Division of Hygiene and Medical Microbiology, Innsbruck Medical University, Innsbruck, Austria.
Drugs. 2011 Dec 24;71(18):2405-19. doi: 10.2165/11596540-000000000-00000.
Invasive fungal disease continues to be a problem associated with significant morbidity and high mortality in immunocompromised and, to a lesser extent, immunocompetent individuals. Triazole antifungals have emerged as front-line drugs for the treatment and prophylaxis of many systemic mycoses. Fluconazole plays an excellent role in prophylaxis, empirical therapy, and the treatment of both superficial and invasive yeast fungal infections. Voriconazole is strongly recommended for pulmonary invasive aspergillosis. Posaconazole shows a very wide spectrum of activity and its primary clinical indications are as salvage therapy for patients with invasive aspergillosis and prophylaxis for patients with neutropenia and haematopoietic stem-cell transplant recipients. Itraconazole also has a role in the treatment of fungal skin and nail infections as well as dematiaceous fungi and endemic mycoses. Fluconazole and voriconazole are well absorbed and exhibit high oral bioavailability, whereas the oral bioavailability of itraconazole and posaconazole is lower and more variable. Posaconazole absorption depends on administration with a high-fat meal or nutritional supplements. Itraconazole and voriconazole undergo extensive hepatic metabolism involving the cytochrome P450 system. The therapeutic window for triazoles is narrow, and inattention to their pharmacokinetic properties can lead to drug levels too low for efficacy or too high for good tolerability or safety. This makes these agents prime candidates for therapeutic drug monitoring (TDM). Target drug concentrations for voriconazole and itraconazole should be >1 μg/mL and for posaconazole >1.5 μg/mL for treatment. Blood should be drawn once the patient reaches steady state, which occurs after 5 and 7 days of triazole therapy. Routine TDM of fluconazole is not required given its highly favourable pharmacokinetic profile and wide therapeutic index. The aim of this review is to provide a brief update on the pharmacology, activity, clinical efficacy, safety and cost of triazole agents (itraconazole, fluconazole, voriconazole and posaconazole) and highlight the clinical implications of similarities and differences.
侵袭性真菌感染仍然是免疫功能低下者(以及在较小程度上免疫功能正常者)发生重大发病率和高死亡率的相关问题。三唑类抗真菌药物已成为许多全身性真菌感染的一线治疗和预防药物。氟康唑在预防、经验性治疗以及治疗浅表和侵袭性酵母真菌感染方面发挥着出色的作用。伏立康唑强烈推荐用于治疗侵袭性肺曲霉病。泊沙康唑具有非常广泛的活性,其主要临床适应证是作为侵袭性曲霉病患者的挽救治疗和中性粒细胞减少症及造血干细胞移植受者的预防用药。伊曲康唑也可用于治疗真菌性皮肤和指甲感染以及暗色真菌和地方性真菌病。氟康唑和伏立康唑吸收良好,口服生物利用度高,而伊曲康唑和泊沙康唑的口服生物利用度较低且更具变异性。泊沙康唑的吸收取决于与高脂肪餐或营养补充剂同时给药。伊曲康唑和伏立康唑广泛地经肝代谢,涉及细胞色素 P450 系统。三唑类药物的治疗窗较窄,不注意其药代动力学特性可能导致药物水平过低而无法达到疗效,或过高而无法获得良好的耐受性或安全性。这使得这些药物成为治疗药物监测(therapeutic drug monitoring,TDM)的首选候选药物。伏立康唑和伊曲康唑的目标药物浓度应为>1μg/mL,泊沙康唑的目标药物浓度应为>1.5μg/mL 以达到治疗效果。在患者达到稳态后采血,氟康唑稳态一般在氟康唑治疗 5 至 7 天后达到,伊曲康唑和伏立康唑一般在治疗 10 至 14 天后达到。鉴于氟康唑具有极佳的药代动力学特性和较宽的治疗指数,因此不需要常规进行氟康唑 TDM。本综述的目的是简要介绍三唑类药物(伊曲康唑、氟康唑、伏立康唑和泊沙康唑)的药理学、活性、临床疗效、安全性和成本,并强调其相似性和差异性的临床意义。