Endoscopic follow-up of low-grade precancerous bronchial lesions in high-risk patients: long-term results of the SELEPREBB randomised multicentre trial.


Journal

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

Informations de publication

Date de publication:
09 2022
Historique:
received: 11 07 2021
accepted: 15 01 2022
pubmed: 4 3 2022
medline: 20 9 2022
entrez: 3 3 2022
Statut: epublish

Résumé

3-9% of low-grade preinvasive bronchial lesions progress to cancer. This study assessed the usefulness of an intensive bronchoscopy surveillance strategy in patients with bronchial lesions up to moderate squamous dysplasia. SELEPREBB (ClinicalTrials.gov NCT00213603) was a randomised study conducted in 17 French centres. After baseline lung computed tomography (CT) and autofluorescence bronchoscopy (AFB) to exclude lung cancer and bronchial severe squamous dysplasia or carcinoma 364 patients were randomised (A: 180, B: 184). 27 patients developed invasive lung cancer and two developed persistent CIS during the study, with no difference between arms (OR 0.63, 95% CI 0.20-1.96, p=0.42). Mild or moderate dysplasia at baseline bronchoscopy was a significant lung cancer risk factor both at 3 years (8 of 74 patients, OR 6.9, 95% CI 2.5-18.9, p<0.001) and at maximum follow-up (16 of 74 patients, OR 5.9, 95% CI 2.9-12.0, p<0.001). Smoking cessation was significantly associated with clearance of bronchial dysplasia on follow-up (OR 0.12, 95% CI 0.01-0.66, p=0.005) and with a reduced risk of lung cancer at 5 years (OR 0.15, 95% CI 0.003-0.99, p=0.04). Patients with mild or moderate dysplasia are at very high risk for lung cancer at 5 years, with smoking cessation significantly reducing the risk. Whereas intensive bronchoscopy surveillance does not improve patient outcomes, the identification of bronchial dysplasia using initial bronchoscopy maybe useful for risk stratification strategies in lung cancer screening programmes.

Sections du résumé

BACKGROUND
3-9% of low-grade preinvasive bronchial lesions progress to cancer. This study assessed the usefulness of an intensive bronchoscopy surveillance strategy in patients with bronchial lesions up to moderate squamous dysplasia.
METHODS
SELEPREBB (ClinicalTrials.gov NCT00213603) was a randomised study conducted in 17 French centres. After baseline lung computed tomography (CT) and autofluorescence bronchoscopy (AFB) to exclude lung cancer and bronchial severe squamous dysplasia or carcinoma
RESULTS
364 patients were randomised (A: 180, B: 184). 27 patients developed invasive lung cancer and two developed persistent CIS during the study, with no difference between arms (OR 0.63, 95% CI 0.20-1.96, p=0.42). Mild or moderate dysplasia at baseline bronchoscopy was a significant lung cancer risk factor both at 3 years (8 of 74 patients, OR 6.9, 95% CI 2.5-18.9, p<0.001) and at maximum follow-up (16 of 74 patients, OR 5.9, 95% CI 2.9-12.0, p<0.001). Smoking cessation was significantly associated with clearance of bronchial dysplasia on follow-up (OR 0.12, 95% CI 0.01-0.66, p=0.005) and with a reduced risk of lung cancer at 5 years (OR 0.15, 95% CI 0.003-0.99, p=0.04).
CONCLUSION
Patients with mild or moderate dysplasia are at very high risk for lung cancer at 5 years, with smoking cessation significantly reducing the risk. Whereas intensive bronchoscopy surveillance does not improve patient outcomes, the identification of bronchial dysplasia using initial bronchoscopy maybe useful for risk stratification strategies in lung cancer screening programmes.

Identifiants

pubmed: 35236723
pii: 13993003.01946-2021
doi: 10.1183/13993003.01946-2021
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT00213603']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright ©The authors 2022. For reproduction rights and permissions contact permissions@ersnet.org.

Déclaration de conflit d'intérêts

Conflict of interest: All authors report payment for study completion to participating institutions from the French Ministry of Health (PHRC National). In addition, within the 36 months prior to manuscript submission: S. Lachkar reports consulting fees and payment or honoraria from Olympus, Fuji and TSC; payment or honoraria from Merck Sharp & Dohme; and participation on a data safety monitoring or advisory board for Boston Scientific. P. Hofman reports consulting fees, payment or honoraria and participation on data safety or advisory boards from AstraZeneca, Bristol Myers Squibb, Merck Sharp & Dohme, Roche, Pfizer, Bayer, Novartis, Illumina, Thermo Fisher, AbbVie, Biocartis and Lilly. G. Zalcman reports consulting fees from Bristol Myers Squibb and AstraZeneca, paid to their institution, and support for attending meetings or travel from AstraZeneca (ASCO 2019), Bristol Myers Squibb (ESMO 2018 and 2019) and AbbVie (ASCO 2019). All other authors declare no additional competing interests.

Auteurs

Florian Guisier (F)

Dept of Pneumology, Normandie Univ, UNIROUEN, LITIS Lab QuantIF team EA4108, CHU Rouen and Inserm CIC-CRB 1404, Rouen, France florian.guisier@chu-rouen.fr.

Gaëtan Deslee (G)

Dept of Pneumology, CHU de Reims, Inserm UMR 1250, Université de Reims-Champagne Ardenne, Reims, France.

Philippe Birembaut (P)

Laboratoire de Pathologie, CHU de Reims, Reims, France.

Bruno Escarguel (B)

Dept of Pneumology, Hôpital Saint-Joseph, Marseille, France.

Françoise Chapel (F)

Laboratoire d'Anatomie Pathologique, CHI Toulon La Seyne sur Mer, Toulon, France.

Suzanna Bota (S)

Dept of Pneumology, CHU de Rouen, Rouen, France.

Josette Métayer (J)

Dept of Pathology, CHU de Rouen, Rouen, France.

Samy Lachkar (S)

Dept of Pneumology, CHU de Rouen, Rouen, France.

Frédérique Capron (F)

Dept of Pathology, Hôpital Pitié Salepetrière, Paris, France.

Jean Paul Homasson (JP)

Dept of Pneumology, Hôpital Chevilly Larue, Chevilly Larue, France.

Marc Taulelle (M)

Hopital Privé Les Franciscaines, Nîmes, France.

Marie Quintana (M)

Centre Médical de Pathologie, Nîmes, France.

Christophe Raspaud (C)

Clinique Pasteur, Toulouse, France.

Daniel Messelet (D)

Laboratoire d'Anatomie et Cytologie Pathologiques, Toulouse, France.

Jonathan Benzaquen (J)

Dept of Pulmonary Medicine and Oncology, Université Côte d'Azur, Centre Hospitalier Universitaire de Nice, FHU OncoAge, Nice, France.
Institute of Research on Cancer and Aging (IRCAN), Université Côte d'Azur, FHU OncoAge, CNRS UMR7284, INSERM U1081, Nice, France.

Paul Hofman (P)

Institute of Research on Cancer and Aging (IRCAN), Université Côte d'Azur, CNRS, INSERM, Nice, France.
Laboratory of Clinical and Experimental Pathology, Université Côte d'Azur, FHU OncoAge, BB-0033-00025, Centre Hospitalier Universitaire de Nice, Nice, France.

Jamal Baddredine (J)

Laboratoire Ouest Pathologie, Rennes, France.

Christophe Paris (C)

INSERM U1085 IRSET and Service de Santé au Travail et de Pathologie Professionnelle et Environnementale, CHRU Pontchaillou, Rennes, France.

Valérie Cales (V)

Laboratoire d'Anatomie Pathologique, CH de Pau, Pau, France.

Philippe Laurent (P)

Service de Pneumologie, CH François Mitterand, Pau, France.

Jean-Michel Vignaud (JM)

Hôpital Central, Laboratoire d'Anatomie Pathologique, Nancy, France.

Olivier Ménard (O)

Service de Pneumologie, CHU Nancy, Hôpital Brabois, Vandoeuvre les Nancy, France.

Marie-Christine Copin (MC)

Institut de Pathologie, Université de Lille, CHRU Lille, Lille, France.

Philippe Ramon (P)

Clinique des Maladies Respiratoires, CHRU Lille, Hôpital Calmette, Lille, France.

Brigitte Bouchindhomme (B)

Laboratoire d'Anatomie Pathologique, CH Lens, Lens, France.

Jean-Yves Tavernier (JY)

Service de Pneumologie, CH Lens, Lens, France.

Isabelle Quintin (I)

Service d'Anatomie Pathologique, CHU Brest, Hôpital Morvan, Brest, France.

Jean-Jacques Quiot (JJ)

Service de Pneumologie, CHU Brest, Hôpital Morvan, Brest, France.

Françoise Galateau-Sallé (F)

Laboratoire d'Anatomie Pathologique, CHU de Caen, Caen, France.
Dept of BioPathology Centre Leon Berard, Lyon, France.

Gérard Zalcman (G)

Service de Pneumologie, CHU de Caen, Caen, France.
Thoracic Oncology Dept, Université de Paris, Hôpital Bichat Claude Bernard, Paris, France.

Nicolas Piton (N)

Service de Pathologie, Normandie Université, UNIROUEN, Inserm U1245, CHU Rouen, Rouen, France.

Luc Thiberville (L)

Dept of Pneumology, Normandie Univ, UNIROUEN, LITIS Lab QuantIF team EA4108, CHU Rouen and Inserm CIC-CRB 1404, Rouen, France.

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