4.6 Article

Nintedanib in Asian patients with progressive fibrosing interstitial lung diseases: Results from the INBUILD trial

Journal

RESPIROLOGY
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1111/resp.14452

Keywords

Asian; clinical trials; forced vital capacity; interstitial lung disease; nintedanib; pulmonary fibrosis

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In the INBUILD trial, nintedanib was found to slow down the decline in forced vital capacity in Asian patients with progressive fibrosing ILDs, although some patients experienced gastrointestinal adverse events.
Background and ObjectiveIn the INBUILD trial in patients with progressive fibrosing interstitial lung diseases (ILDs), nintedanib reduced the rate of decline in forced vital capacity (FVC) with an adverse event profile characterized mainly by gastrointestinal events. We analysed the effects of nintedanib in the subset of Asian subjects. MethodsSubjects with fibrosing ILDs other than idiopathic pulmonary fibrosis who had shown progression of ILD at any time within the prior 24 months despite management deemed appropriate in clinical practice were randomized to receive nintedanib or placebo. We analysed the rate of decline in FVC (ml/year) over 52 weeks in all Asian subjects and in Asian subjects with a usual interstitial pneumonia (UIP)-like fibrotic pattern on high-resolution computed tomography (HRCT). ResultsOne hundred sixty-four subjects in the INBUILD trial were of Asian race. The rate of decline in FVC (ml/year) over 52 weeks in this subgroup was -116.8 in the nintedanib group and -207.9 in the placebo group (difference: 91.0 [95% CI: 8.1, 173.9]; nominal p = 0.03). In Asian subjects with a UIP-like fibrotic pattern on HRCT, the rate of decline in FVC (ml/year) over 52 weeks was -130.1 in the nintedanib group and -224.2 in the placebo group (difference: 94.1 [5.5, 182.7]; nominal p = 0.04). Adverse events led to treatment discontinuation in 19.0% of the nintedanib group and 13.8% of the placebo group. ConclusionIn Asian patients with progressive fibrosing ILDs, nintedanib reduced the rate of decline in FVC with adverse events that were manageable for most patients.

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