Advanced Imaging Technologies for the Detection of Dysplasia and Early Cancer in Barrett Esophagus.
- Author:
Alberto ESPINO
1
;
Maria CIROCCO
;
Ralph DACOSTA
;
Norman MARCON
Author Information
1. Division of Gastroenterology, Department of Medicine, The Center for Advanced Therapeutic Endoscopy and Endoscopic Oncology, St. Michael's Hospital, University of Toronto Faculty of Medicine, Toronto, ON, Canada. norman.marcon@utoronto.ca
- Publication Type:Review
- Keywords:
Barrett esophagus;
Esophageal adenocarcinoma;
Advanced imaging
- MeSH:
Adenocarcinoma;
Barrett Esophagus*;
Biopsy;
Cost-Benefit Analysis;
Endoscopes;
Endoscopy;
Incidence;
Lymph Nodes;
Neoplasm Metastasis;
Prognosis
- From:Clinical Endoscopy
2014;47(1):47-54
- CountryRepublic of Korea
- Language:English
-
Abstract:
Advanced esophageal adenocarcinomas arising from Barrett esophagus (BE) are tumors with an increasing incidence and poor prognosis. The aim of endoscopic surveillance of BE is to detect dysplasia, particularly high-grade dysplasia and intramucosal cancers that can subsequently be treated endoscopically before progression to invasive cancer with lymph node metastases. Current surveillance practice standards require the collection of random 4-quadrant biopsy specimens over every 1 to 2 cm of BE (Seattle protocol) to detect dysplasia with the assistance of white light endoscopy, in addition to performing targeted biopsies of recognizable lesions. This approach is labor-intensive but should currently be considered state of the art. Chromoendoscopy, virtual chromoendoscopy (e.g., narrow band imaging), and confocal laser endomicroscopy, in addition to high-definition standard endoscopy, might increase the diagnostic yield for the detection of dysplastic lesions. Until these modalities have been demonstrated to enhance efficiency or cost effectiveness, the standard protocol will remain careful examination using conventional off the shelf high-resolution endoscopes, combined with as longer inspection time which is associated with increased detection of dysplasia.
