Population Pharmacokinetics and Exposure-Response Relationship of Hemoporfin in Pediatric Patients With Port-Wine Stain.

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Rong Chen, Bin Zhang, Jining Tao, Qingyu Yao, Tianyan Zhou, Lin Ma, Zigang Xu
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Abstract

Hemoporfin, a porphyrin derivative photosensitizer, has been approved for the treatment of port-wine stain (PWS) in adults. However, its optimal dose for the pediatric population remains unclear. This study aimed to explore appropriate dosing for pediatric patients with PWS through population pharmacokinetics (PopPK) and exposure-response (ER) analysis. Data from a prospective pilot study of hemoporfin photodynamic therapy in pediatric PWS patients, as well as a phase I study in healthy adult volunteers, were utilized for the analysis. The pharmacokinetics of hemoporfin in the pediatric population can be described by a three-compartment model with linear elimination following allometric scaling rules. Simulations indicated that simply scaling down the approved adult dose of 5 mg/kg based on weight for the pediatric population, which is a common practice among clinicians, may lead to reduced drug exposure in pediatric patients. Mean Cmax and AUC0-30min in pediatric patients were 18.7% and 30.5% lower than those in adults, respectively. A positive relationship was identified between AUC0-30min and the probability of investigators or patients giving high ratings for efficacy, suggesting that improved efficacy may be achieved with higher hemoporfin exposure. A series of dosing regimens were explored to match exposure in the pediatric population to that of the adult population. These findings may accelerate the development of pediatric indications for hemoporfin and help address the unmet medical needs of pediatric patients with PWS.

儿童波特酒染色患者血红蛋白的人群药动学及暴露-反应关系。
Hemoporfin是一种卟啉衍生物光敏剂,已被批准用于治疗成人波特酒斑(PWS)。然而,其对儿童人群的最佳剂量仍不清楚。本研究旨在通过人群药代动力学(PopPK)和暴露-反应(ER)分析,探讨小儿PWS患者的适当剂量。本研究的数据来自一项针对儿科PWS患者的光动力治疗的前瞻性先导研究,以及一项针对健康成人志愿者的I期研究。在儿童人群中,血红蛋白的药代动力学可以用一个三室模型来描述,该模型具有线性消除,遵循异速缩放规则。模拟结果表明,临床医生的常见做法是,简单地根据儿童的体重减少批准的成人剂量5mg /kg,这可能会减少儿童患者的药物暴露。儿童患者的平均Cmax和AUC0-30min分别比成人低18.7%和30.5%。研究发现,AUC0-30min与研究者或患者对疗效给予高评分的概率呈正相关,表明较高的血孔蛋白暴露可能会提高疗效。研究人员探索了一系列的给药方案,以使儿科人群的暴露与成人人群的暴露相匹配。这些发现可能会加速儿童血液疏松症适应症的发展,并有助于解决PWS儿童患者未满足的医疗需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.00
自引率
11.40%
发文量
146
审稿时长
8 weeks
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