Luger T A, Lahfa M, Fölster-Holst R, Gulliver W P, Allen R, Molloy S, Barbier N, Paul C, Bos J D
Universitätsklinikum Münster, Hautklinik, Muenster Germany.
J Dermatolog Treat. 2004 Jun;15(3):169-78. doi: 10.1080/09546630410033781.
This randomized, double-blind, multi-centre study compared the long-term safety and tolerability of pimecrolimus cream 1% and topical corticosteroids (TCS) in 658 adults with moderate-severe atopic dermatitis (AD).
Patients applied either pimecrolimus or TCS (i.e. 0.1% triamcinolone acetonide cream and/or 1% hydrocortisone acetate cream) twice daily to all affected areas until complete clearance or for up to 1 year. The study was approved by the institutional review board or ethics committee at each centre.
A majority of patients treated with either pimecrolimus or TCS used the drug on a continuous basis over 1 year. In patients who had >30% of the body surface involved by AD, the incidence rate of all skin infections was significantly lower in the pimecrolimus group than in the TCS group (95% CI of the treatment difference: -25.3% to -3.4%). The most frequent application site reaction was burning (25.9% of patients on pimecrolimus and 10.9% on TCS), which was transient and mild-moderate in most cases. Three TCS-treated patients reported skin striae. There were no treatment-related serious or clinically significant systemic adverse events. Efficacy was better in patients on continuous TCS therapy, although patients completing the study were similarly well-controlled in both groups. About 42% of the pimecrolimus-treated patients were maintained for 1 year without TCS.
Pimecrolimus demonstrated a favourable safety profile when used to treat adult patients with moderate-severe AD for up to 1 year. A significant proportion of patients could be maintained without TCS for a year.
这项随机、双盲、多中心研究比较了1%吡美莫司乳膏与外用皮质类固醇(TCS)对658例中重度特应性皮炎(AD)成人患者的长期安全性和耐受性。
患者将吡美莫司或TCS(即0.1%曲安奈德乳膏和/或1%醋酸氢化可的松乳膏)每日两次涂抹于所有受累部位,直至完全清除或最长使用1年。该研究获得了各中心机构审查委员会或伦理委员会的批准。
大多数接受吡美莫司或TCS治疗的患者在1年多的时间里持续使用该药物。在AD累及体表面积>30%的患者中,吡美莫司组的所有皮肤感染发生率显著低于TCS组(治疗差异的95%CI:-25.3%至-3.4%)。最常见的用药部位反应是烧灼感(吡美莫司组25.9%的患者,TCS组10.9%的患者),在大多数情况下是短暂的,且为轻至中度。3例接受TCS治疗的患者报告有皮肤萎缩纹。没有与治疗相关的严重或具有临床意义的全身性不良事件。持续接受TCS治疗的患者疗效更好,尽管完成研究的患者在两组中控制情况相似。约42%接受吡美莫司治疗的患者在无TCS的情况下维持了1年。
吡美莫司用于治疗中重度AD成人患者长达1年时,显示出良好的安全性。相当一部分患者可以在无TCS的情况下维持1年。