Weiner Marc, Savic Radojka M, Kenzie William R Mac, Wing Diane, Peloquin Charles A, Engle Melissa, Bliven Erin, Prihoda Thomas J, Gelfond Jonathan A L, Scott Nigel A, Abdel-Rahman Susan M, Kearns Gregory L, Burman William J, Sterling Timothy R, Villarino M Elsa
Department of Medicine, University of Texas Health Science Center, San Antonio Veterans Administration Medical Center, San Antonio, Texas.
University of California at San Francisco, School of Pharmacy, Bioengineering and Therapeutic Sciences.
J Pediatric Infect Dis Soc. 2014 Jun;3(2):132-45. doi: 10.1093/jpids/pit077. Epub 2014 Jan 16.
In a phase 3, randomized clinical trial (PREVENT TB) of 8053 people with latent tuberculosis infection, 12 once-weekly doses of rifapentine and isoniazid had good efficacy and tolerability. Children received higher rifapentine milligram per kilogram doses than adults. In the present pharmacokinetic study (a component of the PREVENT TB trial), rifapentine exposure was compared between children and adults.
Rifapentine doses in children ranged from 300 to 900 mg, and adults received 900 mg. Children who could not swallow tablets received crushed tablets. Sparse pharmacokinetic sampling was performed with 1 rifapentine concentration at 24 hours after drug administration (C24). Rifapentine area under concentration-time curve (AUC) was estimated from a nonlinear, mixed effects regression model (NLME).
There were 80 children (age: median, 4.5 years; range, 2-11 years) and 77 adults (age: median, 40 years; all ≥18 years) in the study. The geometric mean rifapentine milligram per kilogram dose was greater in children than in adults (children, 23 mg/kg; adults, 11 mg/kg). Rifapentine geometric mean AUC and C24 were 1.3-fold greater in children (all children combined) than in adults. Children who swallowed whole tablets had 1.3-fold higher geometric mean AUC than children who received crushed tablets, and children who swallowed whole tablets had a 1.6-fold higher geometric mean AUC than adults. The higher rifapentine doses in children were well tolerated. To obtain rifapentine exposures comparable in children to adults, dosing algorithms modeled by NLME were developed.
A 2-fold greater rifapentine dose for all children resulted in a 1.3-fold higher AUC compared to adults administered a standard dose. Use of higher weight-adjusted rifapentine doses for young children are warranted to achieve systemic exposures that are associated with successful treatment of latent tuberculosis infection in adults.
在一项针对8053名潜伏性结核感染患者的3期随机临床试验(预防结核病试验)中,每周一次服用12剂利福喷汀和异烟肼具有良好的疗效和耐受性。儿童每公斤体重服用的利福喷汀剂量高于成人。在本药代动力学研究(预防结核病试验的一个组成部分)中,对儿童和成人的利福喷汀暴露情况进行了比较。
儿童的利福喷汀剂量范围为300至900毫克,成人为900毫克。无法吞服片剂的儿童服用碾碎的片剂。在给药后24小时进行稀疏药代动力学采样,测定1个利福喷汀浓度(C24)。利福喷汀浓度-时间曲线下面积(AUC)通过非线性混合效应回归模型(NLME)估算。
研究中有80名儿童(年龄中位数为4.5岁;范围为2至11岁)和77名成人(年龄中位数为40岁;均≥18岁)。儿童每公斤体重利福喷汀剂量的几何平均值高于成人(儿童为23毫克/千克;成人 为11毫克/千克)。儿童(所有儿童合并计算)的利福喷汀几何平均AUC和C24比成人高1.3倍。吞服整片的儿童的几何平均AUC比服用碾碎片剂的儿童高1.3倍,吞服整片的儿童的几何平均AUC比成人高1.6倍。儿童服用较高剂量的利福喷汀耐受性良好。通过NLME建立了给药算法模型,以使儿童的利福喷汀暴露量与成人相当。
所有儿童服用的利福喷汀剂量增加1倍,与服用标准剂量的成人相比,AUC高1.3倍。对于幼儿,有必要使用更高的按体重调整的利福喷汀剂量,以实现与成人潜伏性结核感染成功治疗相关的全身暴露量。