Literature DB >> 27471208

Efficacy of pirfenidone in patients with idiopathic pulmonary fibrosis with more preserved lung function.

Carlo Albera1, Ulrich Costabel2, Elizabeth A Fagan3, Marilyn K Glassberg4, Eduard Gorina3, Lisa Lancaster5, David J Lederer6, Steven D Nathan7, Dominique Spirig8, Jeff J Swigris9.   

Abstract

This post hoc analysis examined the differences in idiopathic pulmonary fibrosis disease progression and the effects of pirfenidone in patients stratified by more preserved versus less preserved baseline lung function status using forced vital capacity (FVC) or GAP (gender, age and physiology) index stage.Efficacy outcomes, i.e. FVC, 6-min walking distance (6MWD) and dyspnoea (University of California San Diego Shortness of Breath Questionnaire (UCSD SOBQ)), were analysed at 12 months in patients randomised to pirfenidone 2403 mg·day(-1) or placebo in the pooled phase 3 CAPACITY/ASCEND population (n=1247), with subgroups stratified by baseline FVC ≥80% versus <80% or GAP stage I versus II-III. Treatment-by-subgroup interaction was tested based on a rank ANCOVA model; factors in the model included study, region, treatment, subgroup and treatment-by-subgroup interaction term.Patients with both more preserved (FVC ≥80% or GAP stage I) and less preserved (FVC <80% or GAP stage II-III) lung function at baseline demonstrated clinically significant disease progression at 12 months in terms of categorical decline in FVC, 6MWD and UCSD SOBQ. The magnitude of pirfenidone treatment effect was comparable between subgroups, regardless of whether lung function was classified using FVC or GAP index stage.These findings support the initiation of treatment with pirfenidone, irrespective of stage of baseline lung function in this patient population.
Copyright ©ERS 2016.

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Year:  2016        PMID: 27471208     DOI: 10.1183/13993003.01966-2015

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   16.671


  46 in total

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Authors:  Athol U Wells; Maria A Kokosi
Journal:  Am J Respir Crit Care Med       Date:  2016-12-15       Impact factor: 21.405

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3.  Update in Interstitial Lung Disease 2016.

Authors:  Athol U Wells; Toby M Maher
Journal:  Am J Respir Crit Care Med       Date:  2017-07-15       Impact factor: 21.405

Review 4.  Familial Interstitial Lung Disease.

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Review 5.  Idiopathic pulmonary fibrosis: a holistic approach to disease management in the antifibrotic age.

Authors:  Jonathon Shaw; Tracey Marshall; Helen Morris; Conal Hayton; Nazia Chaudhuri
Journal:  J Thorac Dis       Date:  2017-11       Impact factor: 2.895

Review 6.  Progress in Understanding and Treating Idiopathic Pulmonary Fibrosis.

Authors:  Jonathan A Kropski; Timothy S Blackwell
Journal:  Annu Rev Med       Date:  2019-01-27       Impact factor: 13.739

7.  Biomarkers and early treatment of idiopathic pulmonary fibrosis.

Authors:  Jonathan A Kropski
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Review 8.  Managing Idiopathic Pulmonary Fibrosis: Which Drug for Which Patient?

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9.  Pulmonary fibrosis screening: quantifying the psychological impact.

Authors:  Chad A Newton
Journal:  Thorax       Date:  2021-02-23       Impact factor: 9.139

Review 10.  Pirfenidone for Treating Idiopathic Pulmonary Fibrosis: An Evidence Review Group Perspective of a NICE Single Technology Appraisal.

Authors:  Sarah Davis; Rachid Rafia; Christopher Carroll; Jean Hamilton; Munira Essat
Journal:  Pharmacoeconomics       Date:  2019-06       Impact factor: 4.981

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