Pretreatment rate of decay in forced vital capacity predicts long-term response to pirfenidone in patients with idiopathic pulmonary fibrosis

Autor: Fabrizio Luppi, Marina Saetta, Elisabetta Balestro, Donato Lacedonia, Manuel G. Cosio, Elisabetta Cocconcelli, Stefania Cerri, Maria Pia Foschino Barbaro, Erica Bazzan, Dario Gregori, Paolo Spagnolo, Rosanna Milaneschi, Davide Biondini, Enrico Clini
Přispěvatelé: Biondini, D, Balestro, E, Lacedonia, D, Cerri, S, Milaneschi, R, Luppi, F, Cocconcelli, E, Bazzan, E, Clini, E, Foschino Barbaro, M, Gregori, D, Cosio, M, Saetta, M, Spagnolo, P
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Adult
Male
medicine.medical_specialty
Vital capacity
Pyridones
Vital Capacity
lcsh:Medicine
Rate of decay
Gastroenterology
Article
03 medical and health sciences
Idiopathic pulmonary fibrosis
FEV1/FVC ratio
0302 clinical medicine
forced vital capacity
Internal medicine
idiopathic pulmonary fibrosis
pirfenidone
forced vital capacity

medicine
Humans
In patient
030212 general & internal medicine
Longitudinal Studies
Prospective Studies
lcsh:Science
Aged
Multidisciplinary
idiopathic pulmonary fibrosi
business.industry
Anti-Inflammatory Agents
Non-Steroidal

lcsh:R
Pirfenidone
Middle Aged
respiratory system
medicine.disease
Idiopathic Pulmonary Fibrosis
respiratory tract diseases
Long term response
Treatment Outcome
030228 respiratory system
Disease Progression
Female
lcsh:Q
pirfenidone
business
Progressive disease
medicine.drug
Zdroj: Scientific Reports, Vol 8, Iss 1, Pp 1-7 (2018)
Scientific Reports
Popis: Pirfenidone reduces functional decline in patients with Idiopathic Pulmonary Fibrosis (IPF). However, response to treatment is highly heterogeneous. We sought to evaluate whether response to pirfenidone is influenced by the pretreatment rate of forced vital capacity (FVC) decline. Fifty-six IPF patients were categorized as rapid (RP) or slow progressors (SP) based on whether their FVC decline in the year preceding pirfenidone treatment was > or ≤ 10% predicted. Following pirfenidone treatment patients were followed-up every 6 months and up to 24 months. In the entire population, pirfenidone reduced significantly FVC decline from 231 to 49 ml/year at 6 months (T6) (p = 0.003) and this effect was maintained at the 12-, 18- and 24-month time points (p value for trend n.s.). In RP, the reduction of FVC decline was evident at 6 months (36 vs 706 ml/year pretreatment; p = 0.002) and maintained, though to a lesser degree, at 12 (106 ml/year), 18 (176 ml/year) and 24 months (162 ml/year; p value for trend n.s). Among SP, the reduction in FVC decline was not significant at any of the time points analyzed. In conclusion, pirfenidone reduces FVC decline in IPF patients. However, its beneficial effect is more pronounced in patients with rapidly progressive disease.
Databáze: OpenAIRE