Using chest CT scan and unsupervised machine learning for predicting and evaluating response to lumacaftor-ivacaftor in people with cystic fibrosis.


Journal

The European respiratory journal
ISSN: 1399-3003
Titre abrégé: Eur Respir J
Pays: England
ID NLM: 8803460

Informations de publication

Date de publication:
18 Nov 2021
Historique:
received: 11 05 2021
accepted: 12 10 2021
entrez: 19 11 2021
pubmed: 20 11 2021
medline: 20 11 2021
Statut: aheadofprint

Résumé

Lumacaftor-ivacaftor is a cystic fibrosis transmembrane conductance regulator (CFTR) modulator known to improve clinical status in people with cystic fibrosis (CF). This study aimed to assess lung structural changes after one year of lumacaftor-ivacaftor treatment, and to use unsupervised machine learning to identify morphological phenotypes of lung disease that are associated with response to lumacaftor-ivacaftor. Adolescents and adults with CF from the French multicenter real-world prospective observational study evaluating the first year of treatment with lumacaftor-ivacaftor were included if they had pretherapeutic and follow-up chest computed tomography (CT)-scans available. CT scans were visually scored using a modified Bhalla score. A k-mean clustering method was performed based on 120 radiomics features extracted from unenhanced pretherapeutic chest CT scans. A total of 283 patients were included. The Bhalla score significantly decreased after 1 year of lumacaftor-ivacaftor (-1.40±1.53 points compared with pretherapeutic CT; p<0.001). This finding was related to a significant decrease in mucus plugging (-0.35±0.62 points; p<0.001), bronchial wall thickening (-0.24±0.52 points; p<0.001) and parenchymal consolidations (-0.23±0.51 points; p<0.001). Cluster analysis identified 3 morphological clusters. Patients from cluster C were more likely to experience an increase in percent predicted forced expiratory volume in 1 sec (ppFEV One year treatment with lumacaftor-ivacaftor was associated with a significant visual improvement of bronchial disease on chest CT. Radiomics features on pretherapeutic CT scan may help in predicting lung function response under lumacaftor-ivacaftor.

Identifiants

pubmed: 34795038
pii: 13993003.01344-2021
doi: 10.1183/13993003.01344-2021
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : ErratumIn

Informations de copyright

Copyright ©The authors 2021. For reproduction rights and permissions contact permissions@ersnet.org.

Auteurs

Alienor Campredon (A)

Radiology department, Hôpital Cochin, AP-HP.Centre Université de Paris, Paris, France.
Université de Paris, Paris, France.

Enzo Battistella (E)

OPIS - OPtimisation Imagerie et Santé; Inria Saclay, Palaiseau, France.
MICS - Mathématiques et Informatique pour la Complexité et les Systèmes, Gif-sur-Yvette, France.

Clémence Martin (C)

Université de Paris, Paris, France.
Respiratory Medicine and Cystic Fibrosis National Reference Center; Cochin Hospital; Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.
ERN-Lung CF network.

Isabelle Durieu (I)

ERN-Lung CF network.
Centre de référence Adulte de la Mucoviscidose, Service de médecine interne, Hospices civils de Lyon, Pierre Bénite, France.
Research on Healthcare Performance RESHAPE, INSERM U1290, Université Claude Bernard Lyon 1, Lyon, France.

Laurent Mely (L)

Hôpital Renée Sabran, Cystic Fibrosis Center, Giens, France.

Christophe Marguet (C)

Pediatric Respiratory Disease and Cystic Fibrosis Center, Hospital, UNIROUEN, Inserm EA 2656, Rouen University Hospital, Normandie Univ, Rouen, France.

Chantal Belleguic (C)

Centre de Ressources et de Compétences de la Mucoviscidose Adulte, Centre Hospitalier Universitaire de Rennes, Rennes, France.

Marlène Murris-Espin (M)

Cystic Fibrosis Center, Service de Pneumologie, Pôle des Voies Respiratoires, Hôpital Larrey, CHU de Toulouse, Toulouse, France.

Raphaël Chiron (R)

Cystic Fibrosis Center, Hôpital Arnaud de Villeneuve, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.

Annlyse Fanton (A)

Department of Pulmonary Medicine, Cystic Fibrosis Resource and Competence Centre for Adults, Dijon University Hospital, France.

Stéphanie Bui (S)

Pediatric Respiratory Disease and Cystic Fibrosis Center and CIC 1401, CHU de Bordeaux, Bordeaux, France.

Martine Reynaud-Gaubert (M)

Department of Respiratory Medicine and Lung Transplantation, Aix Marseille Univ, APHM, Hôpital Nord, Marseille, France.

Philippe Reix (P)

UMR 5558 CNRS, Equipe EMET, Université Claude Bernard Lyon 1, Lyon, France.
Cystic Fibrosis Center, Hospices Civils de Lyon, Lyon, France.

Trieu-Nghi Hoang-Thi (TN)

Radiology department, Hôpital Cochin, AP-HP.Centre Université de Paris, Paris, France.

Maria Vakalopoulou (M)

OPIS - OPtimisation Imagerie et Santé; Inria Saclay, Palaiseau, France.
MICS - Mathématiques et Informatique pour la Complexité et les Systèmes, Gif-sur-Yvette, France.

Marie-Pierre Revel (MP)

Radiology department, Hôpital Cochin, AP-HP.Centre Université de Paris, Paris, France.
Université de Paris, Paris, France.

Jennifer Da Silva (J)

Respiratory Medicine and Cystic Fibrosis National Reference Center; Cochin Hospital; Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.
URC-CIC Paris Descartes Necker Cochin, AP-HP, Hôpital Cochin, Paris, France.

Pierre-Régis Burgel (PR)

Université de Paris, Paris, France pierre-regis.burgel@aphp.fr.
Respiratory Medicine and Cystic Fibrosis National Reference Center; Cochin Hospital; Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.
ERN-Lung CF network.

Guillaume Chassagnon (G)

Radiology department, Hôpital Cochin, AP-HP.Centre Université de Paris, Paris, France.
Université de Paris, Paris, France.

Classifications MeSH