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每日一次艾氟康唑 10% 溶液(Jublia)治疗皮肤癣菌性趾甲真菌病的长期疗效和安全性:中期分析。

Long-term Efficacy and Safety of Once-daily Efinaconazole 10% Topical Solution (Jublia) for Dermatophyte Toenail Onychomycosis: An Interim Analysis.

机构信息

University of Toronto Department of Medicine, Toronto, ON, Canada.

Mediprobe Research Inc., London, ON, Canada.

出版信息

Skin Therapy Lett. 2021 Jan;26(1):5-10.

Abstract

Onychomycosis, a difficult-to-treat fungal nail infection, is more prevalent in the elderly. Efinaconazole 10% topical solution is a firstline therapy for onychomycosis, based on phase III trials of 12-month treatment; the slow growth of onychomycotic nails suggests a longer treatment period may increase efficacy. This is the first efficacy and safety data for a 24-month duration of efinaconazole 10% topical solution treatment for onychomycosis. Enrolled patients (N = 101) with mild to moderate distal lateral subungual onychomycosis applied efinaconazole to all affected toenails once daily for 18-24 months. Efficacy and safety were evaluated at months 6, 12, 18, and 24 (M6, M12, M18, and M24). The study is ongoing; to date, 47 patients have completed to M24. Mycological cure (MC) was 60.0% at M12, increasing to 74.2% at M24; effective cure (MC and ≤10% clinical involvement of the target toenail) was 17.8% at M12, rising to 19.4% at M24. Mild to moderate application site reactions were the only efinaconazole-related adverse events in 8 patients (7.9%). Increased age, increased severity of onychomycosis, and the presence of mixed infections (dermatophyte plus non-dermatophyte moulds) may drive a need for longer treatment durations. Although the data are interim, there is a trend of increasing efficacy beyond M12 use, without increased safety risk, even in patients >70 years of age.

摘要

甲真菌病,一种难以治疗的真菌感染,在老年人中更为常见。依氟康唑 10%溶液是治疗甲真菌病的一线药物,基于为期 12 个月的 III 期试验;甲真菌病的指甲生长缓慢,表明更长的治疗期可能会提高疗效。这是依氟康唑 10%溶液治疗甲真菌病 24 个月的首次疗效和安全性数据。患有轻度至中度远端侧位甲下甲真菌病的入组患者(N=101)每天应用依氟康唑治疗所有受影响的趾甲一次,治疗 18-24 个月。在第 6、12、18 和 24 个月(M6、M12、M18 和 M24)评估疗效和安全性。该研究正在进行中;迄今为止,已有 47 名患者完成至 M24。第 12 个月时的真菌学治愈率(MC)为 60.0%,至 M24 时增加至 74.2%;第 12 个月时有效治愈率(MC 和 ≤10%目标趾甲的临床受累)为 17.8%,至 M24 时上升至 19.4%。8 名患者(7.9%)出现了轻度至中度的应用部位反应,这是唯一与依氟康唑相关的不良事件。年龄增加、甲真菌病严重程度增加以及混合感染(皮肤癣菌加非皮肤癣菌霉菌)的存在可能需要更长的治疗时间。尽管数据是中期的,但在第 M12 后疗效有增加的趋势,而安全性风险没有增加,即使在>70 岁的患者中也是如此。

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