Journal Article

Disease trajectories in interstitial lung diseases – data from the EXCITING-ILD registry

Hagmeyer, Lars, Skowasch, Dirk, Höffgen, Marc, Wiederhold, Conrad, Markart, Philipp, Schwarzkopf, Larissa, Stolpe, Christoph, Höger, Philipp, Esselmann, Albert, Hammerl, Peter, Maqhuzu, Phillen, Günther, Andreas, Kabitz, Hans-Joachim, Buschulte, Katharina, Kreuter, Michael, Polke, Markus, Joest, Marcus, Pfeifer, Michael, Somogyi, Vivien, Karpavicius, Rainer, Hellmann, Andreas, Behr, Jürgen, Veitshans, Stefan, Lederer, Christoph

2024

Overview

Background Interstitial lung diseases (ILD) comprise a heterogeneous group of mainly chronic lung diseases with different disease trajectories. Progression (PF-ILD) occurs in up to 50% of patients and is associated with increased mortality. Methods The EXCITING-ILD (Exploring Clinical and Epidemiological Characteristics of Interstitial Lung Diseases) registry was analysed for disease trajectories in different ILD. The course of disease was classified as significant (absolute forced vital capacity FVC decline > 10%) or moderate progression (FVC decline 5–10%), stable disease (FVC decline or increase < 5%) or improvement (FVC increase ≥ 5%) during time in registry. A second definition for PF-ILD included absolute decline in FVC % predicted ≥ 10% within 24 months or ≥ 1 respiratory-related hospitalisation. Risk factors for progression were determined by Cox proportional-hazard models and by logistic regression with forward selection. Kaplan-Meier curves were utilised to estimate survival time and time to progression. Results Within the EXCITING-ILD registry 28.5% of the patients died (n = 171), mainly due to ILD (n = 71, 41.5%). Median survival time from date of diagnosis on was 15.5 years (range 0.1 to 34.4 years). From 601 included patients, progression was detected in 50.6% of the patients (n = 304) with shortest median time to progression in idiopathic NSIP (iNSIP; median 14.6 months) and idiopathic pulmonary fibrosis (IPF; median 18.9 months). Reasons for the determination as PF-ILD were mainly deterioration in lung function (PFT; 57.8%) and respiratory hospitalisations (40.6%). In multivariate analyses reduced baseline FVC together with age were significant predictors for progression (OR = 1.00, p < 0.001). Higher GAP indices were a significant risk factor for a shorter survival time (GAP stage III vs. I HR = 9.06, p < 0.001). A significant shorter survival time was found in IPF compared to sarcoidosis (HR = 0.04, p < 0.001), CTD-ILD (HR = 0.33, p < 0.001), and HP (HR = 0.30, p < 0.001). Patients with at least one reported ILD exacerbation as a reason for hospitalisation had a median survival time of 7.3 years (range 0.1 to 34.4 years) compared to 19.6 years (range 0.3 to 19.6 years) in patients without exacerbations (HR = 0.39, p < 0.001). Conclusion Disease progression is common in all ILD and associated with increased mortality. Most important risk factors for progression are impaired baseline forced vital capacity and higher age, as well as acute exacerbations and respiratory hospitalisations for mortality. Early detection of progression remains challenging, further clinical criteria in addition to PFT might be helpful.

• Publisher: BioMed Central,Nature Publishing Group,BMC
• Subject: Carbon monoxide / Epidemiology / Fibrosis / Hospitalization / Humans / Idiopathic Pulmonary Fibrosis / ILD / IPF / Lung diseases / Lung Diseases, Interstitial - diagnosis / Lung Diseases, Interstitial - epidemiology / Lung Diseases, Interstitial - therapy / Medical prognosis / Medicine / Medicine & Public Health / Mortality / Pneumology/Respiratory System / Pneumonia / Progression / Pulmonary fibrosis / Pulmonary fibrosis: new insights / Registries / Regression analysis / Respiratory function / Risk factors / Sarcoidosis / Survival / Trajectory analysis