Boswell Nicole D, Ries Alexa, Gordon Kenneth B, Singla Shikha
Department of Dermatology, Medical College of Wisconsin, Milwaukee, WI, USA.
Department of Rheumatology, Medical College of Wisconsin, Milwaukee, WI, USA.
Dermatol Ther (Heidelb). 2025 Jul 18. doi: 10.1007/s13555-025-01482-3.
Psoriatic arthritis (PsA) is a complex, heterogeneous disease affecting multiple domains which necessitates a nuanced approach to treatment. While tumor necrosis factor (TNF) inhibitors have historically been the preferred first line therapy, increasing evidence highlights the efficacy of interleukin (IL) 17 and IL-23 inhibitors, particularly in cases of nonresponse to TNF inhibitors. These targeted biologics offer additional therapeutic options, especially for those with concomitant psoriasis (PsO) and axial disease. The proposed biologic sequence derived from clinical trial data and expert opinion incorporates PsA disease severity as well as concomitant PsO and axial disease in the setting of biologic nonresponse. This approach aims to guide clinicians in selecting the most effective therapy while conserving future treatment options. However, gaps remain in understanding the sequential use of IL-17 and IL-23 inhibitors, particularly in axial disease, emphasizing the need for further research and real-world clinical data.
银屑病关节炎(PsA)是一种复杂的异质性疾病,会影响多个领域,因此需要采取细致入微的治疗方法。虽然肿瘤坏死因子(TNF)抑制剂历来是首选的一线治疗药物,但越来越多的证据表明白细胞介素(IL)-17和IL-23抑制剂的疗效显著,尤其是在对TNF抑制剂无反应的病例中。这些靶向生物制剂提供了更多的治疗选择,特别是对于那些同时患有银屑病(PsO)和中轴型疾病的患者。从临床试验数据和专家意见得出的拟议生物制剂使用顺序,在生物制剂无反应的情况下纳入了PsA疾病严重程度以及伴随的PsO和中轴型疾病。这种方法旨在指导临床医生选择最有效的治疗方法,同时保留未来的治疗选择。然而,在理解IL-17和IL-23抑制剂的序贯使用方面,尤其是在中轴型疾病中,仍然存在差距,这凸显了进一步研究和真实世界临床数据的必要性。