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.Základní údaje
Originální název
Long-Term Effects and Adverse Events of Nintedanib Therapy in Idiopathic Pulmonary Fibrosis Patients with Functionally Advanced Disease
Autoři
BARCZI, Eniko (348 Maďarsko), Livia STAROBINSKI (348 Maďarsko), Abigel KOLONICS-FARKAS (348 Maďarsko), Noemi ESZES (348 Maďarsko), Aniko BOHACS (348 Maďarsko), Martina VASAKOVA (203 Česká republika), Karel HEJDUK (203 Česká republika, domácí) a Veronika MULLER (348 Maďarsko, garant)
Vydání
ADVANCES IN THERAPY, NEW YORK, SPRINGER, 2019, 0741-238X
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10103 Statistics and probability
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.871
Kód RIV
RIV/00216224:14110/19:00109663
Organizační jednotka
Lékařská fakulta
UT WoS
000466110000021
Klíčová slova anglicky
IPF; Nintedanib; Pharmacotherapy; Respiratory; pulmonary; Safety; Severe IPF; Survival
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 16. 5. 2019 12:24, Soňa Böhmová
Anotace
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.