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The effect of nintedanib on lung functions and survival in idiopathic pulmonary fibrosis: real-life analysis of the Czech EMPIRE registry

M. Štefániková, M. Doubková, P. Ovesná, M. Šterclová, L. Lacina, M. Žurková, M. Plačková, V. Bartoš, I. Janíčková, R. Bittenglová, J. Anton, Ľ. Sýkorová, V. Lošťáková, P. Musilová, H. Šuldová, R. Mokošová, J. Didyk, L. Šišáková, P. Lisá, J....

. 2023 ; 23 (1) : 154. [pub] 20230503

Language English Country England, Great Britain

Document type Journal Article

INTRODUCTION: The 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/METHODS: Data 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. RESULTS: During 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). CONCLUSION: Our 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.

Department of Pulmonary Diseases and Tuberculosis Faculty of Medicine and Dentistry Palacky University in Olomouc University Hospital Olomouc Olomouc Czech Republic

Department of Pulmonary diseases and tuberculosis Faculty of Medicine Masaryk University University Hospital Brno Czech Republic

Department of Pulmonary Diseases and Tuberculosis Faculty of Medicine University of Ostrava University Hospital Ostrava Ostrava Czech Republic

Department of Pulmonary Diseases and Tuberculosis Regional Medical Association JSC Masaryk Hospital in Usti nad Labem Usti nad Labem Czech Republic

Department of Pulmonary Medicine and Allergology Hospital Kromeriz Kromeriz Czech Republic

Department of Pulmonary Medicine and Thoracic Surgery Hospital Na Bulovce Prague Czech Republic

Department of Pulmonary Medicine Faculty of Medicine at Charles University Prague University Hospital in Motol Prague Czech Republic

Department of Pulmonary Medicine Faculty of Medicine in Hradec Kralove at Charles University Prague University Hospital Hradec Kralove Hradec Kralove Czech Republic

Department of Pulmonary Medicine Hospital Ceske Budejovice Ceske Budejovice Czech Republic

Department of Pulmonary Medicine Hospital Jihlava Jihlava Czech Republic

Department of Pulmonary Medicine Hospital Novy Jicin Novy Jicin Czech Republic

Department of Pulmonary Medicine Regional Hospital Pardubice Pardubice Czech Republic

Department of Pulmonary Medicine Tomas Bata Regional Hospital Zlin Czech Republic

Department of Pulmonary Medicine University Hospital Plzen Pilsen Czech Republic

Department of Respiratory Medicine University Thomayer Hospital Charles University Prague Czech Republic

Institute of Biostatistics and Analyses Faculty of Medicine Masaryk University Brno Czech Republic

References provided by Crossref.org

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$a INTRODUCTION: The antifibrotic drug nintedanib is used for the treatment of idiopathic pulmonary fibrosis (IPF). We analysed the effect of nintedanib on antifibrotic treatment outcome in real-world cohorts of Czech EMPIRE registry. PATIENTS/METHODS: Data of 611 Czech IPF subjects, 430 (70%) treated with nintedanib (NIN group), 181 (30%) with no-antifibrotic treatment (NAF group) were analysed. The influence of nintedanib on overall survival (OS), pulmonary function parameters as forced vital capacity (FVC) and diffusing lung capacity for carbon monoxide (DLCO), as well as GAP score (gender, age, physiology) and and CPI (composite physiological index) were investigated. RESULTS: During 2 year follow-up we observed that nintedanib treated patients had longer OS, compared to those treated with no-antifibrotic drugs (p < 0.00001). Nintedanib reduces risk of mortality over no-antifibrotic treatment by 55% (p < 0.001). We have observed no significant difference in the rate of FVC and DLCO decline between the NIN and NAF group. Changes within 24 months from baseline in CPI were not significant between the groups (NAF and NIN). CONCLUSION: Our real-practice study showed the benefit of nintedanib treatment on survival. There were no significant differences between NIN and NAF groups in changes from baseline in FVC %, DLCO % predicted and CPI.
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$a Doubková, Martina $u Department of Pulmonary diseases and tuberculosis, Faculty of Medicine, Masaryk University, University Hospital, Brno, Czech Republic
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$a Lacina, Ladislav $u Department of Pulmonary Medicine and Thoracic Surgery, Hospital Na Bulovce, Prague, Czech Republic
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$a Sýkorová, Ľubica $u Department of Pulmonary diseases and tuberculosis, Faculty of Medicine, Masaryk University, University Hospital, Brno, Czech Republic
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$a Musilová, Pavlína $u Department of Pulmonary Medicine, Hospital Jihlava, Jihlava, Czech Republic
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$a Mokošová, Radka $u Department of Pulmonary Diseases and Tuberculosis, Faculty of Medicine, University of Ostrava, University Hospital Ostrava, Ostrava, Czech Republic $7 xx0310631
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