Department of Infectious Disease, Cleveland Clinic, Cleveland, Ohio.
Department of Pharmacy, Cleveland Clinic, Cleveland, Ohio.
Mycoses. 2019 Jun;62(6):534-541. doi: 10.1111/myc.12910. Epub 2019 Mar 28.
Isavuconazole use in the real-world setting has not been extensively described. Subgroups of patients with particular prognostic significance, such as previous triazole prophylaxis or treatment and the important subgroup treated empirically for invasive fungal infection, have beforehand been excluded from trials.
We aimed to determine treatment response and safety in these patients at a large US transplant and cancer centre.
PATIENTS/METHODS: We conducted a retrospective cohort study of all adult inpatients administered ≥3 doses of isavuconazole between June 2015 and October 2017.
Ninety-one adults were identified. Six (7%) received primary prophylaxis, 10 (11%) treatment then secondary prophylaxis and 75 (82%) treatment only. Overall treatment response was 62%. Six-week mortality was 24%. Sixty-three per cent of 32 patients treated with isavuconaozle following prophylaxis with another antifungal agent exhibited a treatment response. Among 49 patients switched from treatment with another agent, 53% had a treatment response. Thirty-four patients received isavuconazole empirically, and 65% demonstrated a treatment response. Individuals given isavuconazole prophylaxis developed no breakthrough invasive fungal infections. One patient discontinued isavuconazole due to hepatotoxicity.
Real-world isavuconazole use appears safe and is associated with treatment responses in varied patients including critically important subgroups previously unreported.
伊曲康唑在真实环境中的应用尚未得到广泛描述。先前的试验排除了具有特定预后意义的患者亚组,例如先前的三唑类预防用药或治疗以及重要的经验性治疗侵袭性真菌感染的亚组。
我们旨在确定大型美国移植和癌症中心的这些患者的治疗反应和安全性。
患者/方法:我们对 2015 年 6 月至 2017 年 10 月期间接受至少 3 剂伊曲康唑治疗的所有成年住院患者进行了回顾性队列研究。
确定了 91 名成年人。6 人(7%)接受了原发性预防,10 人(11%)治疗后接受了继发性预防,75 人(82%)仅接受了治疗。总体治疗反应为 62%。6 周死亡率为 24%。在接受另一种抗真菌药物预防治疗的 32 名患者中,有 63%的患者治疗反应良好。在 49 名从另一种药物转换治疗的患者中,有 53%的患者治疗反应良好。34 名患者接受伊曲康唑经验性治疗,65%的患者治疗反应良好。接受伊曲康唑预防的患者未发生突破性侵袭性真菌感染。1 名患者因肝毒性而停止使用伊曲康唑。
真实世界中使用伊曲康唑似乎是安全的,并与各种患者的治疗反应相关,包括以前未报道过的重要亚组。