Practical experience of ustekinumab in the treatment of psoriasis: Experience from a multicentre, retrospective case cohort study across the U.K. and Ireland

Background There are limited data on the use of ustekinumab outside of clinical trials. Objectives To assess the efficacy and safety of ustekinumab in patients with severe psoriasis attending 10 dermatology centres in the U.K. and Ireland. Methods A retrospective case-note review of 129 patients with psoriasis treated with ustekinumab. Results Baseline Psoriasis Area and Severity Index (PASI) was 22Æ9 ± 10Æ1 (mean ± SD). After 16 weeks of treatment with ustekinumab PASI 75 (75% reduction in PASI) was observed in 63Æ0% (n = 80⁄127) of patients, although four patients required concomitant therapy at the 16-week time point. Previous biologic use did show a small, non-significant trend towards treatment failure. A PASI 75 response was seen in 29Æ4% (n = 5⁄17) of individuals weighing 90– 100 kg and treated with the standard 45 mg ustekinumab dose compared with PASI 75 of 70Æ3%, 71Æ4%, 75Æ0% and 55Æ6% for weight groups < 80, 80–90, 100–110 and > 110 kg, respectively (P = 0Æ024). Ustekinumab therapy was well tolerated; serious adverse events were observed in 2Æ3% (n = 3⁄129) of patients. Conclusions Ustekinumab is a novel biologic agent for psoriasis. When used in everyday clinical practice it demonstrates high levels of short-term therapeutic efficacy with an acceptable short-term safety profile