Wilson Dustin T, Dimondi V Paul, Johnson Steven W, Jones Travis M, Drew Richard H
Department of Pharmacy Practice, Campbell University College of Pharmacy & Health Sciences, Buies Creek, NC, USA; Department of Pharmacy, Duke University Hospital, Durham, NC, USA.
Department of Pharmacy Practice, Campbell University College of Pharmacy & Health Sciences, Buies Creek, NC, USA; Department of Pharmacy, Durham VA Medical Center, Durham, NC, USA.
Ther Clin Risk Manag. 2016 Aug 3;12:1197-206. doi: 10.2147/TCRM.S90335. eCollection 2016.
Despite recent advances in both diagnosis and prevention, the incidence of invasive fungal infections continues to rise. Available antifungal agents to treat invasive fungal infections include polyenes, triazoles, and echinocandins. Unfortunately, individual agents within each class may be limited by spectrum of activity, resistance, lack of oral formulations, significant adverse event profiles, substantial drug-drug interactions, and/or variable pharmacokinetic profiles. Isavuconazole, a second-generation triazole, was approved by the US Food and Drug Administration in March 2015 and the European Medicines Agency in July 2015 for the treatment of adults with invasive aspergillosis (IA) or mucormycosis. Similar to amphotericin B and posaconazole, isavuconazole exhibits a broad spectrum of in vitro activity against yeasts, dimorphic fungi, and molds. Isavuconazole is available in both oral and intravenous formulations, exhibits a favorable safety profile (notably the absence of QTc prolongation), and reduced drug-drug interactions (relative to voriconazole). Phase 3 studies have evaluated the efficacy of isavuconazole in the management of IA, mucormycosis, and invasive candidiasis. Based on the results of these studies, isavuconazole appears to be a viable treatment option for patients with IA as well as those patients with mucormycosis who are not able to tolerate or fail amphotericin B or posaconazole therapy. In contrast, evidence of isavuconazole for invasive candidiasis (relative to comparator agents such as echinocandins) is not as robust. Therefore, isavuconazole use for invasive candidiasis may initially be reserved as a step-down oral option in those patients who cannot receive other azoles due to tolerability or spectrum of activity limitations. Post-marketing surveillance of isavuconazole will be important to better understand the safety and efficacy of this agent, as well as to better define the need for isavuconazole serum concentration monitoring.
尽管在诊断和预防方面取得了最新进展,但侵袭性真菌感染的发病率仍在持续上升。用于治疗侵袭性真菌感染的现有抗真菌药物包括多烯类、三唑类和棘白菌素类。不幸的是,每一类中的个别药物可能受到活性谱、耐药性、缺乏口服制剂、显著的不良事件谱、大量的药物相互作用和/或可变的药代动力学谱的限制。艾沙康唑是一种第二代三唑类药物,于2015年3月获得美国食品药品监督管理局批准,并于2015年7月获得欧洲药品管理局批准,用于治疗患有侵袭性曲霉病(IA)或毛霉病的成人。与两性霉素B和泊沙康唑类似,艾沙康唑在体外对酵母、双相真菌和霉菌具有广泛的活性谱。艾沙康唑有口服和静脉制剂,具有良好的安全性(特别是不存在QTc延长),并减少了药物相互作用(相对于伏立康唑)。3期研究评估了艾沙康唑在IA、毛霉病和侵袭性念珠菌病管理中的疗效。基于这些研究的结果,艾沙康唑似乎是IA患者以及那些不能耐受或对两性霉素B或泊沙康唑治疗无效的毛霉病患者的可行治疗选择。相比之下,艾沙康唑用于侵袭性念珠菌病(相对于棘白菌素等对照药物)的证据并不那么充分。因此,艾沙康唑用于侵袭性念珠菌病最初可保留为那些因耐受性或活性谱限制而无法接受其他唑类药物的患者的降阶梯口服选择。对艾沙康唑进行上市后监测对于更好地了解该药物的安全性和疗效,以及更好地确定监测艾沙康唑血清浓度的必要性将非常重要。