.3. Ixekizumab showed a significantly higher efficacy profile compared to other drugs in terms of PASI90 and PASI100 at week 12, 24, and week 48 even when adjusted for other confounding factors. This superiority was not followed by an expected higher drug survival. On the contrary, secukinumab was the only drug that showed a higher drug survival among bio-naïve patients.

Identifiants

pubmed: 34315331
doi: 10.1080/09546634.2021.1961998
doi:

Substances chimiques

Immunologic Factors 0
Interleukin-17 0
Tumor Necrosis Factor Inhibitors 0
Tumor Necrosis Factor-alpha 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2352-2357

Auteurs

Paolo Dapavo (P)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Niccolò Siliquini (N)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Luca Mastorino (L)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Gianluca Avallone (G)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Martina Merli (M)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Andrea Agostini (A)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Caterina Cariti (C)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Riccardo Viola (R)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Elena Stroppiana (E)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Anna Verrone (A)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Michela Ortoncelli (M)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Pietro Quaglino (P)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

Simone Ribero (S)

Department of Medical Sciences, Section of Dermatology, University of Turin, Torino, Italy.

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