Peña-Lorenzo Diego, Rebollo Noemí, Sánchez-Hernández José Germán, Vázquez-López Lourdes, Otero María José, Zarzuelo-Castañeda Aránzazu
Pharmacy Service, University Hospital of Salamanca, 37007 Salamanca, Spain.
Biomedical Research Institute of Salamanca (IBSAL), 37007 Salamanca, Spain.
Life (Basel). 2025 Jun 12;15(6):946. doi: 10.3390/life15060946.
Therapeutic drug monitoring (TDM) is routinely recommended for most antifungal triazoles to ensure efficacy and safety. Isavuconazole, however, was initially approved without this recommendation due to its predictable pharmacokinetic profile. Later clinical data have raised concerns about subtherapeutic exposures in certain populations. This prospective, single-center study aimed to assess the need for TDM of isavuconazole in critically ill and hematologic patients with invasive fungal infections. Between March 2022 and November 2023, patients receiving standard dosing of isavuconazole were enrolled, and plasma concentrations were measured to determine the proportion of patients with values outside the therapeutic range (1-4 µg/mL), particularly focusing on subtherapeutic levels. A total of 65 isavuconazole plasma concentrations from 24 patients (9 critically ill and 15 hematologic) were analyzed. Critically ill patients had lower initial concentrations than hematologic patients (median [range]: 0.75 [not detectable (ND)-5.18] vs. 3.03 [1.03-6.65] µg/mL), with 66.7% showing levels outside the therapeutic range and 55.5% having subtherapeutic concentrations. The coefficient of variation (CV%) of concentrations values at the first TDM was 124.7% in critically ill patients and 57.3% in hematologic patients. After dose adjustment in critically ill patients, the proportion with levels outside the therapeutic range decreased to 28.6%. These findings suggest that, despite initial assumptions, isavuconazole exhibits considerable pharmacokinetic variability in specific populations, particularly in critically ill patients, and the findings support the implementation of TDM to optimize antifungal therapy and improve patient outcomes in real-world clinical settings.
对于大多数抗真菌三唑类药物,常规建议进行治疗药物监测(TDM)以确保疗效和安全性。然而,由于其可预测的药代动力学特征,艾沙康唑最初获批时并未有此建议。后来的临床数据引发了对某些人群中治疗不足暴露情况的担忧。这项前瞻性单中心研究旨在评估侵袭性真菌感染的重症和血液系统疾病患者中艾沙康唑TDM的必要性。在2022年3月至2023年11月期间,纳入接受标准剂量艾沙康唑治疗的患者,并测量血浆浓度以确定治疗范围(1 - 4μg/mL)之外的患者比例,尤其关注治疗不足水平。共分析了24例患者(9例重症患者和15例血液系统疾病患者)的65份艾沙康唑血浆浓度。重症患者的初始浓度低于血液系统疾病患者(中位数[范围]:0.75[未检测到(ND)- 5.18] vs. 3.03[1.03 - 6.65]μg/mL),66.7%的患者浓度超出治疗范围,55.5%的患者浓度处于治疗不足水平。重症患者首次TDM时浓度值的变异系数(CV%)为124.7%,血液系统疾病患者为57.3%。重症患者调整剂量后,超出治疗范围的比例降至28.6%。这些发现表明,尽管有最初的假设,但艾沙康唑在特定人群中,尤其是重症患者中,表现出相当大的药代动力学变异性,这些发现支持在实际临床环境中实施TDM以优化抗真菌治疗并改善患者预后。