a Center for Dermatology Research, Department of Dermatology , Wake Forest School of Medicine , Winston-Salem , NC , USA.
b Department of Pathology , Wake Forest School of Medicine , Winston-Salem , NC , USA.
Expert Opin Pharmacother. 2019 Jun;20(9):1057-1063. doi: 10.1080/14656566.2019.1604688. Epub 2019 Apr 19.
Atopic dermatitis (AD) is a chronic and recurrent disease presenting with eczematous lesions and pruritus. It impacts patient and family quality of life, increases morbidity, and accounts for large health-care expenditures. Although nonpharmacologic, topical, and systemic treatments exist, management of AD remains challenging due to limited treatment options. Crisaborole is a topical small molecule inhibitor of phosphodiesterase 4 (PDE4), recently approved for the treatment of AD in the United States. Areas covered: The authors review crisaborole in the management of AD based on Phase II, Phase III, and post-marketing studies. Pharmacologic properties such as chemistry, pharmacokinetics, pharmacodynamics and metabolism are discussed. A PubMed systematic review was augmented with Google Scholar searches via keyword, Medical Subject Headings (MeSH), and Boolean operation searches. Expert opinion: Crisaborole showed modest efficacy in short-term trials, but head-to-head trials with topical corticosteroids and tacrolimus are needed to assess its clinical utility. Since crisaborole is non-steroidal, it may reduce the need for topical corticosteroids and address steroid phobia. However, it is likely to suffer from the same factors contributing to intentional non-adherence in topicals: dissatisfaction with efficacy and inconvenience.
特应性皮炎(AD)是一种慢性复发性疾病,表现为湿疹样皮损和瘙痒。它影响患者及其家庭的生活质量,增加发病率,并导致大量医疗保健支出。尽管存在非药物、局部和全身治疗方法,但由于治疗选择有限,AD 的管理仍然具有挑战性。Crisaborole 是一种磷酸二酯酶 4(PDE4)的局部小分子抑制剂,最近在美国被批准用于 AD 的治疗。
作者根据 II 期、III 期和上市后研究,综述了 crisaborole 在 AD 管理中的应用。讨论了药理学特性,如化学、药代动力学、药效学和代谢。通过关键词、医学主题词(MeSH)和布尔操作搜索,对 PubMed 系统评价进行了补充,并在 Google Scholar 上进行了搜索。
crisaborole 在短期试验中显示出适度的疗效,但需要与局部皮质类固醇和他克莫司进行头对头试验,以评估其临床实用性。由于 crisaborole 是非甾体类药物,它可能减少对局部皮质类固醇的需求,并解决对皮质类固醇的恐惧。然而,它可能会受到导致局部用药非依从性的相同因素的影响:对疗效和不便的不满。