Department of Dermatology, Far Eastern Memorial Hospital , New Taipei, Taiwan.
Department of Dermatology, National Taiwan University Hospital and National Taiwan University College of Medicine , Taipei, Taiwan.
Expert Rev Clin Pharmacol. 2020 May;13(5):493-503. doi: 10.1080/17512433.2020.1767590. Epub 2020 May 27.
Advances of biologic agents have changed the treatment paradigm of psoriasis to higher efficacy and better quality of life. However, the demand for biologic switch is increasing due to patient's greater expectation and decreasing efficacy in long-term use. Also, biologic-induced adverse effects necessitate the switching of biologics.
This review article was divided into two parts. The first part focused on the biologic switch due to lack of efficacy. The second part provided switching suggestions related to adverse effects.
Biologic switch in psoriasis was mainly due to lack of efficacy, and the subsequent biologic agent was usually given at the next scheduled time point without washout period. In pivotal randomized controlled trials, patients with poor response to TNF-alpha inhibitors and ustekinumab achieved better efficacy after switching to IL-23 and IL-17 inhibitors. In addition, real-world data showed that intra-class switch could still achieve a 50%-80% of PASI 75 response in individuals with anti-IL-17 failure histories. As for the biologic switch due to adverse effects, washout period was recommended and transition to a biologic agent with different modes of action was preferred, especially class-specific adverse events.
生物制剂的进步改变了银屑病的治疗模式,提高了疗效和生活质量。然而,由于患者的期望更高,长期使用效果降低,对生物制剂的需求不断增加,需要进行生物制剂的转换。此外,生物制剂诱导的不良反应也需要进行药物转换。
本文综述分为两部分。第一部分重点介绍了因疗效不佳而进行的生物制剂转换。第二部分提供了与不良反应相关的转换建议。
银屑病的生物制剂转换主要是由于疗效不佳,随后的生物制剂通常在下一个预定的时间点给予,而无需冲洗期。在关键性随机对照试验中,对 TNF-α抑制剂和乌司奴单抗反应不佳的患者在转换为 IL-23 和 IL-17 抑制剂后疗效更好。此外,真实世界的数据表明,在抗 IL-17 治疗失败的患者中,同种药物转换仍可达到 PASI75 缓解率 50%-80%。对于因不良反应而进行的生物制剂转换,建议进行冲洗期,并优先选择作用机制不同的生物制剂,特别是针对特定类别的不良反应。