Therapeutic Advances in Respiratory Disease (Apr 2023)

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

DOI
https://doi.org/10.1177/17534666231165912
Journal volume & issue
Vol. 17

Abstract

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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