Gollnick Harald, Barona Carlos Guillén, Frank Ronald G J, Ruzicka Thomas, Megahed Mosaad, Tebbs Veronica, Owens Mary, Stampone Patti
Universitätsklinik für Dermatologie und Venerologie, Otto-von-Guericke-Universität Magdeburg,Leipziger Str. 44, 39120 Magdeburg, Germany.
Eur J Dermatol. 2005 Sep-Oct;15(5):374-81.
Imiquimod is an immune response modifier that acts through Toll-like receptor 7 to induce innate and cell-mediated immune responses. This ongoing phase III, open-label study conducted in Europe is evaluating the long-term (5 year) clinical efficacy and safety of imiquimod 5% cream applied once daily 5 times per week (5 x/week) for 6 weeks for the treatment of superficial basal cell carcinoma (sBCC). A total of 182 subjects were enrolled. The initial sBCC clearance rate was 90% (12-week post treatment), whereas the proportion of subjects who were clinically clear at 2 years (current time point) was estimated to be 79.4%. Local skin/application site reactions were the most frequently reported safety findings. Initial efficacy rates of imiquimod applied 5 x/week for 6 weeks demonstrate its clinical utility as an alternative approach to the treatment of sBCC. The recurrence rate seen to date supports ongoing follow up of subjects treated with imiquimod.
咪喹莫特是一种免疫反应调节剂,它通过Toll样受体7发挥作用,诱导先天性和细胞介导的免疫反应。这项正在欧洲进行的III期开放标签研究,正在评估每周5次、每天1次外用5%咪喹莫特乳膏、持续6周治疗浅表性基底细胞癌(sBCC)的长期(5年)临床疗效和安全性。总共招募了182名受试者。初始sBCC清除率为90%(治疗后12周),而在2年(当前时间点)临床清除的受试者比例估计为79.4%。局部皮肤/用药部位反应是最常报告的安全性发现。每周5次、持续6周外用咪喹莫特的初始有效率证明了其作为sBCC治疗替代方法的临床效用。迄今为止观察到的复发率支持对接受咪喹莫特治疗的受试者进行持续随访。