Scientific Reports (Aug 2023)

Nintedanib administration after the onset of acute exacerbation of interstitial lung disease in the real world

  • Motoyasu Kato,
  • Shinichi Sasaki,
  • Wataru Mori,
  • Makiko Kohmaru,
  • Takashi Akimoto,
  • Eri Hayakawa,
  • Soichiro Soma,
  • Yuta Arai,
  • Naho Sakamoto Matsubara,
  • Shun Nakazawa,
  • Takuto Sueyasu,
  • Haruki Hirakawa,
  • Hiroaki Motomura,
  • Issei Sumiyoshi,
  • Yusuke Ochi,
  • Junko Watanabe,
  • Kazuaki Hoshi,
  • Kotaro Kadoya,
  • Hiroaki Ihara,
  • Jia Hou,
  • Shinsaku Togo,
  • Kazuhisa Takahashi

DOI
https://doi.org/10.1038/s41598-023-39101-w
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 9

Abstract

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Abstract Nintedanib reduces the decline in forced vital capacity and extends the time to the first acute exacerbation of interstitial lung disease (AE-ILD). However, the effect of additional nintedanib administration after AE-ILD onset is unknown. This study aimed to investigate the efficacy and safety of nintedanib administration after AE-ILD development. We retrospectively collected the data of 33 patients who developed AE-ILD between April 2014 and January 2022. Eleven patients who received nintedanib after AE-ILD development and the remaining who did not were classified into the N and No-N groups, respectively. The survival time in the N group tended to be longer than that in the No-N group. The generalized Wilcoxson test revealed that the cumulative mortality at 90 days from AE-ILD onset was significantly lower in the N group. The time to subsequent AE-ILD development was significantly longer in the N group than that in the No-N group. The incidence of adverse gastrointestinal effects and liver dysfunction in the N group was 9–18%. Treatment without nintedanib after AE-ILD development and the ratio of arterial oxygen partial pressure to fractional inspired oxygen were significant independent prognostic factors in the multivariate analysis. Thus, nintedanib administration may be a treatment option for AE-ILD.