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Antithrombin III as predictive indicator of survival in idiopathic pulmonary fibrosis (IPF) patients treated with nintedanib: a preliminary study.

Laura BergantiniMiriana d'AlessandroPaolo CameliAlfonso CarleoClaudia LandiLucia VietriNicola LanzaroneMaria PieroniPiersante SestiniElena Bargagli
Published in: Internal medicine journal (2021)
After 12 months of antifibrotic treatment, IPF patients with high serum ATIII concentrations and high BAL neutrophil percentages had a poor prognosis and increased survival risk. The results of this preliminary study suggest that ATIII has potential as a biomarker of IPF severity and in predicting response to nintedanib therapy. As a marker, ATIII showed several advantages over BAL neutrophil percentage.
Keyphrases
  • idiopathic pulmonary fibrosis
  • poor prognosis
  • long non coding rna
  • interstitial lung disease
  • free survival
  • stem cells
  • mesenchymal stem cells
  • combination therapy
  • replacement therapy