Suppr超能文献

囊性纤维化跨膜传导调节因子调节剂:一种剂量适用于所有人吗?

CFTR Modulators: Does One Dose Fit All?

作者信息

van der Meer Renske, Wilms Erik B, Heijerman Harry G M

机构信息

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.

出版信息

J Pers Med. 2021 May 24;11(6):458. doi: 10.3390/jpm11060458.

Abstract

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.

摘要

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。

相似文献

1
CFTR Modulators: Does One Dose Fit All?
J Pers Med. 2021 May 24;11(6):458. doi: 10.3390/jpm11060458.
3
CFTR Modulators: The Changing Face of Cystic Fibrosis in the Era of Precision Medicine.
Front Pharmacol. 2020 Feb 21;10:1662. doi: 10.3389/fphar.2019.01662. eCollection 2019.
4
Personalized medicine in CF: from modulator development to therapy for cystic fibrosis patients with rare CFTR mutations.
Am J Physiol Lung Cell Mol Physiol. 2018 Apr 1;314(4):L529-L543. doi: 10.1152/ajplung.00465.2017. Epub 2017 Dec 14.
5
Pharmacokinetics and pharmacodynamics of linezolid in children with cystic fibrosis.
Pediatr Pulmonol. 2009 Feb;44(2):148-54. doi: 10.1002/ppul.20966.
6
Triplet CFTR modulators: future prospects for treatment of cystic fibrosis.
Ther Clin Risk Manag. 2018 Dec 6;14:2375-2383. doi: 10.2147/TCRM.S147164. eCollection 2018.
7
Cystic Fibrosis Transmembrane Regulator Modulators: Implications for the Management of Depression and Anxiety in Cystic Fibrosis.
Psychosomatics. 2017 Jul-Aug;58(4):343-354. doi: 10.1016/j.psym.2017.04.001. Epub 2017 Apr 5.
8
Treating the Underlying Cystic Fibrosis Transmembrane Conductance Regulator Defect in Patients with Cystic Fibrosis.
Semin Respir Crit Care Med. 2019 Dec;40(6):762-774. doi: 10.1055/s-0039-1696664. Epub 2019 Oct 28.
10
Increased extracellular vesicles mediate inflammatory signalling in cystic fibrosis.
Thorax. 2020 Jun;75(6):449-458. doi: 10.1136/thoraxjnl-2019-214027. Epub 2020 Apr 7.

引用本文的文献

5
The Pharmacokinetic Changes in Cystic Fibrosis Patients Population: Narrative Review.
Medicines (Basel). 2024 Dec 31;12(1):1. doi: 10.3390/medicines12010001.
7
Toward better cures for lung disease.
Clin Microbiol Rev. 2024 Dec 10;37(4):e0008023. doi: 10.1128/cmr.00080-23. Epub 2024 Oct 3.
8
Establishment of a conditionally reprogrammed primary eccrine sweat gland culture for evaluation of tissue-specific CFTR function.
J Cyst Fibros. 2024 Nov;23(6):1173-1179. doi: 10.1016/j.jcf.2024.06.013. Epub 2024 Jul 4.

本文引用的文献

1
Airway Epithelial Inflammation Augments the Rescue of Mutant CFTR by Current CFTR Modulator Therapies.
Front Pharmacol. 2021 Mar 30;12:628722. doi: 10.3389/fphar.2021.628722. eCollection 2021.
4
Accumulation and persistence of ivacaftor in airway epithelia with prolonged treatment.
J Cyst Fibros. 2020 Sep;19(5):746-751. doi: 10.1016/j.jcf.2020.04.010. Epub 2020 Jun 11.
5
Effect of CFTR Modulators on Anthropometric Parameters in Individuals with Cystic Fibrosis: An Evidence Analysis Center Systematic Review.
J Acad Nutr Diet. 2021 Jul;121(7):1364-1378.e2. doi: 10.1016/j.jand.2020.03.014. Epub 2020 Jun 10.
6
Personalised medicine for non-classic cystic fibrosis resulting from rare CFTR mutations.
Eur Respir J. 2020 Jul 30;56(1). doi: 10.1183/13993003.00062-2020. Print 2020 Jul.
7
CFTR Modulators: The Changing Face of Cystic Fibrosis in the Era of Precision Medicine.
Front Pharmacol. 2020 Feb 21;10:1662. doi: 10.3389/fphar.2019.01662. eCollection 2019.
8
Variable cellular ivacaftor concentrations in people with cystic fibrosis on modulator therapy.
J Cyst Fibros. 2020 Sep;19(5):742-745. doi: 10.1016/j.jcf.2020.01.011. Epub 2020 Feb 7.
9
Elexacaftor-Tezacaftor-Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele.
N Engl J Med. 2019 Nov 7;381(19):1809-1819. doi: 10.1056/NEJMoa1908639. Epub 2019 Oct 31.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验