Evidence map›Paper›PMID 31285305›Full record

ReviewThe European respiratory journal2019

Potential of nintedanib in treatment of progressive fibrosing interstitial lung diseases.

Lutz Wollin, Jörg H W Distler, Elizabeth F Redente, David W H Riches, Susanne Stowasser, Rozsa Schlenker-Herceg, Toby M Maher, Martin Kolb

Open access · hybridAbstract readReview
In one paragraph

Review in The European respiratory journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 145 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
145citing papers in PubMed, 2 pooled it
27.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

145 citing papers in PubMed, 2 syntheses or guidelines pooled it, 293 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Trial
  4. Trial
  5. Biomarkers associated with pulmonary exacerbations in a randomized trial of nintedanib for radiation pneumonitis.Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology · 2024
    Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Trial
  13. Trial
  14. Article
  15. Association ofInternational journal of molecular sciences · 2026
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

85 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 4 countries.

Lutz WollinBoehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany stefan-lutz.wollin@boehringer-ingelheim.com.
Jörg H W DistlerDept of Internal Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander University Erlangen-Nürnberg (FAU) and University Hospital Erlangen, Erlangen, Germany.
Elizabeth F RedenteProgram in Cell Biology, Dept of Pediatrics, National Jewish Health, Denver, CO, USA.
David W H RichesProgram in Cell Biology, Dept of Pediatrics, National Jewish Health, Denver, CO, USA.
Susanne StowasserBoehringer Ingelheim International GmbH, Ingelheim, Germany.
Rozsa Schlenker-HercegBoehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT, USA.
Toby M MaherNational Heart and Lung Institute, Imperial College London, London, UK.
Martin KolbDept of Respiratory Medicine, Pathology and Molecular Medicine, McMaster University and St Joseph's Healthcare, Hamilton, ON, Canada.ORCID 0000-0003-3837-1467
Boehringer Ingelheim (Germany) · DENational Jewish Health · USBoehringer Ingelheim (United States) · USFriedrich-Alexander-Universität Erlangen-Nürnberg · DENational Institute for Health Research · GBSt. Joseph’s Healthcare Hamilton · CA

Funding

Fibroblast Resistance to Apoptosis in Pulmonary FibrosisR01HL140595 · NHLBI · NATIONAL JEWISH HEALTH · PI RICHES, DAVID W. · 2018 to 2021
$2.5M
NHLBI NIH HHS R01 HL140595
6 · The paper itself

Abstract

A proportion of patients with fibrosing interstitial lung diseases (ILDs) develop a progressive phenotype characterised by decline in lung function, worsening quality of life and early mortality. Other than idiopathic pulmonary fibrosis (IPF), there are no approved drugs for fibrosing ILDs and a poor evidence base to support current treatments. Fibrosing ILDs with a progressive phenotype show commonalities in clinical behaviour and in the pathogenic mechanisms that drive disease worsening. Nintedanib is an intracellular inhibitor of tyrosine kinases that has been approved for treatment of IPF and has recently been shown to reduce the rate of lung function decline in patients with ILD associated with systemic sclerosis (SSc-ILD).

Indexed as

AnimalsAnti-Inflammatory AgentsBleomycinDisease Models, AnimalDisease ProgressionExtracellular MatrixFibroblastsFibrosisHumansIdiopathic Pulmonary FibrosisIndolesLungLung Diseases, InterstitialMicePhenotypeProtein Kinase InhibitorsAnti-Inflammatory AgentsBleomycinIndolesnintedanibProtein Kinase Inhibitors

Identifiers

PMID31285305
PMCPMC6751387
OpenAlexW2956457443

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.