Switching from Secukinumab to Ustekinumab in Psoriasis Patients: Results from a Multicenter Experience.


Journal

Dermatology (Basel, Switzerland)
ISSN: 1421-9832
Titre abrégé: Dermatology
Pays: Switzerland
ID NLM: 9203244

Informations de publication

Date de publication:
2019
Historique:
received: 24 09 2018
accepted: 25 01 2019
pubmed: 1 4 2019
medline: 18 12 2019
entrez: 1 4 2019
Statut: ppublish

Résumé

Switching between biologics is commonly performed for the management of plaque psoriasis. However, no evidence about switching from secukinumab to ustekinumab has been reported. This retrospective observational multicenter study aimed to describe efficacy and safety of ustekinumab in secukinumab nonresponder patients. A total of 21 patients unresponsive to secukinumab were treated with ustekinumab for a mean period of 53.3 weeks. Ustekinumab was effective in reducing disease severity, with significant improvements of both psoriasis area severity index (PASI) and dermatology quality of life index (DLQI) scores. PASI score improvements of 31.8, 44, 77.8, 80.3, 80.5, and 89.6%, at week 4, 12, 24, 36, 48, and above 60 weeks, respectively, were detected (p < 0.05), achieving PASI 50, 75, and > 90 responses in 93.8, 87.5, and 50% of patients at week 48. Four patients withdrew from ustekinumab treatment because of inefficacy, and failure of multiple biologic agents (> 2) seemed to affect ustekinumab drug survival. No serious adverse events (AEs) were reported while 38.1% of patients experienced mild AEs. Ustekinumab was safe and effective in treating patients unresponsive to secukinumab.

Sections du résumé

BACKGROUND BACKGROUND
Switching between biologics is commonly performed for the management of plaque psoriasis. However, no evidence about switching from secukinumab to ustekinumab has been reported.
METHODS METHODS
This retrospective observational multicenter study aimed to describe efficacy and safety of ustekinumab in secukinumab nonresponder patients.
RESULTS RESULTS
A total of 21 patients unresponsive to secukinumab were treated with ustekinumab for a mean period of 53.3 weeks. Ustekinumab was effective in reducing disease severity, with significant improvements of both psoriasis area severity index (PASI) and dermatology quality of life index (DLQI) scores. PASI score improvements of 31.8, 44, 77.8, 80.3, 80.5, and 89.6%, at week 4, 12, 24, 36, 48, and above 60 weeks, respectively, were detected (p < 0.05), achieving PASI 50, 75, and > 90 responses in 93.8, 87.5, and 50% of patients at week 48. Four patients withdrew from ustekinumab treatment because of inefficacy, and failure of multiple biologic agents (> 2) seemed to affect ustekinumab drug survival. No serious adverse events (AEs) were reported while 38.1% of patients experienced mild AEs.
CONCLUSION CONCLUSIONS
Ustekinumab was safe and effective in treating patients unresponsive to secukinumab.

Identifiants

pubmed: 30928971
pii: 000497274
doi: 10.1159/000497274
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Biological Products 0
secukinumab DLG4EML025
Ustekinumab FU77B4U5Z0

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

213-218

Informations de copyright

© 2019 S. Karger AG, Basel.

Auteurs

Andrea Chiricozzi (A)

Institute of Dermatology, Catholic University - Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy, chiricozziandrea@gmail.com.
Dermatology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy, chiricozziandrea@gmail.com.

Andrea Conti (A)

Department of Head and Neck Surgery, Section of Dermatology, Azienda Ospedaliero Universitaria Policlinico di Modena, Modena, Italy.

Martina Burlando (M)

Section of Dermatology, University of Genoa, Di.S.Sal., San Martino Policlinic Hospital, Genoa, Italy.

Giulia Odorici (G)

Department of Head and Neck Surgery, Section of Dermatology, Azienda Ospedaliero Universitaria Policlinico di Modena, Modena, Italy.

Francesca Gaiani (F)

Dermatology Unit, Azienda Ospedaliera San Donato Milanese, Milan, Italy.

Salvatore Panduri (S)

Dermatology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Piergiorgio Malagoli (P)

Dermatology Unit, Azienda Ospedaliera San Donato Milanese, Milan, Italy.

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Classifications MeSH