Efficacy, safety, and drug survival of IL-23, IL-17, and TNF-alpha inhibitors for psoriasis treatment: a retrospective study

塞库金单抗 伊克泽珠单抗 医学 银屑病 阿达木单抗 银屑病面积及严重程度指数 乌斯特基努马 内科学 药品 白细胞介素17 肿瘤坏死因子α 英夫利昔单抗 皮肤病科 药理学 免疫学 细胞因子 银屑病性关节炎
作者
Paolo Dapavo,Niccolò Siliquini,Luca Mastorino,Gianluca Avallone,Martina Merli,Andrea Agostini,Caterina Cariti,Riccardo Viola,Elena Stroppiana,A Verrone,Michela Ortoncelli,Pietro Quaglino,Simone Ribero
出处
期刊:Journal of Dermatological Treatment [Informa]
卷期号:33 (4): 2352-2357 被引量:29
标识
DOI:10.1080/09546634.2021.1961998
摘要

Real-life studies in psoriasis are lacking. Many monoclonal antibodies targeting tumor-necrosis factor (TNF)-alpha, interleukin 17, and 23 are approved drugs for psoriasis treatment.To compare the short and long-term efficacy, safety, and drug survival of anti TNF-alpha, anti-IL-17, and anti-IL-23 in a large case series.Psoriasis area severity index (PASI) and retention rates for adalimumab, secukinumab, guselkumab, ixekizumab, and brodalumab were analised.A total of 263 patients were randomly selected among the five drugs register of the patients attending the Psoriasis Unit at the Turin University Hospital. The mean PASI at baseline was 14.3. Ixekizumab showed a significantly higher efficacy profile compared to other drugs in terms of PASI90 and PASI100 at week 12, 24, and week 48 even when adjusted for other confounding factors. This superiority was not followed by an expected higher drug survival. On the contrary, secukinumab was the only drug that showed a higher drug survival among bio-naïve patients.

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