Bradley John S, Orchiston Elaine, Portsmouth Simon, Ariyasu Mari, Baba Takamichi, Katsube Takayuki, Makinde Oluwaseun
From the Department of Pediatrics, University of California, San Diego School of Medicine.
Division of Infectious Diseases, Rady Children's Hospital of San Diego, San Diego, California.
Pediatr Infect Dis J. 2025 Feb 1;44(2):136-142. doi: 10.1097/INF.0000000000004529. Epub 2024 Sep 4.
Multidrug-resistant Gram-negative bacterial infections are increasing globally in neonates, infants and children; antibiotic options are limited.
This international, multicenter, open-label phase 2 study, investigated the pharmacokinetics, safety and tolerability of single-dose and multiple-dose cefiderocol [as a 3-hour infusion (every 8 hours) dosed at 2000 mg for body weight ≥34 kg and at 60 mg/kg for body weight <34 kg], over a range of renal function, in hospitalized pediatric patients with aerobic Gram-negative bacterial infection; multiple-dose patients required standard-of-care systemic antibiotics for 5-14 days. Four cohorts of pediatric patients were enrolled (cohort 1: 12 to <18 years, cohort 2: 6 to <12 years, cohort 3: 2 to <6 years and cohort 4: 3 months to <2 years).
A total of 53 patients (median age: 73.5 months) were enrolled. Plasma concentration profiles were similar with single-dose (n = 24) and multiple-dose (n = 29) cefiderocol, irrespective of age and body weight in those with normal renal function or mild renal impairment. Geometric mean concentrations at the end of infusion ranged between 72.7 and 97.1 μg/mL for single-dose cefiderocol and between 88.8 and 106.0 μg/mL after multiple doses. At 8 hours, corresponding trough concentrations ranged from 7.86 to 10.8 μg/mL with single-dose cefiderocol and from 9.64 to 18.1 μg/mL with multiple doses. There were no deaths, no cefiderocol-related serious adverse events, significant related laboratory abnormalities or discontinuations.
Multiple-dose cefiderocol, administered for 5-14 days and according to body weight, achieved steady-state plasma concentrations that remained above the susceptibility breakpoints of Gram-negative bacteria throughout the dosing period. Cefiderocol was well tolerated.
耐多药革兰氏阴性菌感染在全球范围内的新生儿、婴儿和儿童中呈上升趋势;抗生素选择有限。
这项国际多中心开放标签2期研究,在一系列肾功能水平的住院患有需氧革兰氏阴性菌感染的儿科患者中,研究了单剂量和多剂量头孢地尔(作为3小时输注,体重≥34 kg时剂量为2000 mg,体重<34 kg时剂量为60 mg/kg,每8小时一次)的药代动力学、安全性和耐受性;多剂量组患者需要接受5至14天的标准治疗全身性抗生素。招募了四组儿科患者(第1组:12至<18岁,第2组:6至<12岁,第3组:2至<6岁,第4组:3个月至<2岁)。
共招募了53名患者(中位年龄:73.5个月)。单剂量(n = 24)和多剂量(n = 29)头孢地尔的血浆浓度曲线相似,无论肾功能正常或轻度受损患者的年龄和体重如何。单剂量头孢地尔输注结束时的几何平均浓度在72.7至97.1 μg/mL之间,多剂量后在88.8至106.0 μg/mL之间。在8小时时,单剂量头孢地尔的相应谷浓度在7.86至10.8 μg/mL之间,多剂量在9.64至18.1 μg/mL之间。无死亡病例,无与头孢地尔相关的严重不良事件发生及显著相关实验室异常或停药情况。
多剂量头孢地尔,按体重给药5至14天,在整个给药期间达到的稳态血浆浓度保持在革兰氏阴性菌的药敏断点之上。头孢地尔耐受性良好。