Truong Ngoc Hoa, Benaboud Sihem, Bouazza Naïm, Barboura Mahassen, Bardin Emmanuelle, Miralles Michel, Lui Gabrielle, Froelicher-Bournaud Léo, Rouillon Steeve, Bihouee Tiphaine, Bui Stéphanie, Reix Philippe, Dalphin Marie-Laure, Laurans Muriel, Languepin Jeanne, Corvol Harriet, Troussier Françoise, Weiss Laurence, Cinthia Rames, Tatopoulos Aurélie, Deneuville Eric, Chiron Raphael, Stremler Nathalie, Llerena Cathy, Ramel Sophie, Perisson Caroline, Houdoin Véronique, Mittaine Marie, Treluyer Jean-Marc, Sermet-Gaudelus Isabelle, Foissac Frantz
Pharmacologie et Évaluations des Thérapeutiques Chez L'Enfant et la Femme Enceinte, Université Paris Cité, Inserm, Paris, France.
Service de Pharmacologie Clinique, Hôpital Cochin, AP-HP, Université Paris Cité, Paris, France.
Clin Transl Sci. 2025 May;18(5):e70245. doi: 10.1111/cts.70245.
Elexacaftor/tezacaftor/ivacaftor (ETI) significantly improves treatment outcomes for people with cystic fibrosis (pwCF) with at least one F508del allele. In 2023, the Food and Drug Administration approved ETI for children with CF aged 2-5 years. However, real-world pharmacokinetic-pharmacodynamic data for ETI in pediatric and adult populations are still limited. This study aimed to characterize the population PK of ETI in children with CF (chCF) and evaluate current dosing recommendations. Population PK modeling was conducted using Monolix software on 150 ETI concentrations obtained from therapeutic drug (TDM) monitoring in 96 children with CF aged 2-18 years, as part of the MODUL-CF study. Area under the curve was derived from individual Bayesian pharmacokinetic estimates. A one-compartment model with a lag time, first-order absorption, and elimination best described the PK of elexacaftor/ivacaftor, while the PK of tezacaftor followed a one-compartment model with first-order absorption and elimination. A large between-subject variability was observed. The effect of body weight was significant on apparent clearance and volume of distribution parameters using allometric scaling. Children weighing 30-40 kg who received the adult-recommended dose showed higher drug exposure compared to adults with cystic fibrosis. This is the first study to describe the population pharmacokinetics of ETI in chCF aged 2-18 years, revealing high between-subject variability for all three drugs. In this context, TDM is likely essential for managing ETI exposure levels and guiding dosing adjustments. The appropriateness of current dosing recommendations for children under 12 years old weighing 30-40 kg remains to be clarified.
依列卡福妥/替扎卡福妥/依伐卡托(ETI)可显著改善至少携带一个F508del等位基因的囊性纤维化患者(pwCF)的治疗效果。2023年,美国食品药品监督管理局批准ETI用于2至5岁的囊性纤维化儿童。然而,ETI在儿科和成人人群中的真实世界药代动力学-药效学数据仍然有限。本研究旨在描述ETI在囊性纤维化儿童(chCF)中的群体药代动力学特征,并评估当前的给药建议。作为MODUL-CF研究的一部分,使用Monolix软件对96名2至18岁囊性纤维化儿童治疗药物监测(TDM)获得的150个ETI浓度进行群体药代动力学建模。曲线下面积来自个体贝叶斯药代动力学估计值。具有滞后时间、一级吸收和消除的单室模型最能描述依列卡福妥/依伐卡托的药代动力学,而替扎卡福妥的药代动力学遵循具有一级吸收和消除的单室模型。观察到较大的个体间变异性。使用异速生长标度法,体重对表观清除率和分布容积参数有显著影响。体重30至40公斤且接受成人推荐剂量的儿童与患有囊性纤维化的成人相比,药物暴露量更高。这是第一项描述2至18岁chCF中ETI群体药代动力学的研究,揭示了所有三种药物都有较高的个体间变异性。在此背景下,TDM可能对于管理ETI暴露水平和指导剂量调整至关重要。目前针对体重30至40公斤的12岁以下儿童的给药建议是否合适仍有待明确。