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Treatment of Idiopathic Pulmonary Fibrosis with Capsule or Tablet Formulations of Pirfenidone in the Real-Life French RaDiCo-ILD Cohort.

Authors :
Cottin, Vincent
Guéguen, Sonia
Nunes, Hilario
Jouneau, Stéphane
Crestani, Bruno
Bonniaud, Philippe
Wemeau, Lidwine
Israël-Biet, Dominique
Reynaud-Gaubert, Martine
Gondouin, Anne
Cadranel, Jacques
Marchand-Adam, Sylvain
Chevereau, Marie
Dufaure-Garé, Isabelle
Amselem, Serge
Clément, Annick
and the RaDiCo team
Bergot, Emmanuel
Bourdin, Arnaud
Chenivesse, Cécile
Source :
Advances in Therapy; Jan2022, Vol. 39 Issue 1, p405-420, 16p
Publication Year :
2022

Abstract

Introduction: Pirfenidone, an antifibrotic medication for idiopathic pulmonary fibrosis (IPF), is now available in France in two formulations: tablets since April 2018, and the initial capsules form. We conducted a cohort study to describe tolerance and acceptability of capsules and/or tablets of pirfenidone in patients with IPF. Methods: This study was nested within the French, non-randomized, multicenter RaDiCo-ILD (Rare Disease Cohort–Interstitial Lung Diseases). Included patients with IPF received at least one dose of pirfenidone tablets or capsules from July 2017 to June 2019 in three populations: the inclusion population (patients treated at least once with pirfenidone during the study period, n = 288); the potential switch population (patients treated with pirfenidone during the switch period starting April 2018, n = 256); the newly treated population (patients who initiated pirfenidone during the study period, n = 162). Each of those last two populations included three subgroups (tablets, capsules, and substitution). Results: In 288 patients treated, 162 newly initiated pirfenidone during the study period: there were no meaningful differences in the baseline characteristics with the 256 patients treated during the potential switch period. In the newly treated population, 30.3% started pirfenidone treatment with tablet formulation. In the potential switch population, 44.9% of patients shifted from capsule to tablet. Half of the patients shifted to tablet formulation within the first 10 months. The mean treatment duration was 21.5 months with a mean dose of 2106.7 mg/day; 46.5% of patients discontinued treatment, mainly because of adverse events. There were fewer discontinuations in the tablets and substitution subgroups than in the capsules-only subgroup. The most reported adverse event was skin rash (11.5%). No new adverse event was identified. Conclusions: This real-life cohort assessing the characteristics of the prescription of pirfenidone tablets and capsules suggests a good acceptability of the tablet formulation by patients with IPF. Trial Registration: Clinical trial registered with www.clinicaltrials.gov (NCT04238871). [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0741238X
Volume :
39
Issue :
1
Database :
Complementary Index
Journal :
Advances in Therapy
Publication Type :
Academic Journal
Accession number :
154979664
Full Text :
https://doi.org/10.1007/s12325-021-01961-x