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. 2025 May 13:24755303251342503.
doi: 10.1177/24755303251342503. Online ahead of print.

Ixekizumab Retention Rate and Predictors of Treatment Persistence in Psoriatic Arthritis: Results of an Italian Multicenter Study

Camilla Mazzanti  1 Marino Paroli  2 Gianluca Santoboni  1 Olga Addimanda  3 Bernd Raffeiner  4 Alessandra Bezzi  5 Elisa Visalli  6 Eleonora Celletti  7 Antonella Farina  8 Simone Bernardi  9 Maddalena Larosa  10 Romina Andracco  11 Patrizia Del Medico  12 Aldo Biagio Colella Molica  13 Dilia Giuggioli  14 Federica Lumetti  14 Gilda Sandri  14 Marta Priora  15 Francesca Serale  15 Valeria Nucera  16 Francesca Ometto  17 Elena Bravi  18 Alberto Lo Gullo  19 Palma Scolieri  20 Simone Parisi  21 Viviana Ravagnani  22 Rosetta Vitetta  23 Antonio Marchetta  24 Andrea Becciolini  25 Claudio Angrisani  1 Massimiliano De Simone  1 Rosalba Caccavalle  2 Massimo Reta  3 Mirco Magnani  3 Fabio Mascella  5 Roberta Foti  6 Giorgio Amato  6 Francesco De Lucia  6 Ylenia Dal Bosco  6 Rosario Foti  6 Myriam Di Penta  7 Emanuela Sabatini  7 Pietro Del Biondo  7 Francesco Girelli  9 Dario Camellino  10 Gerolamo Bianchi  10 Natalia Mansueto  11 Gianluca Smerilli  12 Veronica Franchina  13 Carlo Salvarani  14 Aurora Ianniello  16 Cecilia Giampietro  17 Eleonora Di Donato  26 Daniele Santilli  26 Gianluca Lucchini  26 Eugenio Arrigoni  18 Ilaria Platè  18 Vincenzo Bruzzese  20 Enrico Fusaro  21 Maria Chiara Ditto  21 Davide Murgia  23 Guido Rovera  23 Alessandro Volpe  24 Giulio Ferrero  26 Giuditta Adorni  25 Francesco Colella Molica  27 Alarico Ariani  25
Affiliations

Ixekizumab Retention Rate and Predictors of Treatment Persistence in Psoriatic Arthritis: Results of an Italian Multicenter Study

Camilla Mazzanti et al. J Psoriasis Psoriatic Arthritis. .

Abstract

IXE (Ixekizumab) is a monoclonal antibody targeting interleukin-17A (IL17A) which has demonstrated significant efficacy and safety in the management of psoriatic arthritis (PsA) in randomized controlled trials (RCTs). However, available data on long-term persistence of therapy are scarce.

Methods: This multi-center study aimed to evaluate the drug retention rate (DRR) of IXE in a real-world setting and to identify key factors influencing treatment persistence. 195 patients with PsA treated with IXE between 2018 and 2024 were included. The primary outcome was DRR, calculated at 360, 720, and 1080 days after treatment initiation. Clinical and demographic factors were analyzed as potential predictors of IXE treatment permanency.

Results: IXE retention rates were 66% at 360 days, 49% at 720 days, and 39% at 1080 days. Low baseline disease activity was a strong predictor of higher retention (HR 0.24, 95% CI: 0.09-0.62, p = 0.003), while younger age was significantly associated with improved persistence (HR 0.98, 95% CI: 0.96-1.00, p = 0.045). Conversely, patients with both axial and peripheral joint involvement were more likely to discontinue therapy (HR 1.78, 95% CI: 1.04-3.06, p = 0.036), as were those receiving IXE as a second- or third-line therapy (HR 1.17, 95% CI: 1.02-1.33, p = 0.021).

Conclusions: This multicenter real-world study confirms the long-term retention rate of IXE in PsA. The findings highlight key factors influencing treatment persistence and provide valuable insights to optimize patient management. Further real-world research is needed to better understand the therapeutic performance of IXE in different patient populations.

Keywords: biologic treatment; comparative effectiveness; interleukin 17 inhibitor; ixekizumab; psoriasis; psoriatic arthritis.

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Conflict of interest statement

The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: Ariani A has received honoraria as a speaker and an advisory board member for AbbVie, Abiogen, Amgen, Bristol-Myers Squibb, Boehringer, Bruno Farmaceutici, Stada EG, Janssen, Lilly, Novartis, Novo Nordisk, Sanofi, and Zentiva. Lumetti F has received honoraria as an advisory board member for Amgen. None of the other authors have any potential conflicts of interest to disclose in relation to this work.

Figures

Figure 1.
Figure 1.
Kaplan-Meier Curve for Ixekizumab Drug Survival. Drug retention rate for IXE expressed in days: 365 days = 12 months; 730 days = 24 months; 1095 days = 36 months. The X-axis represents the observation time, while the Y-axis shows the probability of remaining on therapy. The number of patients at risk is indicated below the graph.
Figure 2.
Figure 2.
Cox Regression Analysis of Hazard Ratios (HR). The regression model evaluates the HR of various factors associated with the continuation of therapy over time. An HR >1 indicates an increased risk of discontinuing therapy, while an HR <1 suggests a reduced risk. Confidence intervals (CI) and P-values are reported for each factor to indicate statistical significance.

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