Exercise-Induced Oxygen Desaturation and Outcomes After Nintedanib Therapy for Fibrosing Interstitial Lung Disease in Patients Without Dyspnea
<b>Background:</b> The degree of exercise-induced oxygen desaturation and outcomes following antifibrotic drug therapy in asymptomatic patients with fibrosing interstitial lung disease (FILD) remain unclear. <b>Methods:</b> We compared clinical data, incidence of annual FILD progression, overall survival, and tolerability after initiating nintedanib between 58 patients with dyspnea and 18 patients without. Annual FILD progression was defined as >10% decrease in forced vital capacity (FVC), >15% decrease in diffusing capacity of the lungs for carbon monoxide (D<sub>LCO</sub>), developing acute exacerbations, or FILD-related death within 1 year of starting nintedanib. Outcomes between the two groups were adjusted for covariates, including age, gender, FVC, D<sub>LCO</sub>, and diagnosis of idiopathic pulmonary fibrosis, all known prognostic factors for FILD. <b>Results:</b> In 6-min walk test, incidence of decrease to <90% of SpO<sub>2</sub> was significantly lower in non-dyspnea group than in dyspnea group (24% vs. 55%, <i>p</i> = 0.028), but incidence of >4% decreases showed no significant difference (71% vs. 89%, <i>p</i> = 0.11) The incidence of annual progression was significantly lower in non-dyspnea than in dyspnea group (17% vs. 53%, adjusted <i>p</i> = 0.026). The relative change in D<sub>LCO</sub> was significantly slower in non-dyspnea group (adjusted <i>p</i> = 0.036), but FVC was not (adjusted <i>p</i> = 0.067). Overall survival was longer in non-dyspnea group (adjusted <i>p</i> = 0.0089). The discontinuation rate and therapeutic period of nintedanib were not significantly different between the groups. <b>Conclusions:</b> Asymptomatic patients with FILD have severe exercise-induced oxygen desaturation and better outcomes after nintedanib therapy than symptomatic patients. Antifibrotic drug therapy should not be avoided solely because of a lack of symptoms.
Authors
- Yoshiaki Zaizen (ORCID: https://orcid.org/0000-0003-2274-4599)
- Toyoshi Yanagihara (ORCID: https://orcid.org/0000-0002-2212-0631)
- Takashi Nouno
- Tomonori Chikasue (ORCID: https://orcid.org/0000-0001-6519-3446)
- Kiminori Fujimoto (ORCID: https://orcid.org/0000-0001-8681-7588)
- Tomoaki Hoshino (ORCID: https://orcid.org/0000-0002-0459-4913)
- Kazuhiro Tabata (ORCID: https://orcid.org/0000-0002-4524-4813)
- Masaki Tominaga (ORCID: https://orcid.org/0000-0002-6972-1338)
- Akiko Sumi (ORCID: https://orcid.org/0000-0002-4830-4033)
- Shuji Matsuura (ORCID: https://orcid.org/0000-0002-5698-9634)
- Yuuya Nishii
- Masaki Okamoto (ORCID: https://orcid.org/0000-0002-9298-3504)
- Atsushi Kawaguchi (ORCID: https://orcid.org/0000-0002-2209-5835)
- Norikazu Matsuo
Institutions
- Kurume University (JP)
- Kagoshima University (JP)
- National Kyushu Medical Center (JP)
- Fukuoka University Hospital (JP)
Publication Details
- Journal
- Journal of Clinical Medicine
- Published
- 2024-12-23
- DOI
- https://doi.org/10.3390/jcm13247865
- Citations
- 1
- Primary Topic
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Type
- article
- Field-Weighted Citation Impact
- 0.42