Safety and Efficacy of a 48-Month Efinaconazole 10% Solution Treatment/Maintenance Regimen: 24-Month Daily Use Followed by 24-Month Intermittent Use.

IF 3.4 Q2 INFECTIOUS DISEASES
Aditya K Gupta, Elizabeth A Cooper
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引用次数: 0

Abstract

Background/objectives: In an 18- to 24-month Treatment Phase with once-daily efinaconazole 10% solution, subjects with onychomycosis showed an increased rate of cure at Month 24 versus the phase III trials. In order to further improve efficacy, we initiated an extended intermittent efinaconazole Maintenance Phase with use 2-3 times weekly for an additional 24 months from Month 24 to Month 48. These are the first data presented for a 48-month efinaconazole use period.

Methods: For patients completing 18-24 months of once-daily efinaconazole, the target great toenail from the Treatment Phase was graded as 'Clinical Cure' (≤10% affected area) or 'No Clinical Cure' (>10% affected area) at Month 24. Mycological and clinical outcomes were assessed every 4 months from Month 24 to Month 48. There were 35 patients who enrolled in the extension and continued intermittent efinaconazole use to Month 48. Patients with 'Clinical Cure' at M24 were reviewed for sustained cure at M48; patients with 'No Clinical Cure' were reviewed for development of 'Cure' at M48. All patients were reviewed at all visits for adverse events that may be related to efinaconazole use.

Results: 'Clinical Cure' was found in 6 of 35 enrolled patients at Month 24, and clinical cure status was sustained to Month 48 with intermittent efinaconazole maintenance use. For 29 patients with 'No Clinical Cure', 3/29 achieved 'Clinical Cure' status at Month 48 with intermittent efinaconazole. Effective Cure and Complete Cure rates improved over the maintenance period to Month 48 in subjects without clinical cure at Month 24. Younger patients showed higher cure rates over the maintenance period, but age group cure differences did not reach statistical significance in this dataset, and 49% of the ≥70-year population had at least a 20% reduction in nail area with maintenance therapy to Month 48. There was only 1 case of possible efinaconazole application site reaction in the Intermittent Maintenance Period to Month 48; prolonged efinaconazole use to Month 48 does not appear to increase the risk of reaction. Efinaconazole use periods are associated with very low positive culture rates in this dataset, including typical contaminant organisms, suggesting efinaconazole presence in the nail plate is providing prophylactic therapy.

Conclusions: Intermittent efinaconazole may provide suitable prophylaxis of onychomycosis relapse. Prolonged efinaconazole therapy to Month 48 appears to be safe for all ages and can continue to provide prophylaxis of onychomycosis with Intermittent Maintenance use beyond Month 24 to Month 48.

埃非那康唑10%溶液治疗/维持方案48个月的安全性和有效性:24个月每日使用,随后24个月间歇使用
背景/目的:在18至24个月的治疗阶段,每天一次10%的艾非那康唑溶液,与III期试验相比,甲癣患者在第24个月的治愈率增加。为了进一步提高疗效,我们开始延长间歇性艾非那康唑维持期,从第24个月到第48个月,每周使用2-3次,持续24个月。这是首次提出的48个月艾非康唑使用期的数据。方法:对于完成18-24个月每日一次依非那康唑治疗的患者,治疗阶段的目标大趾甲在第24个月被分级为“临床治愈”(≤10%的患处)或“无临床治愈”(≤10%的患处)。从第24个月至第48个月,每4个月评估一次真菌学和临床结果。有35名患者参加了延长治疗并继续间歇性使用艾非那康唑至第48个月。在M24时“临床治愈”的患者在M48时持续治愈;在M48对“无临床治愈”的患者进行了审查,以开发“治愈”。所有患者在每次就诊时均被复查可能与使用艾非那康唑有关的不良事件。结果:35例入组患者中有6例在第24个月时“临床治愈”,在间歇性使用艾非那康唑维持治疗的情况下,临床治愈状态持续到第48个月。在29例“无临床治愈”的患者中,29例中有3例在第48个月使用间歇性艾非那康唑达到“临床治愈”状态。有效治愈率和完全治愈率在维持期至第48个月期间有所提高,而在第24个月时没有临床治愈的受试者。年轻患者在维持期内的治愈率较高,但年龄组的治愈率差异在本数据集中没有达到统计学意义,49%≥70岁的人群在维持治疗后的第48个月指甲面积至少减少了20%。间断性维持期至第48个月,仅有1例患者可能出现艾非那康唑涂抹部位反应;延长使用艾非那康唑至第48个月似乎不会增加反应的风险。在本数据集中,艾非那康唑的使用周期与非常低的阳性培养率相关,包括典型的污染生物体,这表明艾非那康唑在甲板中的存在提供了预防性治疗。结论:间断性埃非那康唑可有效预防甲真菌病复发。延长艾非那康唑治疗至48个月似乎对所有年龄的患者都是安全的,并且在24个月至48个月后,间歇性维持使用可继续预防甲真菌病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Infectious Disease Reports
Infectious Disease Reports INFECTIOUS DISEASES-
CiteScore
5.10
自引率
0.00%
发文量
82
审稿时长
11 weeks
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