Gupta Samir K, Glue Paul, Jacobs Sheila, Belle Donna, Affrime Melton
Schering-Plough Research Institute, Kenilworth, NJ 07033, USA.
Br J Clin Pharmacol. 2003 Jul;56(1):131-4. doi: 10.1046/j.1365-2125.2003.01836.x.
To assess the single-dose pharmacokinetics and tolerability of pegylated interferon-alpha2b (PEG-Intron) in young and elderly healthy subjects.
In this parallel-design study, a single 1 microg x kg(-1) PEG-Intron dose was given subcutaneously to 24 subjects in the age groups 20-45, 65-69, 70-74 and 75-80 years (n = 6/group). Blood sampling and tolerability assessments were performed up to 168 h postdose.
The pharmacokinetic parameters were similar in all age groups. The elderly to young subject ratios for Cmax were 91.1, 79.5, and 107% for the 65-69 years, 70-74 years and 75-80 years groups, respectively. The corresponding values for AUC(0- infinity ) and CL/F were 111, 102 and 108%, and 82.5, 95.8 and 86.4%, respectively. Mean differences from the 20 to 45 years group and the 65-69 years, 70-74 years and 75-80 years groups for PEG-Intron Vd/F were 108, 128 and 104%, respectively. None of these differences was statistically significant based on ANOVA. Results from a Dunnett's test (as post hoc assessment) confirmed that the pharmacokinetic parameters of Group II, Group III or Group IV were not different from those of Group I. Almost all (23/24; 96%) subjects reported typical interferon-alpha side-effects (flu-like symptoms, headache). One elderly patient had a myocardial infarction 12 h postdose, but recovered fully.
There are no pharmacokinetic reasons for initial dose adjustment of PEG-Intron based on age.
评估聚乙二醇化干扰素-α2b(派罗欣)在年轻和老年健康受试者中的单剂量药代动力学及耐受性。
在这项平行设计研究中,对年龄分别为20 - 45岁、65 - 69岁、70 - 74岁和75 - 80岁的24名受试者(每组6人)皮下给予单次1μg·kg⁻¹的派罗欣剂量。给药后168小时内进行血样采集和耐受性评估。
所有年龄组的药代动力学参数相似。65 - 69岁、70 - 74岁和75 - 80岁组的老年受试者与年轻受试者的Cmax比值分别为91.1%、79.5%和107%。AUC(0 - ∞)和CL/F的相应值分别为111%、102%和108%,以及82.5%、95.8%和86.4%。派罗欣Vd/F在20 - 45岁组与65 - 69岁、70 - 74岁和75 - 80岁组的平均差异分别为108%、128%和104%。基于方差分析,这些差异均无统计学意义。Dunnett检验(作为事后评估)结果证实,第二组、第三组或第四组的药代动力学参数与第一组无差异。几乎所有(23/24;96%)受试者报告了典型的干扰素-α副作用(流感样症状、头痛)。一名老年患者在给药后12小时发生心肌梗死,但完全康复。
不存在基于年龄对派罗欣初始剂量进行调整的药代动力学原因。