银屑病
银屑病性关节炎
医学
计算生物学
生物信息学
生物
皮肤病科
作者
Andrea Spini,Giorgia Pellegrini,Ylenia Ingrasciotta,Luca L’Abbate,Chiara Bellitto,Massimo Carollo,Olivia Leoni,Martina Zanforlini,Domenica Ancona,Paolo Stella,Anna Cavazzana,Angela Scapin,Sara Lopes,Valeria Belleudi,Stefano Ledda,Paolo Carta,Paola Rossi,Lucian Ejlli,Ester Sapigni,Aurora Puccini
标识
DOI:10.1080/14712598.2024.2357381
摘要
BACKGROUND: Switch patterns among different biologics and from originators to biosimilars (and vice versa) can be complex in patients with psoriasis (PsO) and psoriatic arthritis (PsA). OBJECTIVE: The aim of this study was to describe switching patterns of biological drugs in PsO/PsA patients and to explore predictors of multiple switches and switch-back. RESEARCH DESIGN AND METHODS: A large-scale retrospective cohort study was conducted using the Italian VALORE database. Bio-naïve users treated for PsO/PsA during 2010-2022 were included. Time to switch/swap and predictors of multiple switches and switch-back were analyzed. RESULTS: < 0.001) for TNF-α inhibitors (2,068 days) than anti-IL (2,780 days). At 1 year of follow-up patients starting with IL-23 switched/swapped biological therapy less frequently than those with anti-IL-12/23 and anti-IL-17 (4.9% vs. 8.7% and 9.4%, respectively). Patients starting with anti-IL-12/23 reported a significantly lower risk of multiple switches and switch-back (0.74, 95% CI, 0.67-0.83; 0.58, 95% CI, 0.44-0.77, respectively) than those with TNF-α inhibitors. CONCLUSIONS: Patients with PsO/PsA starting with TNF-α inhibitors switch/swap more rapidly and frequently than those with anti-IL, which are also associated with a reduced risk of multiple switches during follow-up.
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