Faculty of Medicine, University of Western Ontario, London, Ontario, Canada.
Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
J Cutan Med Surg. 2023 May-Jun;27(3):271-276. doi: 10.1177/12034754231156100. Epub 2023 Feb 23.
Lichen Planus (LP) is a dermatological disorder characterized by violaceous papules that affect the cutaneous region, nails, scalp, and mucous membranes. Current molecular and clinical studies point to the Janus Kinase-signal transducer and activator of transcription (JAK-STAT) pathway as a potential effector of LP pathology.
This systematic review summarizes the current reported literature outcomes for patients receiving JAK inhibitors to treat LP.
MEDLINE and Embase were searched on 16 October, 2022, and 15 original articles were included, with 56 LP patients.
(mean age: 54.5 years, range: 26-81 years, male: 26.8%). The treatment outcomes were included for the following JAK inhibitors: tofacitinib ( = 30), baricitinib ( = 16), ruxolitinib ( = 12), and upadacitinib ( = 2). Patient outcomes were classified into complete resolution, partial resolution, and no resolution. Patients achieving complete resolution represented 25% ( = 4/16) in the baricitinib group, 10% ( = 3/30) in the tofacitinib group, 16.7% ( = 2/12) in the ruxolitinib group, and 100% (2/2) in the upadacitinib group. Partial resolution patients represented 31.3% ( = 5/16) of baricitinib patients, 60% ( = 18/30) of tofacitinib patients, and 83% ( = 10/12) of ruxolitinib patients. 43.8% ( = 7/16) of baricitinib patients and 10% ( = 9/30) of tofacitinib patients had no resolution of lesions.
This review also highlights the significance of utilizing a uniform outcome measure for LP, as it aids in reporting more generalizable results, reduces reporting bias, and ultimately lead to improved clinical outcomes for LP patients.
扁平苔藓(LP)是一种皮肤科疾病,表现为影响皮肤、指甲、头皮和黏膜的紫红色丘疹。目前的分子和临床研究表明,Janus 激酶-信号转导和转录激活因子(JAK-STAT)途径可能是 LP 发病机制的潜在效应物。
本系统综述总结了目前报道的接受 JAK 抑制剂治疗 LP 的患者的文献结果。
于 2022 年 10 月 16 日检索 MEDLINE 和 Embase,纳入 15 篇原始文章,共 56 例 LP 患者。
(平均年龄:54.5 岁,范围:26-81 岁,男性:26.8%)。纳入的 JAK 抑制剂治疗结果如下:托法替尼( = 30)、巴瑞替尼( = 16)、鲁索利替尼( = 12)和乌帕替尼( = 2)。患者结局分为完全缓解、部分缓解和无缓解。完全缓解的患者在巴瑞替尼组占 25%( = 4/16),在托法替尼组占 10%( = 3/30),在鲁索利替尼组占 16.7%( = 2/12),在乌帕替尼组占 100%(2/2)。部分缓解的患者在巴瑞替尼组占 31.3%( = 5/16),在托法替尼组占 60%( = 18/30),在鲁索利替尼组占 83%( = 10/12)。巴瑞替尼组 43.8%( = 7/16)和托法替尼组 10%( = 9/30)的患者皮损无缓解。
本综述还强调了为 LP 使用统一结局测量的重要性,因为这有助于报告更具普遍性的结果,减少报告偏倚,并最终改善 LP 患者的临床结局。