Hren M Grace, Miriyala Sreekar, Khattri Saakshi
Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Clin Exp Dermatol. 2024 Dec 23;50(1):137-140. doi: 10.1093/ced/llae305.
Interleukin (IL)-23 inhibitors are a class of injectable biologics, which include risankizumab, tildrakizumab and guselkumab, used for the treatment of moderate-to-severe psoriasis. This retrospective review sought to determine the value of IL-23 inhibitor intraclass switching among patients with psoriasis after they experienced loss of efficacy to any IL-23 inhibitor. We conducted a retrospective chart review, including 43 patients who underwent any of 6 potential iterations of IL-23 intraclass switching between November 2017 and November 2023. Most commonly, patients switched from guselkumab or tildrakizumab to risankizumab (84%). On average, patients failed 2.3 biologic treatments (SD 1.3) prior to switching. Postswitching, 81% of patients achieved an affected body surface area (BSA) < 1% after 248.8 days (SD 126.5). BSA immediately prior to intraclass switch was 13.1 (SD 8.9) [95% confidence interval (CI) 10.4-15.8] and at most recent follow-up was 2.9 (SD 5.2) (95% CI 2.3-5.5). This research adds to a growing body of literature demonstrating the potential of IL-23 intraclass switching in the treatment of moderate-to-severe plaque psoriasis.
白细胞介素(IL)-23抑制剂是一类注射用生物制剂,包括司库奇尤单抗、替拉珠单抗和古塞奇尤单抗,用于治疗中重度银屑病。这项回顾性研究旨在确定银屑病患者在对任何IL-23抑制剂治疗失去疗效后,进行IL-23抑制剂类内转换的价值。我们进行了一项回顾性病历审查,纳入了2017年11月至2023年11月期间进行过6种可能的IL-23类内转换中的任何一种的43例患者。最常见的情况是,患者从古塞奇尤单抗或替拉珠单抗转换为司库奇尤单抗(84%)。平均而言,患者在转换前接受了2.3种生物制剂治疗(标准差1.3)。转换后,81%的患者在248.8天(标准差126.5)后受累体表面积(BSA)<1%。类内转换前的BSA为13.1(标准差8.9)[95%置信区间(CI)10.4-15.8],在最近一次随访时为2.9(标准差5.2)(95%CI 2.3-5.5)。这项研究为越来越多的文献增添了内容,证明了IL-23类内转换在治疗中重度斑块状银屑病方面的潜力。