Detailed Information on Publication Record
2023
The effect of nintedanib on lung functions and survival in idiopathic pulmonary fibrosis: real-life analysis of the Czech EMPIRE registry
STEFANIKOVA, Marianna, Martina DOUBKOVÁ, Petra OVESNÁ, Martina STERCLOVA, Ladislav LACINA et. al.Basic information
Original name
The effect of nintedanib on lung functions and survival in idiopathic pulmonary fibrosis: real-life analysis of the Czech EMPIRE registry
Authors
STEFANIKOVA, Marianna (203 Czech Republic, guarantor), Martina DOUBKOVÁ (203 Czech Republic, belonging to the institution), Petra OVESNÁ (203 Czech Republic, belonging to the institution), Martina STERCLOVA (203 Czech Republic), Ladislav LACINA (203 Czech Republic), Monika ZURKOVA (203 Czech Republic), Martina PLACKOVA (203 Czech Republic), Vladimir BARTOS (203 Czech Republic), Ivana JANICKOVA (203 Czech Republic), Radka BITTENGLOVA (203 Czech Republic), Jan ANTON (203 Czech Republic), Lubica SÝKOROVÁ (703 Slovakia, belonging to the institution), Vladimira LOSTAKOVA (203 Czech Republic), Pavlina MUSILOVA (203 Czech Republic), Hana SULDOVA (203 Czech Republic), Radka MOKOSOVA (203 Czech Republic), Jurij DIDYK (203 Czech Republic), Lenka SISAKOVA (203 Czech Republic), Pavlina LISA (203 Czech Republic), Jaroslav LNENICKA (203 Czech Republic), Hana DARICKOVA (203 Czech Republic), Daniel DOLEZEL (203 Czech Republic), Jana PSIKALOVA (203 Czech Republic), Richard TYL (203 Czech Republic), Renata KRALOVA (203 Czech Republic) and Martina KOZIAR VASAKOVA (203 Czech Republic)
Edition
BMC Pulmonary Medicine, London, BMC, 2023, 1471-2466
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30203 Respiratory systems
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.100 in 2022
RIV identification code
RIV/00216224:14110/23:00131022
Organization unit
Faculty of Medicine
UT WoS
000981017500001
Keywords in English
Idiopathic pulmonary fibrosis; Nintedanib; Lung function decline; Overall survival
Tags
International impact, Reviewed
Změněno: 21/6/2023 09:06, Mgr. Tereza Miškechová
Abstract
V originále
IntroductionThe antifibrotic drug nintedanib is used for the treatment of idiopathic pulmonary fibrosis (IPF). We analysed the effect of nintedanib on antifibrotic treatment outcome in real-world cohorts of Czech EMPIRE registry.Patients/methodsData of 611 Czech IPF subjects, 430 (70%) treated with nintedanib (NIN group), 181 (30%) with no-antifibrotic treatment (NAF group) were analysed. The influence of nintedanib on overall survival (OS), pulmonary function parameters as forced vital capacity (FVC) and diffusing lung capacity for carbon monoxide (DLCO), as well as GAP score (gender, age, physiology) and and CPI (composite physiological index) were investigated.ResultsDuring 2 year follow-up we observed that nintedanib treated patients had longer OS, compared to those treated with no-antifibrotic drugs (p < 0.00001). Nintedanib reduces risk of mortality over no-antifibrotic treatment by 55% (p < 0.001). We have observed no significant difference in the rate of FVC and DLCO decline between the NIN and NAF group. Changes within 24 months from baseline in CPI were not significant between the groups (NAF and NIN).ConclusionOur real-practice study showed the benefit of nintedanib treatment on survival. There were no significant differences between NIN and NAF groups in changes from baseline in FVC %, DLCO % predicted and CPI.