Safety and efficacy of pirfenidone in severe idiopathic pulmonary fibrosis

P. Ntolios, A. Koulelidis, G. Zacharis, A. Tzouvelekis, P. Boglou, K. Kaltsas, E. Bouros, T. Karampitsakos, M. Karailidou, P. Steiropoulos, M. Froudarakis, D. Bouros (Alexandroupolis, Greece)

Source: International Congress 2014 – ILDs 3
Session: ILDs 3
Session type: Thematic Poster Session
Number: 787
Disease area: Interstitial lung diseases

Congress or journal article abstractE-poster

Abstract

Introduction: Pirfenidone is the only, so far, drug approved for the treatment of mild or moderate IPF.Aim: To study the safety and efficacy of pirfenidone in a group of patients with severe disease (FVC<50% and/or TLco < 35%).Methods: Pirfenidone was prescribed to 41 patients with severe IPF. Lung function tests, GAP score and 6 minute walk test (6MWT) were recorded prior and 6 months after treatment initiation. Additionally, patients were strictly monitored with blood tests and liver biochemistry, while adverse events (AE) were recorded and compared to data of previous studies.Results: Mean age was 66.25 ± 12.25. 19.5% were female and 80.5% male. 14.6% had type I respiratory failure. 4.8% had dyspnea MRC I, 22% MRC 2, 39% MRC III, and 34%MRC IV. During the study period 3 patients died from irrelevant to drug causes (1 septic shock, 1 from myocardial infarction and 1 from disease progression) and 7 stopped treatment due to mild-moderate AE. 1 patient stopped for reasons that he did not wish to share. AE included gastro-intestinal discomfort (n=8, 19.5%), photosensitivity (n=5, 12.2%), rash (n=5, 12.2%), fatigue (n=4, 9.75%), diarrhea (n=3, 7.3%), community-acquired pneumonia (n=3, 7.3%), anorexia (n=2, 5%), hematuria (n=2, 4.8%), septic shock (n=2, 4.8%), insomnia, myocardial infarction and irritability one each. No significant differences were observed regarding FVC, TLco, 6MWT, GAP score, SGOT and SGPT pre and 6 months post treatment.Conclusion: Pirfenidone is safe when administered to patients with severe IPF, since AE were comparable to the AZUMA and CAPACITY trials results. Although patients remained stable, longer treatment periods are needed for definite conclusions regarding efficacy.


Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
P. Ntolios, A. Koulelidis, G. Zacharis, A. Tzouvelekis, P. Boglou, K. Kaltsas, E. Bouros, T. Karampitsakos, M. Karailidou, P. Steiropoulos, M. Froudarakis, D. Bouros (Alexandroupolis, Greece). Safety and efficacy of pirfenidone in severe idiopathic pulmonary fibrosis. Eur Respir J 2014; 44: Suppl. 58, 787

You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.

Member's Comments

No comment yet.
You must Login to comment this presentation.


Related content which might interest you:
Predictors of efficacy of pirfenidone in idiopathic pulmonary fibrosis
Source: International Congress 2014 – ILDs 4
Year: 2014


Assessment of telomere length in the combined pulmonary fibrosis and emphysema syndrome
Source: International Congress 2014 – ILDs: diagnostic and prognostic investigations
Year: 2014


Pirfenidone in idiopathic pulmonary fibrosis - description of a German cohort
Source: International Congress 2014 – ILDs 4
Year: 2014


Long term efficacy of pirfenidone therapy in patients with idiopathic pulmonary fibrosis (IPF)
Source: International Congress 2014 – ILDs 3
Year: 2014


Morality predictors in acute exacerbation of idiopathic pulmonary fibrosis
Source: International Congress 2014 – ILDs 6
Year: 2014


Acute exacerbation of idiopathic pulmonary fibrosis: Analysis in a post-marketing surveillance of pirfenidone
Source: International Congress 2014 – Clinical trials in IPF
Year: 2014



Comparison of physiological impairment in ILD patients with and without diagnostic IPF features
Source: International Congress 2014 – ILDs 4
Year: 2014


Proportion of idiopathic pulmonary fibrosis among interstitial lung disease in a tertiary care center and its response to treatment
Source: International Congress 2014 – ILDs 5
Year: 2014


Comparison between patients with idiopathic pulmonary fibrosis and patients with pulmonary involvement of the usual interstitial pneumonia pattern that preceded the onset of rheumatoid arthritis
Source: International Congress 2014 – ILDs: connective tissue disease
Year: 2014

Efficacy and safety of nintedanib in advanced idiopathic pulmonary fibrosis
Source: International Congress 2016 – IPF: from pathogenesis to treatment II
Year: 2016

Prognostic influence of comorbidities in idiopathic pulmonary fibrosis (IPF)
Source: International Congress 2014 – ILDs 2
Year: 2014

Pirfenidone therapy for patients with progressive idiopathic pulmonary fibrosis
Source: International Congress 2014 – ILDs 3
Year: 2014


Clinical features of microscopic polyangiitis with usual interstitial pneumonia-like fibrosis in comparison with idiopathic pulmonary fibrosis
Source: International Congress 2014 – ILDs: connective tissue disease
Year: 2014


Role of midkine in idiopathic pulmonary fibrosis
Source: Annual Congress 2013 –Idiopathic pulmonary fibrosis: clinical view
Year: 2013

Efficacy of pirfenidone in idiopathic pulmonary fibrosis: A single center experience
Source: International Congress 2016 – IPF: from pathogenesis to treatment II
Year: 2016


Transient elastography detection of early liver fibrosis in idiopathic pulmonary fibrosis patients
Source: International Congress 2014 – ILDs 2
Year: 2014


Recent improvement of survival of acute exacerbation in idiopathic interstitial pneumonias: 10 years experience
Source: International Congress 2014 – ILDs 2
Year: 2014

Prognostic significance of selected biomarkers in idiopathic pulmonary fibrosis, sarcoidosis, and chronic pulmonary obstructive disease
Source: International Congress 2014 – Sarcoidosis
Year: 2014


Diffuse dendriform pulmonary ossification in a usual interstitial pneumonia-like distribution: A distinct entity or a variant of idiopathic pulmonary fibrosis?
Source: International Congress 2014 – ILDs 1
Year: 2014


IPFdatabase – A new tool for a correct application of idiopathic pulmonary fibrosis guidelines
Source: International Congress 2014 – ILDs 2
Year: 2014