Scientific Reports (May 2021)

Long-term results of sirolimus treatment in lymphangioleiomyomatosis: a single referral centre experience

  • Eva Revilla-López,
  • Cristina Berastegui,
  • Alejandra Méndez,
  • Berta Sáez-Giménez,
  • Victoria Ruiz de Miguel,
  • Manuel López-Meseguer,
  • Victor Monforte,
  • Carlos Bravo,
  • Miguel Angel Pujana,
  • Maria Antonia Ramon,
  • Susana Gómez-Ollés,
  • Antonio Roman,
  • The Vall d’Hebron Multidisciplinary Cystic Lung Disease Group

DOI
https://doi.org/10.1038/s41598-021-89562-0
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 9

Abstract

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Abstract There are few published data on long-term treatment with sirolimus in lymphangioleiomyomatosis (LAM). The objective of this study was to describe the long-term effect of sirolimus in a series of LAM patients followed up in a referral centre, focusing on pulmonary function. We retrospectively reviewed a series of 48 patients with LAM diagnosed, followed up and treated with sirolimus in a single centre. Response to sirolimus was evaluated at 1 and 5 years. A negative sirolimus response was defined as an FEV1 decline greater than − 75 ml/year. A mixed-effects model was used to estimate the longitudinal changes in FEV1 (average slope), both as absolute (ml/year) and as predicted values (%predicted/year). From a total of 48 patients, 9 patients underwent lung transplantation and 4 died during the study. Mean (95% CI) FEV1 slope over 5 years was − 0.14 (− 26.13 to 25.85) ml/year in the whole LAM group, 42.55 (14.87 to 70.22) ml/year in the responder group, − 54.00 (− 71.60 to − 36.39) ml/year in the partial responder group and − 84.19 (− 113.5 to − 54.0) ml/year in the non-responder group. After 5 years of sirolimus treatment 59% had a positive response, 30% had a partial response and 11% had a negative response. Our study found that sirolimus treatment had a positive long-term effect on most LAM patients.