Pharmacological Interactions of Nintedanib and Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis in Times of COVID-19 Pandemic

The discovery of antifibrotic agents have resulted in advances in the therapeutic management of idiopathic pulmonary fibrosis (IPF). Currently, nintedanib and pirfenidone have become the basis of IPF therapy based on the results of large randomized clinical trials showing their safety and efficacy i...

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Main Authors: José M. Serra López-Matencio, Manuel Gómez, Esther F. Vicente-Rabaneda, Miguel A. González-Gay, Julio Ancochea, Santos Castañeda
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Pharmaceuticals
Subjects:
IPF
UIP
Online Access:https://www.mdpi.com/1424-8247/14/8/819
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spelling doaj-5693485fefc14c169a0c2dc41a6c98b42021-08-26T14:12:31ZengMDPI AGPharmaceuticals1424-82472021-08-011481981910.3390/ph14080819Pharmacological Interactions of Nintedanib and Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis in Times of COVID-19 PandemicJosé M. Serra López-Matencio0Manuel Gómez1Esther F. Vicente-Rabaneda2Miguel A. González-Gay3Julio Ancochea4Santos Castañeda5Hospital Pharmacy Service, Princesa Hospital, IIS-Princesa, c/Diego de León 62, 28006 Madrid, SpainMethodology Unit, Health Research Institute Princesa (IIS-IP), c/Diego de León 62, 28006 Madrid, SpainRheumatology Service, Princesa Hospital, IIS-Princesa, c/Diego de León 62, 28006 Madrid, SpainRheumatology Service, Marqués de Valdecilla Universitary Hospital, University of Cantabria, Av. de Valdecilla 25, 39008 Santander, SpainPneumology Service, Princesa Hospital, Autonomous University of Madrid (UAM), IIS-Princesa, c/Diego de León 62, 28006 Madrid, SpainRheumatology Service, Princesa Hospital, IIS-Princesa, c/Diego de León 62, 28006 Madrid, SpainThe discovery of antifibrotic agents have resulted in advances in the therapeutic management of idiopathic pulmonary fibrosis (IPF). Currently, nintedanib and pirfenidone have become the basis of IPF therapy based on the results of large randomized clinical trials showing their safety and efficacy in reducing disease advancement. However, the goal of completely halting disease progress has not been reached yet. Administering nintedanib with add-on pirfenidone is supposed to enhance the therapeutic benefit by simultaneously acting on two different pathogenic pathways. All this becomes more important in the context of the ongoing global pandemic of coronavirus disease 2019 (COVID-19) because of the fibrotic consequences following SARS-CoV-2 infection in some patients. However, little information is available about their drug–drug interaction, which is important mainly in polymedicated patients. The aim of this review is to describe the current management of progressive fibrosing interstitial lung diseases (PF-ILDs) in general and of IPF in particular, focusing on the pharmacokinetic drug-drug interactions between these two drugs and their relationship with other medications in patients with IPF.https://www.mdpi.com/1424-8247/14/8/819antifibrotic agentsCOVID-19interstitial lung diseaseIPFprogressive fibrosing ILDUIP
collection DOAJ
language English
format Article
sources DOAJ
author José M. Serra López-Matencio
Manuel Gómez
Esther F. Vicente-Rabaneda
Miguel A. González-Gay
Julio Ancochea
Santos Castañeda
spellingShingle José M. Serra López-Matencio
Manuel Gómez
Esther F. Vicente-Rabaneda
Miguel A. González-Gay
Julio Ancochea
Santos Castañeda
Pharmacological Interactions of Nintedanib and Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis in Times of COVID-19 Pandemic
Pharmaceuticals
antifibrotic agents
COVID-19
interstitial lung disease
IPF
progressive fibrosing ILD
UIP
author_facet José M. Serra López-Matencio
Manuel Gómez
Esther F. Vicente-Rabaneda
Miguel A. González-Gay
Julio Ancochea
Santos Castañeda
author_sort José M. Serra López-Matencio
title Pharmacological Interactions of Nintedanib and Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis in Times of COVID-19 Pandemic
title_short Pharmacological Interactions of Nintedanib and Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis in Times of COVID-19 Pandemic
title_full Pharmacological Interactions of Nintedanib and Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis in Times of COVID-19 Pandemic
title_fullStr Pharmacological Interactions of Nintedanib and Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis in Times of COVID-19 Pandemic
title_full_unstemmed Pharmacological Interactions of Nintedanib and Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis in Times of COVID-19 Pandemic
title_sort pharmacological interactions of nintedanib and pirfenidone in patients with idiopathic pulmonary fibrosis in times of covid-19 pandemic
publisher MDPI AG
series Pharmaceuticals
issn 1424-8247
publishDate 2021-08-01
description The discovery of antifibrotic agents have resulted in advances in the therapeutic management of idiopathic pulmonary fibrosis (IPF). Currently, nintedanib and pirfenidone have become the basis of IPF therapy based on the results of large randomized clinical trials showing their safety and efficacy in reducing disease advancement. However, the goal of completely halting disease progress has not been reached yet. Administering nintedanib with add-on pirfenidone is supposed to enhance the therapeutic benefit by simultaneously acting on two different pathogenic pathways. All this becomes more important in the context of the ongoing global pandemic of coronavirus disease 2019 (COVID-19) because of the fibrotic consequences following SARS-CoV-2 infection in some patients. However, little information is available about their drug–drug interaction, which is important mainly in polymedicated patients. The aim of this review is to describe the current management of progressive fibrosing interstitial lung diseases (PF-ILDs) in general and of IPF in particular, focusing on the pharmacokinetic drug-drug interactions between these two drugs and their relationship with other medications in patients with IPF.
topic antifibrotic agents
COVID-19
interstitial lung disease
IPF
progressive fibrosing ILD
UIP
url https://www.mdpi.com/1424-8247/14/8/819
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