van der Meer Renske, Wilms Erik B, Heijerman Harry G M
Department of Pulmonology, Haga Teaching Hospital, Els Borst-Eilersplein 275, 2545 AA The Hague, The Netherlands.
Central Hospital Pharmacy, Charlotte Jacobslaan 70, 2545 AB The Hague, The Netherlands.
J Pers Med. 2021 May 24;11(6):458. doi: 10.3390/jpm11060458.
For many people with cystic fibrosis (pwCF), CFTR modulators will be the cornerstone of their treatment. These modulators show robust treatment effects at group level in pwCF with specific mutations. The individual effect however, is variable. In this review we will explain reasons for reconsideration of dosing regimens of CFTR modulating therapy in order to improve treatment response and prevent side effects. Since the effect of a drug depends on pharmacodynamics and pharmacokinetics, pharmacodynamics and pharmacokinetic properties of CFTR modulators will be discussed. Pharmacokinetic-pharmacodynamic relationships will be used to gain insight in dosage response and exposure response relationships. To understand the cause of variation in drug exposure, pharmacokinetic properties that may change due to CF disease will be explained. We show that with current insight, there are conceivable situations that give reason for reconsideration of dosing regimens, however many questions need to be unravelled.
对于许多囊性纤维化患者(pwCF)来说,CFTR调节剂将是他们治疗的基石。这些调节剂在患有特定突变的pwCF患者群体水平上显示出强大的治疗效果。然而,个体效果是可变的。在本综述中,我们将解释重新考虑CFTR调节疗法给药方案的原因,以改善治疗反应并预防副作用。由于药物的效果取决于药效学和药代动力学,因此将讨论CFTR调节剂的药效学和药代动力学特性。药代动力学-药效学关系将用于深入了解剂量反应和暴露反应关系。为了理解药物暴露变化的原因,将解释可能因CF疾病而改变的药代动力学特性。我们表明,根据目前的认识,存在一些可以想象的情况,需要重新考虑给药方案,然而许多问题仍有待解决。