Volz T, Caroli U, Lüdtke H, Bräutigam M, Kohler-Späth H, Röcken M, Biedermann T
Department of Dermatology, Eberhard Karls University, Liebermeisterstrasse 25, 72076 Tübingen, Germany.
Br J Dermatol. 2008 Sep;159(4):936-41. doi: 10.1111/j.1365-2133.2008.08726.x. Epub 2008 Jul 21.
Erosive oral lichen planus (EOLP) is a T-cell mediated inflammatory disease leading to severe pain and impairment. As current therapies are of limited efficacy, application of calcineurin inhibitors is considered to be a potential option.
To investigate the efficacy of pimecrolimus cream 1% (Elidel) compared with vehicle cream in the treatment of EOLP.
Twenty patients were enrolled in a prospective, double-blind, randomized, vehicle-controlled trial and assigned to either pimecrolimus or vehicle group. Study medication was applied for 30 days followed by 30 days of observation without therapy. In case of unresponsiveness, treatment was continued for 30 days with open-label pimecrolimus. EOLP was monitored on days 0, 30 and 60. Safety was assessed by patient documentation, measurement of pimecrolimus levels and blood counts.
Within 30 days erosions cleared completely in seven of 10 patients treated with pimecrolimus and in two of 10 patients treated with vehicle. The clinical EOLP 'composite score' including mucosal erosions and pain sensation was significantly reduced in the pimecrolimus-treated group compared with vehicle (P = 0.025). In the three of 10 patients not responding to pimecrolimus, EOLP cleared after an additional 30 days of treatment with pimecrolimus. Following termination of the therapy, sustained remission of EOLP was detected in 83% of patients demonstrating long-lasting effects of pimecrolimus treatment. No severe adverse events were observed. In five patients pimecrolimus blood levels were detected, all of which stayed below 4 ng mL(-1).
Pimecrolimus cream 1% effectively treats EOLP with long-lasting therapeutic effects and is therefore a promising therapeutic option for EOLP.
糜烂性口腔扁平苔藓(EOLP)是一种由T细胞介导的炎症性疾病,会导致严重疼痛和功能障碍。由于目前的治疗方法疗效有限,应用钙调神经磷酸酶抑制剂被认为是一种潜在的选择。
研究1%吡美莫司乳膏(爱宁达)与赋形剂乳膏相比治疗EOLP的疗效。
20名患者参加了一项前瞻性、双盲、随机、赋形剂对照试验,被分为吡美莫司组或赋形剂组。研究药物应用30天,随后30天不进行治疗观察。如果无反应,则继续使用开放标签的吡美莫司治疗30天。在第0、30和60天监测EOLP。通过患者记录、吡美莫司水平测量和血细胞计数评估安全性。
在30天内,10名接受吡美莫司治疗的患者中有7名糜烂完全清除,10名接受赋形剂治疗的患者中有2名糜烂完全清除。与赋形剂相比,吡美莫司治疗组包括黏膜糜烂和疼痛感觉的临床EOLP“综合评分”显著降低(P = 0.025)。在10名对吡美莫司无反应的患者中,有3名在额外30天的吡美莫司治疗后EOLP清除。治疗结束后,83%的患者检测到EOLP持续缓解,表明吡美莫司治疗具有持久效果。未观察到严重不良事件。在5名患者中检测到吡美莫司血药浓度,均低于4 ng mL(-1)。
1%吡美莫司乳膏能有效治疗EOLP,且具有持久的治疗效果,因此是EOLP一种有前景的治疗选择。