Gupta Aditya K, Cooper Elizabeth A
Division of Dermatology, Department of Medicine, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 3H2, Canada.
Mediprobe Research Inc., London, ON N5X 2P1, Canada.
Infect Dis Rep. 2025 Jan 13;17(1):7. doi: 10.3390/idr17010007.
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.
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.
'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.
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.
背景/目的:在一项为期18至24个月的治疗阶段,每日一次使用10%艾氟康唑溶液,与III期试验相比,甲癣患者在第24个月时的治愈率有所提高。为了进一步提高疗效,我们启动了一个延长的间歇性艾氟康唑维持阶段,从第24个月到第48个月,每周使用2 - 3次,持续24个月。这是首次呈现的关于艾氟康唑使用48个月的数据。
对于完成18 - 24个月每日一次艾氟康唑治疗的患者,治疗阶段的目标大脚趾指甲在第24个月时被评定为“临床治愈”(感染面积≤10%)或“未临床治愈”(感染面积>10%)。从第24个月到第48个月,每4个月评估一次真菌学和临床结果。有35名患者参加了扩展研究,并持续间歇性使用艾氟康唑至第48个月。对在第24个月时“临床治愈”的患者进行第48个月时持续治愈情况的复查;对“未临床治愈”的患者进行第48个月时“治愈”进展情况的复查。在所有就诊时对所有患者进行与艾氟康唑使用可能相关的不良事件复查。
在第24个月时,35名入组患者中有6名达到“临床治愈”,通过间歇性使用艾氟康唑维持治疗,临床治愈状态持续到第48个月。对于29名“未临床治愈”的患者,其中3/29在第48个月时通过间歇性使用艾氟康唑达到“临床治愈”状态。在第24个月时未临床治愈的受试者中,到第48个月的维持期内有效治愈率和完全治愈率有所提高。年轻患者在维持期内治愈率较高,但在该数据集中年龄组治愈率差异未达到统计学意义,并且在接受维持治疗至第48个月时,≥70岁人群中有49%的指甲面积至少减少了20%。在到第48个月的间歇性维持期内,仅出现1例可能与艾氟康唑应用部位反应相关的病例;将艾氟康唑使用延长至第48个月似乎并未增加反应风险。在该数据集中,艾氟康唑使用期间与包括典型污染物微生物在内的极低阳性培养率相关,表明甲板中存在艾氟康唑可提供预防性治疗。
间歇性使用艾氟康唑可能为甲癣复发提供合适的预防措施。将艾氟康唑治疗延长至第48个月对所有年龄段似乎都是安全的,并且在第24个月至第48个月期间通过间歇性维持使用可继续提供甲癣预防。