Cargando…

A narrative review of Barrett’s esophagus in 2020, molecular and clinical update

Barrett’s esophagus (BE) is a condition resulting from an acquired metaplastic epithelial change in the esophagus in response to gastroesophageal reflux. BE is the only known precursor lesion to esophageal adenocarcinoma, and can progress from non-dysplastic BE (NDBE) to low grade dysplasia (LGD) an...

Descripción completa

Detalles Bibliográficos
Autores principales: Dam, Aamir N., Klapman, Jason
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575938/
https://www.ncbi.nlm.nih.gov/pubmed/33145326
http://dx.doi.org/10.21037/atm-20-4406
_version_ 1783597908449296384
author Dam, Aamir N.
Klapman, Jason
author_facet Dam, Aamir N.
Klapman, Jason
author_sort Dam, Aamir N.
collection PubMed
description Barrett’s esophagus (BE) is a condition resulting from an acquired metaplastic epithelial change in the esophagus in response to gastroesophageal reflux. BE is the only known precursor lesion to esophageal adenocarcinoma, and can progress from non-dysplastic BE (NDBE) to low grade dysplasia (LGD) and high grade dysplasia (HGD), and ultimately invasive carcinoma. Although the risk of developing esophageal adenocarcinoma (EAC) in NBDE is less than 0.5% per year, there has been a rising incidence of EAC in Western countries, which continue to drive efforts to optimize screening and surveillance methods. The current gold standard for diagnosis is esophagogastroduodenoscopy (EGD), and there has been significant interest in alternative, minimally invasive methods for screening which would be more readily accessible in the primary care setting. Surveillance endoscopy in 3–5 years is recommended for NDBE given the low progression to EAC. The mainstay of treatment for LGD and HGD is endoscopic eradication therapy (EET). Visible lesions are treated with endoscopic mucosal resection (EMR) or endoscopic submucosal dissection (ESD). Radiofrequency ablation (RFA) is considered first line therapy for flat dysplastic BE and cryotherapy has shown promising results as an alternate form of treatment for of dysplasia. The molecular progression of BE to EAC is a complex process involving multiple pathways involving genetic and epigenetic modifications. Genomic studies have further led to the understanding of the complex molecular landscape that occurs early and late in the disease process. Promising biomarker panels have been investigated to help with the diagnosis of BE as well as aid in the risk stratification of BE during surveillance. In addition, clinical prediction models have been developed to categorize BE patients in low, intermediate, and high risk for progression to HGD and EAC. Further clinical and translational research is needed to help refine markers and techniques in diagnosis, screening, and surveillance.
format Online
Article
Text
id pubmed-7575938
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher AME Publishing Company
record_format MEDLINE/PubMed
spelling pubmed-75759382020-11-02 A narrative review of Barrett’s esophagus in 2020, molecular and clinical update Dam, Aamir N. Klapman, Jason Ann Transl Med Review Articles on Gastroesophageal Cancer 2020 Barrett’s esophagus (BE) is a condition resulting from an acquired metaplastic epithelial change in the esophagus in response to gastroesophageal reflux. BE is the only known precursor lesion to esophageal adenocarcinoma, and can progress from non-dysplastic BE (NDBE) to low grade dysplasia (LGD) and high grade dysplasia (HGD), and ultimately invasive carcinoma. Although the risk of developing esophageal adenocarcinoma (EAC) in NBDE is less than 0.5% per year, there has been a rising incidence of EAC in Western countries, which continue to drive efforts to optimize screening and surveillance methods. The current gold standard for diagnosis is esophagogastroduodenoscopy (EGD), and there has been significant interest in alternative, minimally invasive methods for screening which would be more readily accessible in the primary care setting. Surveillance endoscopy in 3–5 years is recommended for NDBE given the low progression to EAC. The mainstay of treatment for LGD and HGD is endoscopic eradication therapy (EET). Visible lesions are treated with endoscopic mucosal resection (EMR) or endoscopic submucosal dissection (ESD). Radiofrequency ablation (RFA) is considered first line therapy for flat dysplastic BE and cryotherapy has shown promising results as an alternate form of treatment for of dysplasia. The molecular progression of BE to EAC is a complex process involving multiple pathways involving genetic and epigenetic modifications. Genomic studies have further led to the understanding of the complex molecular landscape that occurs early and late in the disease process. Promising biomarker panels have been investigated to help with the diagnosis of BE as well as aid in the risk stratification of BE during surveillance. In addition, clinical prediction models have been developed to categorize BE patients in low, intermediate, and high risk for progression to HGD and EAC. Further clinical and translational research is needed to help refine markers and techniques in diagnosis, screening, and surveillance. AME Publishing Company 2020-09 /pmc/articles/PMC7575938/ /pubmed/33145326 http://dx.doi.org/10.21037/atm-20-4406 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Review Articles on Gastroesophageal Cancer 2020
Dam, Aamir N.
Klapman, Jason
A narrative review of Barrett’s esophagus in 2020, molecular and clinical update
title A narrative review of Barrett’s esophagus in 2020, molecular and clinical update
title_full A narrative review of Barrett’s esophagus in 2020, molecular and clinical update
title_fullStr A narrative review of Barrett’s esophagus in 2020, molecular and clinical update
title_full_unstemmed A narrative review of Barrett’s esophagus in 2020, molecular and clinical update
title_short A narrative review of Barrett’s esophagus in 2020, molecular and clinical update
title_sort narrative review of barrett’s esophagus in 2020, molecular and clinical update
topic Review Articles on Gastroesophageal Cancer 2020
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575938/
https://www.ncbi.nlm.nih.gov/pubmed/33145326
http://dx.doi.org/10.21037/atm-20-4406
work_keys_str_mv AT damaamirn anarrativereviewofbarrettsesophagusin2020molecularandclinicalupdate
AT klapmanjason anarrativereviewofbarrettsesophagusin2020molecularandclinicalupdate
AT damaamirn narrativereviewofbarrettsesophagusin2020molecularandclinicalupdate
AT klapmanjason narrativereviewofbarrettsesophagusin2020molecularandclinicalupdate