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

被引:1
作者
Kato, Motoyasu [1 ]
Sasaki, Shinichi [1 ]
Mori, Wataru [1 ]
Kohmaru, Makiko [1 ]
Akimoto, Takashi [1 ]
Hayakawa, Eri [1 ]
Soma, Soichiro [1 ]
Arai, Yuta [1 ]
Matsubara, Naho Sakamoto [1 ]
Nakazawa, Shun [1 ]
Sueyasu, Takuto [1 ]
Hirakawa, Haruki [1 ]
Motomura, Hiroaki [1 ]
Sumiyoshi, Issei [1 ]
Ochi, Yusuke [1 ]
Watanabe, Junko [1 ]
Hoshi, Kazuaki [1 ]
Kadoya, Kotaro [1 ]
Ihara, Hiroaki [1 ]
Hou, Jia [1 ]
Togo, Shinsaku [1 ]
Takahashi, Kazuhisa [1 ]
机构
[1] Juntendo Univ, Grad Sch Med, Dept Resp Med, 3-1-3 Hongo,Bunkyo ku, Tokyo 1138431, Japan
基金
日本学术振兴会;
关键词
IDIOPATHIC PULMONARY-FIBROSIS; TRIPLE ANGIOKINASE INHIBITOR; DOUBLE-BLIND; JAPANESE PATIENTS; BIBF; 1120; SAFETY; EFFICACY; VEGF; BEVACIZUMAB; CARBOPLATIN;
D O I
10.1038/s41598-023-39101-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:9
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