Detailed Information on Publication Record
2019
Long-Term Effects and Adverse Events of Nintedanib Therapy in Idiopathic Pulmonary Fibrosis Patients with Functionally Advanced Disease
BARCZI, Eniko, Livia STAROBINSKI, Abigel KOLONICS-FARKAS, Noemi ESZES, Aniko BOHACS et. al.Basic information
Original name
Long-Term Effects and Adverse Events of Nintedanib Therapy in Idiopathic Pulmonary Fibrosis Patients with Functionally Advanced Disease
Authors
BARCZI, Eniko (348 Hungary), Livia STAROBINSKI (348 Hungary), Abigel KOLONICS-FARKAS (348 Hungary), Noemi ESZES (348 Hungary), Aniko BOHACS (348 Hungary), Martina VASAKOVA (203 Czech Republic), Karel HEJDUK (203 Czech Republic, belonging to the institution) and Veronika MULLER (348 Hungary, guarantor)
Edition
ADVANCES IN THERAPY, NEW YORK, SPRINGER, 2019, 0741-238X
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10103 Statistics and probability
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.871
RIV identification code
RIV/00216224:14110/19:00109663
Organization unit
Faculty of Medicine
UT WoS
000466110000021
Keywords in English
IPF; Nintedanib; Pharmacotherapy; Respiratory; pulmonary; Safety; Severe IPF; Survival
Tags
International impact, Reviewed
Změněno: 16/5/2019 12:24, Soňa Böhmová
Abstract
V originále
IntroductionIdiopathic pulmonary fibrosis (IPF) is one of the most common interstitial lung diseases with limited survival. The effect of IPF therapy in patients with severely impaired lung function is not well established. The aim of this study was to characterize IPF patients with a forced vital capacity (FVC)<50% (group 1) and FVC 50-60% predicted (group 2) and analyze the effect and adverse events of nintedanib in Hungarian patients diagnosed between April 2015 and July 2017.MethodsThe impact of nintedanib therapy on lung function, survival, and adverse events was analyzed longitudinally.ResultsTwenty-two out of 103 patients were included in the analysis (group 1: N=10; male/female=6:4, age 62.610.8years and group 2: N=12; male/female=3:9, age 65.7 +/- 11.6years). Eighteen patients were treated with nintedanib (8 in group 1, 10 in group 2); treatment stabilized lung function in 42% and 50%, respectively, in the two groups. Median survival was 444days for group 1 and 476days for group 2. Adverse events were less common than in clinical trials; dose reduction was necessary in three cases, drug discontinuation in two cases. No differences between groups were identified regarding clinical parameters and radiological pattern; however, hypertension as comorbidity was more common in group 1 patients.Conclusions Nintedanib therapy was effective and well tolerated even among patients with severely impaired lung function. Longitudinal follow-up confirmed high mortality in patients with very severe and severe IPF; however, median survival was meaningful as it exceeded 1year in both groups.