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High risk of lung cancer in surfactant-related gene variant carriers.
Brudon, Alexandre; Legendre, Marie; Mageau, Arthur; Bermudez, Julien; Bonniaud, Philippe; Bouvry, Diane; Cadranel, Jacques; Cazes, Aurélie; Crestani, Bruno; Dégot, Tristan; Delestrain, Céline; Diesler, Rémi; Epaud, Ralph; Philippot, Quentin; Théou-Anton, Nathalie; Kannengiesser, Caroline; Ba, Ibrahima; Debray, Marie-Pierre; Fanen, Pascale; Manali, Efrosine; Papiris, Spyros; Nathan, Nadia; Amselem, Serge; Gondouin, Antoine; Guillaumot, Anne; Andréjak, Claire; Jouneau, Stephane; Beltramo, Guillaume; Uzunhan, Yurdagul; Galodé, François; Westeel, Virginie; Mehdaoui, Anas; Hirschi, Sandrine; Leroy, Sylvie; Marchand-Adam, Sylvain; Nunes, Hilario; Picard, Clément; Prévot, Grégoire; Reynaud-Gaubert, Martine; De Vuyst, Paul; Wemeau, Lidwine; Defossez, Gautier; Zalcman, Gérard; Cottin, Vincent; Borie, Raphael.
Affiliation
  • Brudon A; Service d'Oncologie Thoracique, Hôpital Bichat, AP-HP, Institut du Cancer AP-HP Nord, Paris, France.
  • Legendre M; Université Paris Cité, Inserm CIC-EC 1425, Paris, France.
  • Mageau A; A. Brudon and M. Legendre contributed equally to this work.
  • Bermudez J; UF de Génétique Moléculaire, Hôpital Armand Trousseau, AP-HP, Paris, France.
  • Bonniaud P; Sorbonne Université, Inserm UMR-S 933, Maladies Génétiques d'Expression Pédiatrique, Paris, France.
  • Bouvry D; A. Brudon and M. Legendre contributed equally to this work.
  • Cadranel J; Département de Médecine Interne, Hôpital Bichat, AP-HP, Paris, France.
  • Cazes A; Université Paris Cité, Inserm IAME UMR 1137 Team Descid, Paris, France.
  • Crestani B; Service de Pneumologie, Centre de Compétences de Maladies Pulmonaires Rares et de Transplantation Pulmonaire, CHU Nord, AP-HM, Marseille, France.
  • Dégot T; Aix-Marseille Université, Marseille, France.
  • Delestrain C; Department of Respiratory Diseases and Intensive Care, Reference Constitutive Center for Adult Rare Pulmonary Diseases, Dijon-Bourgogne University Hospital, University of Burgundy, Inserm UMR1231, Dijon, France.
  • Diesler R; Département de Pneumologie, Hôpital Avicenne, AP-HP, Bobigny, France.
  • Epaud R; Université Paris 13, Inserm UMR U1272, Bobigny, France.
  • Philippot Q; Service de Pneumologie et Oncologie Thoracique, DMU APPROCHES, Hôpital Tenon, AP-HP, Paris, France.
  • Théou-Anton N; Sorbonne Université, GRC04 Theranoscan, Paris, France.
  • Kannengiesser C; Département d'Anatomie Pathologique, Hôpital Bichat, AP-HP, Paris, France.
  • Ba I; Université Paris Cité, Inserm UMR-S 1152 PHERE, Paris, France.
  • Debray MP; Université Paris Cité, Inserm UMR-S 1152 PHERE, Paris, France.
  • Fanen P; Service de Pneumologie A, Hôpital Bichat, AP-HP, Paris, France.
  • Manali E; Centre de Référence pour les Maladies Respiratoires Rares RespiRare, Centre Hospitalier Intercommunal de Créteil, Créteil, France.
  • Papiris S; Université de Paris Est Créteil, Inserm IMRB, Créteil, France.
  • Nathan N; Service de Pneumologie, Centre National Coordinateur de Référence des Pathologies Pulmonaires Rares, ERN-LUNG, Hôpital Louis Pradel, Hospices Civils de Lyon, Lyon, France.
  • Amselem S; Université Claude Bernard Lyon 1, Lyon, France.
  • Gondouin A; Département de Génétique, Hôpital Bichat, AP-HP, Institut du Cancer AP-HP Nord, Paris, France.
  • Guillaumot A; Centre de Référence pour les Maladies Respiratoires Rares RespiRare, Centre Hospitalier Intercommunal de Créteil, Créteil, France.
  • Andréjak C; Université de Paris Est Créteil, Inserm IMRB, Créteil, France.
  • Jouneau S; Université Paris Cité, Inserm UMR-S 1152 PHERE, Paris, France.
  • Beltramo G; Service de Pneumologie A, Hôpital Bichat, AP-HP, Paris, France.
  • Uzunhan Y; Université Paris Cité, Paris, France.
  • Galodé F; Service de Radiologie, Hôpital Bichat, AP-HP, Paris, France.
  • Westeel V; Département de Génétique, Hôpital Bichat, AP-HP, Institut du Cancer AP-HP Nord, Paris, France.
  • Mehdaoui A; Université Paris Cité, Paris, France.
  • Hirschi S; Département de Génétique, Hôpital Bichat, AP-HP, Institut du Cancer AP-HP Nord, Paris, France.
  • Leroy S; Université Paris Cité, Paris, France.
  • Marchand-Adam S; Université Paris Cité, Paris, France.
  • Nunes H; Service de Radiologie, Hôpital Bichat, AP-HP, Paris, France.
  • Picard C; Université de Paris Est Créteil, Inserm IMRB, Créteil, France.
  • Prévot G; Service de Radiologie, Hôpital Bichat, AP-HP, Paris, France.
  • Reynaud-Gaubert M; Département de Pneumologie Pédiatrique, Centre de Référence des Maladies Respiratoires Rares RespiRare, Paris, France.
  • De Vuyst P; General University Hospital "Attikon", Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Wemeau L; Sorbonne Université, Inserm UMR-S 933, Maladies Génétiques d'Expression Pédiatrique, Paris, France.
  • Defossez G; Service de Pneumologie, Centre des Maladies Pulmonaires Rares, Hôpital de Besançon, Besançon, France.
  • Zalcman G; UF de Génétique Moléculaire, Hôpital Armand Trousseau, AP-HP, Paris, France.
  • Cottin V; Sorbonne Université, Inserm UMR-S 933, Maladies Génétiques d'Expression Pédiatrique, Paris, France.
  • Borie R; Service de Pneumologie, Hôpital de Brabois, Vandoeuvre-les-Nancy, France.
Eur Respir J ; 63(5)2024 May.
Article in En | MEDLINE | ID: mdl-38575158
ABSTRACT

BACKGROUND:

Several rare surfactant-related gene (SRG) variants associated with interstitial lung disease are suspected to be associated with lung cancer, but data are missing. We aimed to study the epidemiology and phenotype of lung cancer in an international cohort of SRG variant carriers.

METHODS:

We conducted a cross-sectional study of all adults with SRG variants in the OrphaLung network and compared lung cancer risk with telomere-related gene (TRG) variant carriers.

RESULTS:

We identified 99 SRG adult variant carriers (SFTPA1 (n=18), SFTPA2 (n=31), SFTPC (n=24), ABCA3 (n=14) and NKX2-1 (n=12)), including 20 (20.2%) with lung cancer (SFTPA1 (n=7), SFTPA2 (n=8), SFTPC (n=3), NKX2-1 (n=2) and ABCA3 (n=0)). Among SRG variant carriers, the odds of lung cancer was associated with age (OR 1.04, 95% CI 1.01-1.08), smoking (OR 20.7, 95% CI 6.60-76.2) and SFTPA1/SFTPA2 variants (OR 3.97, 95% CI 1.39-13.2). Adenocarcinoma was the only histological type reported, with programmed death ligand-1 expression ≥1% in tumour cells in three samples. Cancer staging was localised (I/II) in eight (40%) individuals, locally advanced (III) in two (10%) and metastatic (IV) in 10 (50%). We found no somatic variant eligible for targeted therapy. Seven cancers were surgically removed, 10 received systemic therapy, and three received the best supportive care according to their stage and performance status. The median overall survival was 24 months, with stage I/II cancers showing better survival. We identified 233 TRG variant carriers. The comparative risk (subdistribution hazard ratio) for lung cancer in SRG patients versus TRG patients was 18.1 (95% CI 7.1-44.7).

CONCLUSIONS:

The high risk of lung cancer among SRG variant carriers suggests specific screening and diagnostic and therapeutic challenges. The benefit of regular computed tomography scan follow-up should be evaluated.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Pulmonary Surfactant-Associated Protein A / Pulmonary Surfactant-Associated Protein C / Lung Neoplasms Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Pulmonary Surfactant-Associated Protein A / Pulmonary Surfactant-Associated Protein C / Lung Neoplasms Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Year: 2024 Type: Article