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[Dermatology]
Elena Vladimirovna Svechnikova; Svetlana Evgenievna Zhufina; Natalia Alexandrovna Merzlikina; Vasily Stanislavovich Babanin; Elena Vasilevna Rzhevskaya;
Psoriasis and psoriatic arthritis require a long-term therapeutic control, and the study of biologic therapy survival helps optimize treatment and improve patients’ quality of life. A single-center cohort study conducted between 2017 and 2025 included 51 patients (59 % men, mean age 53.3±12.6 years, mean disease duration 14 [10; 24] years). The most frequently used drug was netakimab (52 %), followed by secukinumab (22 %), ixekizumab (16 %), and guselkumab (8 %); the mean follow up period was 3.3±1.72 years. Treatment survival was not influenced by sex, bio-naïve status, or presence of psoriatic arthritis (PsA), but was higher in patients over 39 years of age (p=0.028). Netakimab demonstrated the longest treatment duration, while guselkumab showed a shorter one (p=0.017), though with the lowest rate of adverse events (0 %); ixekizumab had the highest rate (20 %). These findings highlight the importance of an individualized approach to therapy selection and patient monitoring, which may improve clinical outcomes and treatment adherence. The results may be useful for both clinical practice and further research in biologic therapy, ultimately contributing to better quality of life in patients with psoriasis and PsA.
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Keywords: psoriasis, psoriatic arthritis, genetically engineered biological therapy, survival rate of biologics therapy