Anti-fibrotic therapy and lung transplant outcomes in patients with idiopathic pulmonary fibrosis

  • Todd L. Astor
  • , Hilary J. Goldberg
  • , Laurie D. Snyder
  • , Andrew Courtwright
  • , Ramsey Hachem
  • , Tahuanty Pena
  • , Lorenzo Zaffiri
  • , Gerard J. Criner
  • , Marie M. Budev
  • , Tany Thaniyavarn
  • , Thomas B. Leonard
  • , Shaun Bender
  • , Aliaa Barakat
  • , Janis L. Breeze
  • , Peter LaCamera

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Background: It is unclear whether continuing anti-fibrotic therapy until the time of lung transplant increases the risk of complications in patients with idiopathic pulmonary fibrosis. Objectives: To investigate whether the time between discontinuation of anti-fibrotic therapy and lung transplant in patients with idiopathic pulmonary fibrosis affects the risk of complications. Methods: We assessed intra-operative and post-transplant complications among patients with idiopathic pulmonary fibrosis who underwent lung transplant and had been treated with nintedanib or pirfenidone continuously for ⩾ 90 days at listing. Patients were grouped according to whether they had a shorter (⩽ 5 medication half-lives) or longer (> 5 medication half-lives) time between discontinuation of anti-fibrotic medication and transplant. Five half-lives corresponded to 2 days for nintedanib and 1 day for pirfenidone. Results: Among patients taking nintedanib (n = 107) or pirfenidone (n = 190), 211 (71.0%) had discontinued anti-fibrotic therapy ⩽ 5 medication half-lives before transplant. Anastomotic and sternal dehiscence occurred only in this group (anastomotic: 11 patients [5.2%], p = 0.031 vs patients with longer time between discontinuation of anti-fibrotic medication and transplant; sternal: 12 patients [5.7%], p = 0.024). No differences were observed in surgical wound dehiscence, length of hospital stay, or survival to discharge between groups with a shorter versus longer time between discontinuation of anti-fibrotic therapy and transplant. Conclusion: Anastomotic and sternal dehiscence only occurred in patients with idiopathic pulmonary fibrosis who discontinued anti-fibrotic therapy < 5 medication half-lives before transplant. The frequency of other intra-operative and post-transplant complications did not appear to differ depending on when anti-fibrotic therapy was discontinued. Registration: clinicaltrials.gov NCT04316780: https://clinicaltrials.gov/ct2/show/NCT04316780

Original languageEnglish
JournalTherapeutic Advances in Respiratory Disease
Volume17
DOIs
StatePublished - Jan 1 2023

Keywords

  • interstitial lung disease
  • pulmonary fibrosis
  • surgery
  • tyrosine kinase
  • wound healing

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