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Artificial intelligence-driven volumetric CT outcome score in cystic fibrosis: longitudinal and multicenter validation with/without modulators treatment.
Hadj Bouzid, Amel Imene; Bui, Stephanie; Benlala, Ilyes; Berger, Patrick; Hutt, Antoine; Liberge, Renan; Habert, Paul; Gaubert, Jean-Yves; Baque-Juston, Marie; Morel, Baptiste; Ferretti, Gilbert; Denis de Senneville, Baudouin; Laurent, François; Macey, Julie; Dournes, Gaël.
  • Hadj Bouzid AI; Univ. Bordeaux, INSERM, Centre de Recherche Cardio-Thoracique de Bordeaux, U1045, CIC 1401, F-33600, Pessac, France.
  • Bui S; Univ. Bordeaux, INSERM, Centre de Recherche Cardio-Thoracique de Bordeaux, U1045, CIC 1401, F-33600, Pessac, France.
  • Benlala I; CHU Bordeaux, Service d'Imagerie Thoracique et Cardiovasculaire, Service des Maladies Respiratoires, Service d'Exploration Fonctionnelle Respiratoire, Paediatric Cystic Fibrosis Reference Center (CRCM), CIC 1401, F-33600, Pessac, France.
  • Berger P; INSERM, U1045, Centre de Recherche Cardio-Thoracique de Bordeaux, CIC 1401, F-33600, Pessac, France.
  • Hutt A; Univ. Bordeaux, INSERM, Centre de Recherche Cardio-Thoracique de Bordeaux, U1045, CIC 1401, F-33600, Pessac, France.
  • Liberge R; CHU Bordeaux, Service d'Imagerie Thoracique et Cardiovasculaire, Service des Maladies Respiratoires, Service d'Exploration Fonctionnelle Respiratoire, Paediatric Cystic Fibrosis Reference Center (CRCM), CIC 1401, F-33600, Pessac, France.
  • Habert P; INSERM, U1045, Centre de Recherche Cardio-Thoracique de Bordeaux, CIC 1401, F-33600, Pessac, France.
  • Gaubert JY; Univ. Bordeaux, INSERM, Centre de Recherche Cardio-Thoracique de Bordeaux, U1045, CIC 1401, F-33600, Pessac, France.
  • Baque-Juston M; CHU Bordeaux, Service d'Imagerie Thoracique et Cardiovasculaire, Service des Maladies Respiratoires, Service d'Exploration Fonctionnelle Respiratoire, Paediatric Cystic Fibrosis Reference Center (CRCM), CIC 1401, F-33600, Pessac, France.
  • Morel B; INSERM, U1045, Centre de Recherche Cardio-Thoracique de Bordeaux, CIC 1401, F-33600, Pessac, France.
  • Ferretti G; Department of Thoracic Imaging, Heart & Lung Institute, Lille, Cedex, France.
  • Denis de Senneville B; Department of Radiology, CHU Nantes, F-44000, Nantes, France.
  • Laurent F; Imaging Department, Hopital La Timone, APHM, Aix Marseille University, Marseille, France.
  • Macey J; Imaging Department, Hopital La Timone, APHM, Aix Marseille University, Marseille, France.
  • Dournes G; Paediatric Radiology Department, Hôpitaux Pédiatriques de Nice CHU-Lenval, Nice, France.
Eur Radiol ; 2024 Aug 16.
Article en En | MEDLINE | ID: mdl-39150489
ABSTRACT

OBJECTIVES:

Holistic segmentation of CT structural alterations with 3D deep learning has recently been described in cystic fibrosis (CF), allowing the measurement of normalized volumes of airway abnormalities (NOVAA-CT) as an automated quantitative outcome. Clinical validations are needed, including longitudinal and multicenter evaluations. MATERIALS AND

METHODS:

The validation study was retrospective between 2010 and 2023. CF patients undergoing Elexacaftor/Tezacaftor/Ivacaftor (ETI) or corticosteroids for allergic broncho-pulmonary aspergillosis (ABPA) composed the monocenter ETI and ABPA groups, respectively. Patients from six geographically distinct institutions composed a multicenter external group. All patients had completed CT and pulmonary function test (PFT), with a second assessment at 1 year in case of ETI or ABPA treatment. NOVAA-CT quantified bronchiectasis, peribronchial thickening, bronchial mucus, bronchiolar mucus, collapse/consolidation, and their overall total abnormal volume (TAV). Two observers evaluated the visual Bhalla score.

RESULTS:

A total of 139 CF patients (median age, 15 years [interquartile range 13-25]) were evaluated. All correlations between NOVAA-CT to both PFT and Bhalla score were significant in the ETI (n = 60), ABPA (n = 20), and External groups (n = 59), such as the normalized TAV (ρ ≥ 0.76; p < 0.001). In both ETI and ABPA groups, there were significant longitudinal improvements in peribronchial thickening, bronchial mucus, bronchiolar mucus and collapse/consolidation (p ≤ 0.001). An additional reversibility in bronchiectasis volume was quantified with ETI (p < 0.001). Intraclass correlation coefficient of reproducibility was > 0.99.

CONCLUSION:

NOVAA-CT automated scoring demonstrates validity, reliability and responsiveness for monitoring CF severity over an entire lung and quantifies therapeutic effects on lung structure at CT, such as the volumetric reversibility of airway abnormalities with ETI. CLINICAL RELEVANCE STATEMENT Normalized volume of airway abnormalities at CT automated 3D outcome enables objective, reproducible, and holistic monitoring of cystic fibrosis severity over an entire lung for management and endpoints during therapeutic trials. KEY POINTS Visual scoring methods lack sensitivity and reproducibility to assess longitudinal bronchial changes in cystic fibrosis (CF). AI-driven volumetric CT scoring correlates longitudinally to disease severity and reliably improves with Elexacaftor/Tezacaftor/Ivacaftor or corticosteroid treatments. AI-driven volumetric CT scoring enables reproducible monitoring of lung disease severity in CF and quantifies longitudinal structural therapeutic effects.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article