Department of Dermatology, Monklands Hospital, Airdrie, Lanarkshire, UK.
Department of Dermatology, Charité - University Medical Centre Berlin, Berlin, Germany.
J Eur Acad Dermatol Venereol. 2015 Sep;29(9):1840-2. doi: 10.1111/jdv.12697. Epub 2014 Aug 29.
In patients with actinic keratosis (AK), subclinical and clinical lesions coexist across large areas of sun-exposed skin. The long-term efficacy of AK treatments depends on their ability to eradicate both types of lesions across the entire field.
To assess the long-term efficacy of imiquimod 3.75% using the reduction in lesions from Lmax (maximum lesion count during treatment), which assesses the ability to clear subclinical and clinical lesions.
Patients with 5-20 AK lesions on the full face or balding scalp from two 14-week, randomized, vehicle-controlled, double-blind studies of imiquimod 3.75% (daily for two 2-week treatment cycles separated by a 2-week treatment-free period) were eligible to enter a 12-month follow-up study if they had no AK lesions at Week 14. Lesion reduction from Lmax was calculated at 6 and 12 months during follow-up.
The 42 patients in this long-term study had a median of nine baseline lesions and a median Lmax of 22 lesions. At 6 and 12 months of follow-up, the median absolute reduction in AK lesions from Lmax with imiquimod 3.75% was 21 and 19, respectively. The median percentage reduction in lesions from Lmax to 6 and 12 months was 100% and 97.2%, respectively.
The ability of imiquimod 3.75% to eliminate clinical and subclinical lesions across an entire sun-exposed field translates into sustained long-term efficacy. Imiquimod 3.75% may therefore represent a first-choice treatment for patients with AK.
在患有光化性角化病(AK)的患者中,亚临床和临床病变同时存在于大面积暴露于阳光下的皮肤中。AK 治疗的长期疗效取决于其清除整个病变区域内这两种类型病变的能力。
评估咪喹莫特 3.75%的长期疗效,通过 Lmax(治疗期间最大病变计数)减少来评估清除亚临床和临床病变的能力。
在两项为期 14 周、随机、安慰剂对照、双盲的咪喹莫特 3.75%(每日一次,连续两个为期 2 周的治疗周期,其间间隔 2 周的治疗间歇期)研究中,有 5-20 个 AK 病变的患者(整个面部或光头头皮)如果在第 14 周时没有 AK 病变,有资格进入为期 12 个月的随访研究。在随访期间的第 6 个月和第 12 个月时,通过 Lmax 计算病变减少。
这项长期研究中的 42 名患者的基线病变中位数为 9 个,Lmax 的中位数为 22 个。在第 6 个月和第 12 个月的随访中,咪喹莫特 3.75%治疗后 Lmax 处 AK 病变的绝对减少中位数分别为 21 和 19。从 Lmax 到第 6 个月和第 12 个月的病变减少百分比中位数分别为 100%和 97.2%。
咪喹莫特 3.75%消除整个暴露于阳光下的区域内临床和亚临床病变的能力转化为持续的长期疗效。因此,咪喹莫特 3.75%可能是 AK 患者的首选治疗方法。