TY - JOUR
T1 - Real-world effectiveness of anti-interleukin-23 antibodies in chronic plaque-type psoriasis of patients from the Austrian Psoriasis Registry (PsoRA)
AU - Graier, T
AU - Weger, W
AU - Jonak, C
AU - Sator, P
AU - Zikeli, C
AU - Prillinger, K
AU - Sassmann, C
AU - Gruber, B
AU - Saxinger, W
AU - Ratzinger, G
AU - Painsi, C
AU - Mlynek, A
AU - Häring, N
AU - Sadoghi, B
AU - Trattner, H
AU - Müllegger, R
AU - Quehenberger, F
AU - Salmhofer, W
AU - Wolf, Peter
N1 - Funding Information:
PsoRA has been supported by unrestricted research grants or educational grants from the following pharmaceutical companies: AbbVie, Amgen GmbH, Almirall, Astropharma, Boehringer-Ingelheim , BMS, Celgene, Eli Lilly, Janssen-Cilag, Leo Pharma, Novartis, Merck Sharp & Dohme, Sandoz, UCB Pharma and Pfizer.
Funding Information:
We thank the patients participating in PsoRA and all members of PsoRA (see grtps://psora.medunigraz.at/) who provided data for this analysis. Special thanks go to Matthias Wagner, Vienna, for development of the original electronic PsoRA database; Erich Schmiedberger, administrator of the newly developed electronic database; Maximilian Errath for technical support; and Andrea Berghold, Department chair, Institute for Medical Informatics, Statistics, and Documentation for continuous support in further development of the PsoRA database. We also thank Franz Trautinger, University Hospital of St. Poelten, Karl Landsteiner University of Health Sciences, Krems, Austria, for continuous support in promoting further development of PsoRA. Martina Praszl-Posch and Kirsten Sommer for support of data entry in the PsoRa database, Sara Crockett, Graz, Austria for editing of the manuscript. This work has been conducted as part of a doctoral thesis (T.G.).
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - With the introduction of the latest class of biologic drugs targeting interleukin (IL)-23p19, three new, highly effective drugs can be used for the treatment of chronic plaque psoriasis. However, poorer skin improvement as well as higher rates of serious adverse events have been reported for patients under real-world conditions (outside clinical trials). This accounts especially for patients who have already been treated with biologic drugs. We therefore aimed to determine effectiveness and safety of IL-23p19 inhibitors in real-world patients by analysing data from the Psoriasis Registry Austria (PsoRA) in this observational, retrospective, multicentre cohort study. Data for 197 patients (52.3% biologic-non-naïve), who were treated with anti-IL-23p19 antibodies (127 guselkumab, 55 risankizumab and 15 tildrakizumab) for at least 3 months, were eligible for analysis. In general, biologic-non-naïve patients displayed a less favourable response to anti-IL-23 treatment as compared to biologic-naïve patients. However, after correction for previous biologic exposure, few differences in PASI improvement were detected among biologic-naïve and -non-naïve patients treated with different IL-23p19 inhibitors. This indicates that treatment effectiveness is not related to the class of the previously administered therapy in biologic-non-naïve patients. Therefore, IL-23p19 inhibitors represent a promising treatment alternative for patients who have not responded to previous biologics. However, as with other biologic agents (including IL-17 inhibitors), we did not observe an entirely satisfactory treatment response (i.e. PASI < 3 and/or PASI 75) to anti-IL-23 treatment in one out of four to five patients. Adverse events (mainly non-severe infections) were observed in 23 (11.7%) patients with no major differences regarding the administered IL-23 inhibitor or previous biologic exposure.
AB - With the introduction of the latest class of biologic drugs targeting interleukin (IL)-23p19, three new, highly effective drugs can be used for the treatment of chronic plaque psoriasis. However, poorer skin improvement as well as higher rates of serious adverse events have been reported for patients under real-world conditions (outside clinical trials). This accounts especially for patients who have already been treated with biologic drugs. We therefore aimed to determine effectiveness and safety of IL-23p19 inhibitors in real-world patients by analysing data from the Psoriasis Registry Austria (PsoRA) in this observational, retrospective, multicentre cohort study. Data for 197 patients (52.3% biologic-non-naïve), who were treated with anti-IL-23p19 antibodies (127 guselkumab, 55 risankizumab and 15 tildrakizumab) for at least 3 months, were eligible for analysis. In general, biologic-non-naïve patients displayed a less favourable response to anti-IL-23 treatment as compared to biologic-naïve patients. However, after correction for previous biologic exposure, few differences in PASI improvement were detected among biologic-naïve and -non-naïve patients treated with different IL-23p19 inhibitors. This indicates that treatment effectiveness is not related to the class of the previously administered therapy in biologic-non-naïve patients. Therefore, IL-23p19 inhibitors represent a promising treatment alternative for patients who have not responded to previous biologics. However, as with other biologic agents (including IL-17 inhibitors), we did not observe an entirely satisfactory treatment response (i.e. PASI < 3 and/or PASI 75) to anti-IL-23 treatment in one out of four to five patients. Adverse events (mainly non-severe infections) were observed in 23 (11.7%) patients with no major differences regarding the administered IL-23 inhibitor or previous biologic exposure.
KW - Austria/epidemiology
KW - Biological Products/therapeutic use
KW - Cohort Studies
KW - Graft vs Host Disease/drug therapy
KW - Humans
KW - Interleukin-23
KW - Psoriasis/drug therapy
KW - Registries
KW - Retrospective Studies
KW - Severity of Illness Index
KW - Treatment Outcome
UR - http://www.scopus.com/inward/record.url?scp=85137232917&partnerID=8YFLogxK
U2 - 10.1038/s41598-022-18790-9
DO - 10.1038/s41598-022-18790-9
M3 - Journal article
C2 - 36064563
SN - 2045-2322
VL - 12
SP - 15078
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 15078
ER -