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Outcome of lung transplantation for adults with interstitial lung disease associated with genetic disorders of the surfactant system.
Bermudez, Julien; Nathan, Nadia; Coiffard, Benjamin; Roux, Antoine; Hirschi, Sandrine; Degot, Tristan; Bunel, Vincent; Le Pavec, Jérôme; Macey, Julie; Le Borgne, Aurélie; Legendre, Marie; Cottin, Vincent; Thomas, Pascal-Alexandre; Borie, Raphaël; Reynaud-Gaubert, Martine.
Afiliación
  • Bermudez J; Department of Respiratory Medicine and Lung Transplantation, Assistance Publique - Hôpitaux de Marseille, Hôpital Nord; Aix-Marseille Université, Marseille, France.
  • Nathan N; Assistance Publique - Hôpitaux de Paris (APHP) - Sorbonne Université, Inserm Childhood Genetic Disorders and Reference Center for Rare Lung Diseases, Armand Trousseau Hospital, Paris, France.
  • Coiffard B; APHP - Sorbonne Université, Pediatric Pulmonology Department and Reference Center for Rare Lung Diseases RespiRare, Armand Trousseau Hospital, Paris, France.
  • Roux A; Department of Respiratory Medicine and Lung Transplantation, Assistance Publique - Hôpitaux de Marseille, Hôpital Nord; Aix-Marseille Université, Marseille, France.
  • Hirschi S; Department of Pulmonary Medicine, Foch Hospital, Suresnes, France.
  • Degot T; Respiratory Medicine and Lung Transplantation, Strasbourg University Hospital, Strasbourg, France.
  • Bunel V; Respiratory Medicine and Lung Transplantation, Strasbourg University Hospital, Strasbourg, France.
  • Le Pavec J; AP-HP, Bichat Claude Bernard Hospital, Pulmonology B and Lung Transplant Department, INSERM 1152, Paris, France.
  • Macey J; Service de Pneumologie et de Transplantation Pulmonaire, Hôpital Marie-Lannelongue, Groupe hospitalier Paris-Saint Joseph, Le Plessis-Robinson, France.
  • Le Borgne A; Université Paris-Sud, Faculté de Médecine, Université Paris-Saclay, Le Kremlin Bicêtre, France.
  • Legendre M; UMR_S 999, Université Paris-Sud, INSERM, Hôpital Marie Lannelongue, Le Plessis Robinson, France.
  • Cottin V; Respiratory Medicine and Cystic Fibrosis Center, University Hospital Center of Bordeaux, Bordeaux, France.
  • Thomas PA; Service de Pneumologie, Pôle des voies respiratoires, Hôpital Larrey, CHU Toulouse, Toulouse, France.
  • Borie R; Assistance Publique - Hôpitaux de Paris (APHP) - Sorbonne Université, Inserm Childhood Genetic Disorders and Reference Center for Rare Lung Diseases, Armand Trousseau Hospital, Paris, France.
  • Reynaud-Gaubert M; UF de Génétique moléculaire, APHP, Sorbonne Université, Hôpital Armand-Trousseau, Paris, France.
ERJ Open Res ; 9(6)2023 Nov.
Article en En | MEDLINE | ID: mdl-38020562
Background: Interstitial lung disease associated with genetic disorders of the surfactant system is a rare entity in adults that can lead to lung transplantation. Our objective was to describe the outcome of these patients after lung transplantation. Methods: We conducted a retrospective, multicentre study, on adults who underwent lung transplantation for such disease in the French lung transplant centres network, from 1997 to 2018. Results: 20 patients carrying mutations in SFTPA1 (n=5), SFTPA2 (n=7) or SFTPC (n=8) were included. Median interquartile range (IQR) age at diagnosis was 45 (40-48) years, and median (IQR) age at lung transplantation was 51 (45-54) years. Median overall survival after transplantation was 8.6 years. Two patients had a pre-transplant history of lung cancer, and two developed post-transplant lung cancer. Female gender and a body mass index <25 kg·m-2 were significantly associated with a better prognosis, whereas transplantation in high emergency was associated with a worst prognosis. Conclusions: Lung transplantation in adults with interstitial lung disease associated with genetic disorders of surfactant system may be a valid therapeutic option. Our data suggest that these patients may have a good prognosis. Immunosuppressive protocol was not changed for these patients, and close lung cancer screening is needed before and after transplantation.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: ERJ Open Res Año: 2023 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: ERJ Open Res Año: 2023 Tipo del documento: Article País de afiliación: Francia