Albany Medical College, Albany, NY, USA.
Loma Linda School of Medicine, Loma Linda, CA, USA.
J Dermatolog Treat. 2022 Mar;33(2):626-636. doi: 10.1080/09546634.2020.1775775. Epub 2020 Jun 8.
Biologic medications are recent advances that have clinical significance in the treatment of moderate-to-severe AD. A systemic literature review was performed to examine the efficacy and safety of biologic therapies currently in phase II and phase III of clinical trials for moderate-to-severe AD. Our team searched the databases, PubMed, Google Scholar, and ClinicalTrials.gov, on September 2019 for studies pertaining to the use of biologic drugs in AD. Key words included each drug (lebrikizumab, tralokinumab, fezakinumab, etokimab, nemolizumab, tezepelumab, and GBR 830) or 'biologic drugs' or 'immunotherapies' combined with 'atopic dermatitis.' References within retrieved articles were also reviewed to identify potentially missed studies. A total of 19 articles were included in this review. Lebrikizumab, tralokinumab, fezakinumab, nemolizumab, and GBR 830 lead to statistically significant improvements in disease severity and multiple endpoint outcome scores. Tezepelumab and etokimab, however, did not demonstrate statistically significant changes in primary outcome endpoints. Further assessment of tezepelumab and etokimab are needed to assess their safety and efficacy in patients with moderate-to-severe AD. Tralokinumab, lebrikizumab, fezakinumab, nemolizumab, and GBR 830 are effective treatment options for adults with moderate-to-severe AD, but further large-scale studies are needed to confirm their efficacy as monotherapy in children with moderate-to-severe AD.
生物制剂是近年来在治疗中重度 AD 方面具有临床意义的进展。我们进行了系统的文献回顾,以检查目前处于 II 期和 III 期临床试验阶段的用于治疗中重度 AD 的生物疗法的疗效和安全性。我们的团队于 2019 年 9 月在数据库、PubMed、Google Scholar 和 ClinicalTrials.gov 上搜索了与 AD 中生物药物使用相关的研究。关键词包括每种药物(利布昔单抗、特洛金单抗、法扎津单抗、依妥单抗、那莫利珠单抗、替泽单抗和 GBR 830)或“生物药物”或“免疫疗法”与“特应性皮炎”相结合。还审查了检索文章中的参考文献,以确定可能遗漏的研究。共有 19 篇文章纳入本综述。利布昔单抗、特洛金单抗、法扎津单抗、那莫利珠单抗和 GBR 830 可显著改善疾病严重程度和多个终点结局评分。然而,替泽单抗和依妥单抗在主要结局终点上没有显示出统计学上的显著变化。需要进一步评估替泽单抗和依妥单抗,以评估它们在中重度 AD 患者中的安全性和疗效。特洛金单抗、利布昔单抗、法扎津单抗、那莫利珠单抗和 GBR 830 是中重度 AD 成人的有效治疗选择,但需要进一步的大规模研究来确认它们作为中重度 AD 儿童单药治疗的疗效。