Naylor M F, Crowson N, Kuwahara R, Teague K, Garcia C, Mackinnis C, Haque R, Odom C, Jankey C, Cornelison R L
Department of Dermatology, St. Johns Hospital, 1923 South Utica Avenue, Tulsa, Oklahoma USA.
Br J Dermatol. 2003 Nov;149 Suppl 66:66-70. doi: 10.1046/j.0366-077x.2003.05637.x.
A published case report and anecdotal experience suggested that topical imiquimod is an effective treatment for stage 0 melanoma (lentigo maligna). To gauge the efficacy of this therapy, we undertook a trial of topical imiquimod in 30 subjects with histologically confirmed lentigo maligna. Thirty subjects with lentigo maligna were recruited for an open-labelled efficacy trial with daily topical application of imiquimod 5% cream for 3 months. Study subjects were enrolled from the Dermatology service of the University of Oklahoma, the Oklahoma City Veteran's Administration Hospital Dermatology service and from referrals for the study from other practitioners. In order to determine an initial response rate, a four-quadrant biopsy was carried out on all patients 1 month after cessation of treatment, targeting the most clinically and dermatoscopically suspicious areas. Of 28 evaluable subjects who have completed the 3-month treatment phase, 26 (93%) were complete responders and two were treatment failures at the time of the 4-quadrant biopsy. Over 80% of the 28 subjects that completed treatment have been followed for more than 1 year with no relapses. The results of this study demonstrate that topical imiquimod produces a high complete response rate in lentigo maligna when applied daily for 3 months.
一篇已发表的病例报告及轶事性经验表明,局部应用咪喹莫特是治疗0期黑色素瘤(恶性雀斑样痣)的有效方法。为评估该疗法的疗效,我们对30例经组织学确诊为恶性雀斑样痣的受试者进行了局部应用咪喹莫特的试验。招募了30例恶性雀斑样痣患者进行一项开放标签的疗效试验,每天局部应用5%咪喹莫特乳膏,持续3个月。研究受试者来自俄克拉荷马大学皮肤科、俄克拉荷马城退伍军人管理局医院皮肤科以及其他从业者推荐参加该研究的患者。为确定初始缓解率,在所有患者停止治疗1个月后进行四象限活检,取材于临床和皮肤镜检查最可疑的区域。在完成3个月治疗阶段的28例可评估受试者中,26例(93%)为完全缓解者,在进行四象限活检时,2例为治疗失败者。完成治疗的28例受试者中,超过80%已随访1年以上,无复发。本研究结果表明,局部应用咪喹莫特每日3个月,对恶性雀斑样痣有较高的完全缓解率。