Department of Dermatology, Columbia University Medical Center, New York, New York.
Columbia University College of Physicians and Surgeons, New York, New York.
Dermatol Ther. 2018 Nov;31(6):e12656. doi: 10.1111/dth.12656. Epub 2018 Sep 27.
Lichen planopilaris (LPP) is an inflammatory cicatricial alopecia for which many different therapies are attempted with varying success. The Janus kinase (JAK) inhibitor, tofacitinib, has been shown to be effective in treating the noncicatricial alopecia, alopecia areata. As in alopecia areata, upregulation of interferon and JAK signaling may play a role in LPP. We retrospectively reviewed the cases of 10 patients with recalcitrant LPP who were treated with oral tofacitinib. Patients received oral tofacitinib 5 mg twice or three times daily for 2-19 months as either monotherapy or adjunctive therapy to other ongoing treatments including intralesional triamcinolone, hydroxychloroquine, and tacrolimus ointment. Eight patients had clinical improvement in LPP with tofacitinib as either monotherapy (4/10) or adjunctive therapy (4/10). LPP Activity Index (LPPAI) before and after treatment was measured in seven patients and was significantly different (6.22 before treatment, 3.08 after treatment; p value = .0014). Reduction in LPPAI ranged from 30 to 94%. One patient complained of 10 pound (4.5 kg) weight gain after 12 months on tofacitinib. No other adverse effects were reported. Treatment with oral tofacitinib either as monotherapy or adjunctive therapy can lead to measurable improvement in recalcitrant LPP.
瘢痕性类扁平苔藓(LPP)是一种炎症性瘢痕性脱发,有许多不同的治疗方法,但成功率不一。Janus 激酶(JAK)抑制剂托法替尼已被证明可有效治疗非瘢痕性脱发,如斑秃。与斑秃一样,干扰素和 JAK 信号的上调可能在 LPP 中起作用。我们回顾性分析了 10 例难治性 LPP 患者的病例,这些患者接受了口服托法替尼治疗。患者接受口服托法替尼 5 mg,每日两次或三次,治疗 2-19 个月,单药治疗或联合其他正在进行的治疗,包括皮损内曲安奈德、羟氯喹和他克莫司软膏。8 例患者接受托法替尼单药治疗(4/10)或联合治疗(4/10)后 LPP 得到改善。7 例患者测量了治疗前后的 LPP 活动指数(LPPAI),差异有统计学意义(治疗前 6.22,治疗后 3.08;p 值 = 0.0014)。LPPAI 降低幅度为 30%至 94%。1 例患者在托法替尼治疗 12 个月后体重增加了 10 磅(4.5 公斤)。无其他不良反应报告。口服托法替尼单药或联合治疗可导致难治性 LPP 有可衡量的改善。