Medication persistence rates and predictive factors for discontinuation of antifibrotic agents in patients with idiopathic pulmonary fibrosis: a real-world observational study. (August 2019)
- Record Type:
- Journal Article
- Title:
- Medication persistence rates and predictive factors for discontinuation of antifibrotic agents in patients with idiopathic pulmonary fibrosis: a real-world observational study. (August 2019)
- Main Title:
- Medication persistence rates and predictive factors for discontinuation of antifibrotic agents in patients with idiopathic pulmonary fibrosis: a real-world observational study
- Authors:
- Oishi, Keiji
Hirano, Tsunahiko
Murata, Yoriyuki
Hamada, Kazuki
Uehara, Sho
Suetake, Ryo
Yamaji, Yoshikazu
Asami-Noyama, Maki
Edakuni, Nobutaka
Ohata, Syuichiro
Utsunomiya, Toshiaki
Sakamoto, Kenji
Onoda, Hideko
Matsumoto, Tsuneo
Matsunaga, Kazuto
Yano, Masafumi - Abstract:
- Background: In patients with idiopathic pulmonary fibrosis (IPF), continuing treatment with antifibrotic agents is crucial to decrease the reduction of forced vital capacity and mortality rate. However, predictive factors for the discontinuation of antifibrotic agents are unknown. This study aims to investigate the clinical characteristics and predictive factors for the discontinuation of antifibrotic agents in patients with IPF. Methods: This was a double-center retrospective study that enrolled patients with IPF treated with pirfenidone or nintedanib between 2009 and 2017. We compared clinical parameters between the medication-continuing group and the discontinued group. The predictive factors were determined using Cox proportional hazards analyses. Results: A total of 66 subjects were included: 43 received pirfenidone and 23 received nintedanib. At 1 year, 23 of 66 patients had discontinued due to adverse events ( n = 12), disease progression ( n = 9), or death ( n = 2). The characteristics of the discontinuation group were poor performance status (PS) and delay from diagnosis to treatment. In the receiver operating characteristic (ROC) analysis associated with the discontinuation of antifibrotic agents, PS was the highest area under the ROC curve (AUC) value (cut-off value, 2; AUC, 0.83; specificity, 63%; sensitivity, 87%). This finding was consistent even when analyzing, except for examples of death and adjusting for the type of antifibrotic agent. The treatmentBackground: In patients with idiopathic pulmonary fibrosis (IPF), continuing treatment with antifibrotic agents is crucial to decrease the reduction of forced vital capacity and mortality rate. However, predictive factors for the discontinuation of antifibrotic agents are unknown. This study aims to investigate the clinical characteristics and predictive factors for the discontinuation of antifibrotic agents in patients with IPF. Methods: This was a double-center retrospective study that enrolled patients with IPF treated with pirfenidone or nintedanib between 2009 and 2017. We compared clinical parameters between the medication-continuing group and the discontinued group. The predictive factors were determined using Cox proportional hazards analyses. Results: A total of 66 subjects were included: 43 received pirfenidone and 23 received nintedanib. At 1 year, 23 of 66 patients had discontinued due to adverse events ( n = 12), disease progression ( n = 9), or death ( n = 2). The characteristics of the discontinuation group were poor performance status (PS) and delay from diagnosis to treatment. In the receiver operating characteristic (ROC) analysis associated with the discontinuation of antifibrotic agents, PS was the highest area under the ROC curve (AUC) value (cut-off value, 2; AUC, 0.83; specificity, 63%; sensitivity, 87%). This finding was consistent even when analyzing, except for examples of death and adjusting for the type of antifibrotic agent. The treatment persistence rate by PS was PS 0–1 = 90%, PS 2 = 65%, and PS 3 = 19%. Analysis of the relationship between PS and administration period of antifibrotic agents revealed that delays from diagnosis to treatment led to worsening of dyspnea, a decline in lung function, and deterioration of PS. Conclusions: PS may be informative for predicting discontinuation of medication. Our data reinforced the importance of early initiation of antifibrotic treatment, and we suggest PS should be used as a guide for starting antifibrotic agents in everyday practice. The reviews of this paper are available via the supplementary material section. … (more)
- Is Part Of:
- Therapeutic advances in respiratory disease. Volume 13(2019)
- Journal:
- Therapeutic advances in respiratory disease
- Issue:
- Volume 13(2019)
- Issue Display:
- Volume 13, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 13
- Issue:
- 2019
- Issue Sort Value:
- 2019-0013-2019-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-08
- Subjects:
- antifibrotic agents -- drug discontinuation -- early treatment -- IPF -- performance status
Respiratory organs -- Diseases -- Periodicals
Respiratory agents -- Periodicals
Pulmonary pharmacology -- Periodicals
Respiratory Tract Diseases -- Periodicals
Respiratory System Agents -- therapeutic use -- Periodicals
Respiratory Tract Diseases -- drug therapy -- Periodicals
Lung Diseases -- drug therapy -- Periodicals
Appareil respiratoire -- Maladies -- Traitement -- Périodiques
Agents respiratoires -- Périodiques
Pharmacologie pulmonaire -- Périodiques
616.2005 - Journal URLs:
- http://tar.sagepub.com ↗
http://www.uk.sagepub.com/home.nav ↗ - DOI:
- 10.1177/1753466619872890 ↗
- Languages:
- English
- ISSNs:
- 1753-4658
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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