Staab Doris, Pariser David, Gottlieb Alice B, Kaufmann Roland, Eichenfield Laurence F, Langley Richard G, Scott Graham, Ebelin Marie-Eve, Barilla Denise, Schmidli Heinz, Burtin Pascale
Department for Pediatric Pneumology and Immunology, Charité Campus Virchow, Berlin, Germany.
Pediatr Dermatol. 2005 Sep-Oct;22(5):465-71. doi: 10.1111/j.1525-1470.2005.00128.x.
Pimecrolimus cream 1%, a nonsteroid inhibitor of inflammatory cytokines, offers an alternative to corticosteroids in the treatment of atopic dermatitis. Here we evaluate pimecrolimus blood concentrations and tolerability to pimecrolimus cream 1% in 22 infants below 2 years of age with atopic dermatitis (10-92% body surface area affected at baseline). Efficacy was assessed as a secondary objective. Pimecrolimus cream 1% was applied twice daily for 3 weeks. Blood concentrations were low, typically (96% of total 100 concentrations measured) below 2 ng/mL, the majority (71%) remaining below 0.5 ng/mL. The highest concentration observed was 2.26 ng/mL. At steady state, there was no indication of accumulation. Pimecrolimus was well tolerated locally and systemically, with no serious adverse events recorded. Most adverse events recorded (35 in 17/22 patients) were typical of the young pediatric population studied, of mild to moderate severity, and not considered to be study-medication related, with the exception of four local adverse effects limited to the site of cream application. No clinically relevant change was observed in physical examination, vital signs, or laboratory safety parameters. A rapid onset of therapeutic effect was observed within the first four days of treatment. Pimecrolimus cream 1% is well tolerated in infants 3 to 23 months of age treated for 3 weeks, and results in minimal systemic exposure.
1%吡美莫司乳膏是一种炎性细胞因子的非甾体抑制剂,在特应性皮炎的治疗中可作为皮质类固醇的替代药物。在此,我们评估了22例2岁以下患有特应性皮炎(基线时体表面积受累10%-92%)的婴儿使用1%吡美莫司乳膏后的血药浓度及耐受性。疗效评估作为次要目标。1%吡美莫司乳膏每天涂抹两次,共3周。血药浓度较低,通常(所测的100个浓度中96%)低于2 ng/mL,大多数(71%)低于0.5 ng/mL。观察到的最高浓度为2.26 ng/mL。在稳态时,没有蓄积迹象。吡美莫司局部和全身耐受性良好,未记录到严重不良事件。记录的大多数不良事件(17/22例患者中的35例)是所研究的小儿群体的典型情况,为轻至中度严重程度,除了4例仅限于乳膏涂抹部位的局部不良反应外,均不认为与研究用药有关。体格检查、生命体征或实验室安全参数未观察到临床相关变化。在治疗的前四天内观察到治疗效果迅速显现。1%吡美莫司乳膏在3至23个月大的婴儿中治疗3周耐受性良好,全身暴露量最小。