Skip to Main content Skip to Navigation
Journal articles

Efficacy and safety of nintedanib in patients with advanced idiopathic pulmonary fibrosis

Abstract : Background - The two 52-week INPULSIS trials investigated nintedanib versus placebo in patients with IPF, FVC ≥50% predicted and DLco 30-79% predicted. The 24-week INSTAGE trial investigated nintedanib plus sildenafil versus nintedanib alone in patients with IPF and DLco ≤35% predicted. We used data from INPULSIS and INSTAGE to compare the effects of nintedanib in patients with IPF with less versus more severe impairment in gas exchange at baseline. Methods - Analyses were conducted in patients treated with nintedanib alone in the INPULSIS and INSTAGE trials and in patients treated with placebo in the INPULSIS trials. Outcomes included the rate of decline in FVC over 24 weeks, the proportions of patients who had a confirmed or suspected idiopathic acute exacerbation over 24 weeks, deaths over 24 weeks, and adverse events. Analyses were descriptive. Results - In total, 638 and 136 patients received nintedanib alone in the INPULSIS and INSTAGE trials, respectively, and 423 patients received placebo in the INPULSIS trials. Rates of FVC decline were - 52.3 and - 66.7 mL/24 weeks in patients treated with nintedanib alone in INPULSIS and INSTAGE, respectively, and - 102.8 mL/24 weeks in patients treated with placebo in INPULSIS. Confirmed or suspected idiopathic acute exacerbations were reported in 0.6 and 3.7% of patients treated with nintedanib alone in INPULSIS and INSTAGE, respectively, and 2.1% of patients treated with placebo in INPULSIS. Deaths occurred in 2.0, 11.0 and 1.9% of patients in these groups, respectively. Diarrhoea adverse events were reported in 52.5 and 48.5% of patients treated with nintedanib alone in INPULSIS and INSTAGE, respectively, and 16.1% of patients treated with placebo in INPULSIS. Conclusions - Based on data from the INSTAGE and INPULSIS trials, nintedanib had a similar effect on FVC decline over 24 weeks, and a similar safety and tolerability profile, in patients with IPF and more versus less severe impairment in gas exchange. These data support the use of nintedanib in patients with IPF who have advanced disease. Trial registration - INPULSIS (NCT01335464 and NCT01335477); INSTAGE (NCT02802345).
Complete list of metadatas

https://hal-univ-rennes1.archives-ouvertes.fr/hal-02470896
Contributor : Laurent Jonchère <>
Submitted on : Friday, July 17, 2020 - 2:47:03 PM
Last modification on : Wednesday, October 14, 2020 - 4:14:57 AM

File

s12890-019-1030-4
Publisher files allowed on an open archive

Identifiers

Citation

Luca Richeldi, Martin Kolb, Stéphane Jouneau, Wim A Wuyts, Birgit Schinzel, et al.. Efficacy and safety of nintedanib in patients with advanced idiopathic pulmonary fibrosis. BMC Pulmonary Medicine, BioMed Central, 2020, 20 (1), pp.3. ⟨10.1186/s12890-019-1030-4⟩. ⟨hal-02470896⟩

Share

Metrics

Record views

74

Files downloads

50