Confocal Laser Endomicroscopy as a Guidance Tool for Pleural Biopsies in Malignant Pleural Mesothelioma.


Journal

Chest
ISSN: 1931-3543
Titre abrégé: Chest
Pays: United States
ID NLM: 0231335

Informations de publication

Date de publication:
10 2019
Historique:
received: 09 12 2018
revised: 01 03 2019
accepted: 02 04 2019
pubmed: 11 5 2019
medline: 15 5 2020
entrez: 11 5 2019
Statut: ppublish

Résumé

Pleural biopsies in patients with suspected malignant pleural mesothelioma (MPM) are often inconclusive resulting in repeat diagnostic procedures. Confocal laser endomicroscopy (CLE) enables real-time imaging on a cellular level. We investigated pleural CLE imaging as a biopsy guidance technique to distinguish malignant from benign pleural disease. Prospective, multicenter study in patients with (suspected) MPM based on PET-CT imaging who were scheduled for pleural biopsies. Patients received 2.5 mL fluorescein intravenously preceding the procedure. In vivo through-the-needle CLE imaging of the pleura and ex vivo CLE imaging of the biopsies were correlated with histology. CLE characteristics for various pleural entities were identified, and their interpretability was tested by CLE video scoring by multiple blinded raters. CLE imaging was successfully obtained in 19 of 20 diagnostic pleural biopsy procedures (thoracoscopy: n = 4, surgical excision: n = 3, CT scan: n = 3, ultrasound: n = 9, esophageal ultrasound guided: n = 1) in 15 patients. CLE videos (n = 89) and corresponding pleural biopsies (n = 105) were obtained. No study-related adverse events occurred. Tumor deposits of MPM were distinguished from areas with pleural fibrosis based on CLE imaging and recognized by raters (n = 3) (interobserver agreement, 0.56; 95% CI, 0.49-0.64). CLE imaging was feasible and safe regardless of the biopsy method. Real-time visualization of pleural abnormalities in epithelial and sarcomatoid MPM could be distinguished from pleural fibrosis. Therefore, CLE has potential as a guidance biopsy tool to reduce the current substantial rate of repeat biopsy procedures by identification of areas with malignant cells in vivo (smart needle). ClinicalTrials.gov; No.: NCT02689050; URL: www.clinicaltrials.gov.

Sections du résumé

BACKGROUND
Pleural biopsies in patients with suspected malignant pleural mesothelioma (MPM) are often inconclusive resulting in repeat diagnostic procedures. Confocal laser endomicroscopy (CLE) enables real-time imaging on a cellular level. We investigated pleural CLE imaging as a biopsy guidance technique to distinguish malignant from benign pleural disease.
METHODS
Prospective, multicenter study in patients with (suspected) MPM based on PET-CT imaging who were scheduled for pleural biopsies. Patients received 2.5 mL fluorescein intravenously preceding the procedure. In vivo through-the-needle CLE imaging of the pleura and ex vivo CLE imaging of the biopsies were correlated with histology. CLE characteristics for various pleural entities were identified, and their interpretability was tested by CLE video scoring by multiple blinded raters.
RESULTS
CLE imaging was successfully obtained in 19 of 20 diagnostic pleural biopsy procedures (thoracoscopy: n = 4, surgical excision: n = 3, CT scan: n = 3, ultrasound: n = 9, esophageal ultrasound guided: n = 1) in 15 patients. CLE videos (n = 89) and corresponding pleural biopsies (n = 105) were obtained. No study-related adverse events occurred. Tumor deposits of MPM were distinguished from areas with pleural fibrosis based on CLE imaging and recognized by raters (n = 3) (interobserver agreement, 0.56; 95% CI, 0.49-0.64).
CONCLUSIONS
CLE imaging was feasible and safe regardless of the biopsy method. Real-time visualization of pleural abnormalities in epithelial and sarcomatoid MPM could be distinguished from pleural fibrosis. Therefore, CLE has potential as a guidance biopsy tool to reduce the current substantial rate of repeat biopsy procedures by identification of areas with malignant cells in vivo (smart needle).
TRIAL REGISTRY
ClinicalTrials.gov; No.: NCT02689050; URL: www.clinicaltrials.gov.

Identifiants

pubmed: 31075217
pii: S0012-3692(19)31008-6
doi: 10.1016/j.chest.2019.04.090
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT02689050']

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

754-763

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019. Published by Elsevier Inc.

Auteurs

Lizzy Wijmans (L)

Department of Respiratory Medicine, Amsterdam University Medical Centers, Amsterdam.

Paul Baas (P)

Department of Thoracic Oncology, Netherlands Cancer Institute, Amsterdam.

Thomas E Sieburgh (TE)

Department of Respiratory Medicine, Amsterdam University Medical Centers, Amsterdam.

Daniel M de Bruin (DM)

Department of Biomedical Engineering and Physics, Amsterdam University Medical Centers, Amsterdam.

Petra M Ghuijs (PM)

Department of Pathology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Marc J van de Vijver (MJ)

Department of Pathology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Peter I Bonta (PI)

Department of Respiratory Medicine, Amsterdam University Medical Centers, Amsterdam.

Jouke T Annema (JT)

Department of Respiratory Medicine, Amsterdam University Medical Centers, Amsterdam. Electronic address: j.t.annema@amsterdamumc.nl.

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