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Survival and course of lung function in the presence or absence of antifibrotic treatment in patients with idiopathic pulmonary fibrosis: long-term results of the INSIGHTS-IPF registry.
Behr, Jürgen; Prasse, Antje; Wirtz, Hubert; Koschel, Dirk; Pittrow, David; Held, Matthias; Klotsche, Jens; Andreas, Stefan; Claussen, Martin; Grohé, Christian; Wilkens, Henrike; Hagmeyer, Lars; Skowasch, Dirk; Meyer, Joachim F; Kirschner, Joachim; Gläser, Sven; Kahn, Nicolas; Welte, Tobias; Neurohr, Claus; Schwaiblmair, Martin; Bahmer, Thomas; Oqueka, Tim; Frankenberger, Marion; Kreuter, Michael.
Afiliação
  • Behr J; Medizinische Klinik und Poliklinik V, LMU Klinikum, University of Munich, Munich, Germany juergen.behr@med.uni-muenchen.de.
  • Prasse A; Comprehensive Pneumology Center (CPC), Lungenforschungsambulanz, LMU Klinikum und Helmholtz Zentrum, Munich, Germany.
  • Wirtz H; Asklepios Fachkliniken, München-Gauting, Germany.
  • Koschel D; German Center for Lung Research (DZL), Germany.
  • Pittrow D; German Center for Lung Research (DZL), Germany.
  • Held M; Klinik für Pneumologie, Medizinische Hochschule Hannover, Hannover, Germany.
  • Klotsche J; Fraunhofer Institute ITEM, Hannover, Germany.
  • Andreas S; Abteilung für Pneumologie, Department Innere Medizin, Neurologie und Dermatologie, Universitätsklinikum Leipzig AöR, Leipzig, Germany.
  • Claussen M; Zentrum für Pneumologie, Fachkrankenhaus Coswig, Coswig, Germany.
  • Grohé C; Institut für Klinische Pharmakologie, Medizinische Fakultät, Technische Universität Dresden, Dresden, Germany.
  • Wilkens H; GWT-TUD GmbH, Pharmacoepidemiology, Dresden, Germany.
  • Hagmeyer L; Department of Internal Medicine, Respiratory Medicine and Ventilatory Support, Medical Mission Hospital, Central Clinic, Würzburg, Germany.
  • Skowasch D; Epidemiologie, Deutsches Rheuma-Forschungszentrum, Berlin, Germany.
  • Meyer JF; Lungenfachklinik Immenhausen und Universitätsmedizin Göttingen, Kardiologie und Pneumologie, Göttingen, Germany.
  • Kirschner J; German Center for Lung Research (DZL), Germany.
  • Gläser S; LungenClinic Grosshansdorf, Großhansdorf, Germany.
  • Kahn N; Klinik für Pneumologie - ELK, Berlin Buch, Berlin, Germany.
  • Welte T; Klinik für Innere Medizin V, Pneumologie, Universitätsklinikum, Universitätskliniken des Saarlandes, Homburg, Germany.
  • Neurohr C; Krankenhaus Bethanien, Klinik für Pneumologie und Allergologie, Zentrum für Schlaf- und Beatmungsmedizin; Institut für Pneumologie, Universität zu Köln, Solingen, Germany.
  • Schwaiblmair M; Medizinische Klinik und Poliklinik II, Universitätsklinikum, Bonn, Germany.
  • Bahmer T; Lungenzentrum München, LZM Bogenhausen-Harlaching, Städtisches Klinikum München GmbH, Munich, Germany.
  • Oqueka T; Center for Internal Medical Studies CIMS, Bamberg, Germany.
  • Frankenberger M; Klinik und Poliklinik für Innere Medizin B, Forschungsbereich Pneumologie und Pneumologische Epidemiologie, Universitätsmedizin Greifswald, Greifswald, Germany.
  • Kreuter M; Klinik für Innere Medizin - Pneumologie und Infektiologie, Vivantes Klinikum Neukölln und Spandau, Berlin, Germany.
Eur Respir J ; 56(2)2020 08.
Article em En | MEDLINE | ID: mdl-32381492
ABSTRACT

OBJECTIVE:

There is a paucity of observational data on antifibrotic therapy for idiopathic pulmonary fibrosis (IPF). We aimed to assess the course of disease of IPF patients with and without antifibrotic therapy under real-life conditions.

METHODS:

We analysed data from a non-interventional, prospective cohort study of consecutively enrolled IPF patients from 20 interstitial lung disease expert centres in Germany. Data quality was ensured by automated plausibility checks, on-site monitoring, and source data verification. Propensity scores were applied to account for known differences in baseline characteristics between patients with and without antifibrotic therapy.

RESULTS:

Among the 588 patients suitable for analysis, the mean±sd age was 69.8±9.1 years, and 81.0% were male. The mean±sd duration of disease since diagnosis was 1.8±3.4 years. The mean±sd value at baseline for forced vital capacity (FVC) and diffusion capacity (D LCO) were 68.6±18.8% predicted and 37.8±18.5% predicted, respectively. During a mean±sd follow-up of 1.2±0.7 years, 194 (33.0%) patients died. The 1-year and 2-year survival rates were 87% versus 46% and 62% versus 21%, respectively, for patients with versus without antifibrotic therapy. The risk of death was 37% lower in patients with antifibrotic therapy (hazard ratio 0.63, 95% CI 0.45; 0.87; p=0.005). The results were robust (and remained statistically significant) on multivariable analysis. Overall decline of FVC and D LCO was slow and did not differ significantly between patients with or without antifibrotic therapy.

CONCLUSIONS:

Survival was significantly higher in IPF patients with antifibrotic therapy, but the course of lung function parameters was similar in patients with and without antifibrotic therapy. This suggests that in clinical practice, premature mortality of IPF patients eventually occurs despite stable measurements for FVC and D LCO.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrose Pulmonar Idiopática Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrose Pulmonar Idiopática Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article