Pharmaceutical Sciences Postgraduate Program, Federal University of Paraná, Curitiba, Brazil.
Pharmaceutical Sciences Postgraduate Program, Federal University of Paraná, Curitiba, Brazil; H&TRC- Health & Technology Research Center, ESTeSL- Escola Superior de Tecnologia da Saúde, Instituto Politécnico de Lisboa, Lisbon, Portugal.
Int J Antimicrob Agents. 2022 Aug;60(2):106614. doi: 10.1016/j.ijantimicag.2022.106614. Epub 2022 Jun 9.
Invasive candidiasis is the most common fungal infection in patients attending health services and is associated with high mortality rates and prolonged hospital stay. The aim of this review was to evaluate and compare efficacy and safety of antifungal agents for the treatment of candidemia.
A systematic review with network meta-analysis (NMA), surface under the cumulative ranking analysis (SUCRA) and stochastic multicriteria acceptability analyses (SMAA) was performed (PROSPERO-CRD42020149264). Searches were conducted in PubMed and Scopus (Nov-2021). Randomised controlled trials evaluating the effect of oral antifungals (any dose or regimen) on mycological cure, discontinuation rates and adverse events were included.
Overall, 13 trials (n=3632) were analysed. There were no significant differences between therapies for the efficacy outcomes; however, caspofungin (50-150 mg), rezafungin (200-400 mg) and micafungin (100-150 mg) had higher rates of clinical and mycological responses (SUCRA overall response >60%) and were considered the most promising therapies. Fluconazole (400 mg) rated worst for overall response (17%). Rezafungin (200-400 mg) and micafungin (100 mg) were associated with lower discontinuation rates (<40%). Conventional amphotericin B (0.6-0.7 mg/kg) was more likely to be discontinued (odds ratio [OR] 0.08; 95% credibility interval [CrI] 0.00-0.95 vs. caspofungin 150 mg) and may impair liver function (87%).
Echinocandins are recommended as first-line treatments for invasive candidiasis following a priority order of caspofungin then micafungin. Rezafungin, an echinocandin under development, represents a potential option that should be further investigated. Azoles and liposomal amphotericin B can be used as second-line treatments in cases of fungal resistance or hypersensitivity.
侵袭性念珠菌病是在医疗机构就诊的患者中最常见的真菌感染,与高死亡率和延长住院时间有关。本研究旨在评估和比较抗真菌药物治疗念珠菌血症的疗效和安全性。
进行了一项系统评价,采用网络荟萃分析(NMA)、累积排序曲线下面积(SUCRA)和随机多标准接受性分析(SMAA)进行分析(PROSPERO-CRD42020149264)。检索了 PubMed 和 Scopus(2021 年 11 月)。纳入了评估口服抗真菌药物(任何剂量或方案)对真菌学治愈率、停药率和不良事件影响的随机对照试验。
共分析了 13 项试验(n=3632)。在疗效结果方面,各种治疗方法之间没有显著差异;然而,卡泊芬净(50-150mg)、瑞他康唑(200-400mg)和米卡芬净(100-150mg)的临床和真菌学反应率更高(总体反应 SUCRA>60%),被认为是最有前途的治疗方法。氟康唑(400mg)的总体反应最差(17%)。瑞他康唑(200-400mg)和米卡芬净(100mg)停药率较低(<40%)。常规两性霉素 B(0.6-0.7mg/kg)更有可能停药(比值比[OR]0.08;95%可信度区间[CrI]0.00-0.95 vs. 卡泊芬净 150mg),并且可能损害肝功能(87%)。
棘白菌素类药物被推荐为侵袭性念珠菌病的一线治疗药物,按卡泊芬净和米卡芬净的优先级顺序排列。瑞他康唑是一种正在开发的棘白菌素类药物,可能是一种有前途的选择,应进一步研究。唑类药物和脂质体两性霉素 B 可作为真菌耐药或过敏时的二线治疗药物。