Edwards L, Ferenczy A, Eron L, Baker D, Owens M L, Fox T L, Hougham A J, Schmitt K A
Department of Internal Medicine, Carolinas Medical Center, Charlotte, NC 28203, USA.
Arch Dermatol. 1998 Jan;134(1):25-30. doi: 10.1001/archderm.134.1.25.
To compare the safety and effectiveness of 5% and 1% imiquimod cream with vehicle cream in the treatment of external anogenital warts.
Randomized, double-blind, placebo-controlled comparison that evaluated patients for total clearance of their warts. Patients who experienced total clearance were evaluated for recurrence in a 12-week follow-up.
Eleven ambulatory offices, including both private physician offices and referral medical centers.
Three hundred eleven healthy men and women aged 18 years or older with 2 to 50 external anogenital warts were recruited from the practices of investigators, referring physicians, and advertisements. Eighty-two additional patients were screened but did not qualify. Four patients discontinued use of the medication because of adverse effects.
Five percent imiquimod (Aldara) cream, 1% imiquimod cream, or vehicle cream was applied to all external warts overnight 3 times each week for 16 weeks, or until all treated warts disappeared, whichever occurred first.
The number of patients experiencing the elimination of all baseline warts and the recurrence rate of these warts. In addition, the reduction in baseline wart area the duration of therapy required to eliminate warts, and the frequency and severity of adverse reactions were principal measurements.
In the intent-to-treat analysis, 54 (50%) of 109 patients who received 5% imiquimod cream, 21 (21%) of 102 of those who received 1% imiquimod cream, and 11 (11%) of 100 patients treated with vehicle cream experienced eradication of all treated baseline warts. The difference between the effectiveness of 5% imiquimod cream and the vehicle cream was statistically significant (P < .001). Of those patients whose warts cleared during therapy, 13% of patients who received 5% imiquimod experienced a recurrence of at least 1 wart. Recurrences occurred in none of the patients who used 1% imiquimod cream and in 10% of patients who used the vehicle cream. Local erythema was the most common adverse reaction, but the majority of patients in each group experienced no or only mild local inflammatory reactions. There were no differences in incidences of flulike symptoms among treatment groups.
Five percent imiquimod cream is an effective and safe self-administered therapy for external anogenital warts when applied 3 times a week overnight for up to 16 weeks. The recurrence rate is low.
比较5%咪喹莫特乳膏、1%咪喹莫特乳膏与赋形剂乳膏治疗外生殖器肛门疣的安全性和有效性。
随机、双盲、安慰剂对照比较试验,评估患者疣体完全清除情况。疣体完全清除的患者在12周随访期内评估复发情况。
11个门诊办公室,包括私人医生诊所和转诊医疗中心。
从研究者、转诊医生的诊所及广告招募了311名18岁及以上的健康男性和女性,他们有2至50个外生殖器肛门疣。另外82名患者经筛查不符合条件。4名患者因不良反应停药。
5%咪喹莫特(艾达乐)乳膏、1%咪喹莫特乳膏或赋形剂乳膏每周3次每晚涂于所有疣体,持续16周,或直至所有治疗的疣体消失,以先出现者为准。
疣体完全清除的患者数量及这些疣体的复发率。此外,主要观察指标还包括基线疣体面积的减少、疣体清除所需的治疗持续时间以及不良反应的频率和严重程度。
在意向性分析中,接受5%咪喹莫特乳膏治疗的109例患者中有54例(50%)、接受1%咪喹莫特乳膏治疗的102例患者中有21例(21%)、接受赋形剂乳膏治疗的100例患者中有11例(11%)所有治疗的基线疣体均被清除。5%咪喹莫特乳膏与赋形剂乳膏疗效差异有统计学意义(P <.001)。在治疗期间疣体清除的患者中,接受5%咪喹莫特治疗的患者有13%至少复发1个疣体。使用1%咪喹莫特乳膏的患者无复发,使用赋形剂乳膏的患者复发率为10%。局部红斑是最常见的不良反应,但每组大多数患者无或仅有轻度局部炎症反应。各治疗组流感样症状发生率无差异。
5%咪喹莫特乳膏每周3次每晚外用,持续长达16周,是一种治疗外生殖器肛门疣安全有效的自我给药疗法。复发率低。