Mediprobe Research Inc., London, ON, Canada.
Division of Dermatology, Department of Medicine, University of Toronto School of Medicine, Toronto, ON, Canada.
Br J Dermatol. 2023 Jul 7;189(1):12-22. doi: 10.1093/bjd/ljad070.
There is a paucity of evidence regarding the relative therapeutic efficacy of treatments for onychomycosis.
We determined the relative efficacy of monotherapies for dermatophyte toenail onychomycosis with Bayesian network meta-analyses (NMAs).
We searched PubMed, Scopus, EMBASE (Ovid) and CINAHL to identify studies that investigated the efficacy of monotherapy with oral antifungals for dermatophyte toenail onychomycosis in adults. In this paper, 'regimen' corresponds to a given agent and its dosage. The relative effects and surface under the cumulative ranking curve (SUCRA) values of the various regimens were estimated; evidence quality was assessed at the study level and across networks.
Data from 21 studies were used. Our two efficacy-related endpoints were: (i) mycological and (ii) complete cure at 1 year; safety--related endpoints were: (i) 1-year count of any adverse event (AE), (ii) 1-year odds of discontinuation due to any AE, (iii) 1-year odds of discontinuation due to liver issues. Thirty-five regimens were identified; the newer agents among these included posaconazole and oteseconazole. We compared the efficacy of newer regimens with traditional ones like 'terbinafine 250 mg daily for 12 weeks' and 'itraconazole 200 mg daily for 12 weeks. We found that an agent's dosage was associated with its efficacy; for example, the 1-year odds of mycological cure with terbinafine 250 mg daily for 24 weeks (SUCRA = 92.4%) were significantly greater than those of terbinafine 250 mg daily for 12 weeks (SUCRA = 66.3%) (odds ratio 2.62, 95% credible interval 1.57-4.54). We also found that booster regimens can increase efficacy. Our results showed that some triazoles could be more effective than terbinafine.
This is the first NMA study of monotherapeutic antifungals - and their various dosages - for dermatophyte toenail onychomycosis. Our findings could provide guidance for the selection of the most appropriate antifungal agent, especially amid the growing concerns about terbinafine resistance.
关于治疗甲真菌病的相对疗效,证据有限。
我们通过贝叶斯网络荟萃分析(NMA)确定了治疗真菌性趾甲甲真菌病的单药治疗的相对疗效。
我们检索了 PubMed、Scopus、EMBASE(Ovid)和 CINAHL,以确定研究成人使用口服抗真菌药单药治疗真菌性趾甲甲真菌病疗效的研究。在本文中,“方案”对应于特定药物及其剂量。估计了各种方案的相对效果和累积排序曲线下面积(SUCRA)值;在研究水平和网络层面评估了证据质量。
使用了 21 项研究的数据。我们的两个疗效相关终点是:(i)真菌学和(ii)1 年完全治愈;安全性相关终点是:(i)1 年任何不良事件(AE)的发生率,(ii)1 年因任何 AE 停药的可能性,(iii)1 年因肝脏问题停药的可能性。确定了 35 种方案;其中较新的药物包括泊沙康唑和奥昔康唑。我们比较了新方案与传统方案(如“特比萘芬 250mg 每日,疗程 12 周”和“伊曲康唑 200mg 每日,疗程 12 周”)的疗效。我们发现,药物剂量与疗效相关;例如,特比萘芬 250mg 每日,疗程 24 周的 1 年真菌学治愈率(SUCRA = 92.4%)明显高于特比萘芬 250mg 每日,疗程 12 周(SUCRA = 66.3%)(比值比 2.62,95%置信区间 1.57-4.54)。我们还发现,强化方案可以提高疗效。我们的研究结果表明,一些三唑类药物可能比特比萘芬更有效。
这是第一项关于治疗真菌性趾甲甲真菌病的单药治疗(及其各种剂量)的 NMA 研究。我们的研究结果可以为选择最合适的抗真菌药物提供指导,特别是在人们对特比萘芬耐药性日益关注的情况下。