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Practice Guideline
. 2024 Jun;166(6):1020-1055.
doi: 10.1053/j.gastro.2024.03.019.

AGA Clinical Practice Guideline on Endoscopic Eradication Therapy of Barrett's Esophagus and Related Neoplasia

Affiliations
Practice Guideline

AGA Clinical Practice Guideline on Endoscopic Eradication Therapy of Barrett's Esophagus and Related Neoplasia

Joel H Rubenstein et al. Gastroenterology. 2024 Jun.

Abstract

Background & aims: Barrett's esophagus (BE) is the precursor to esophageal adenocarcinoma (EAC). Endoscopic eradication therapy (EET) can be effective in eradicating BE and related neoplasia and has greater risk of harms and resource use than surveillance endoscopy. This clinical practice guideline aims to inform clinicians and patients by providing evidence-based practice recommendations for the use of EET in BE and related neoplasia.

Methods: The Grading of Recommendations Assessment, Development and Evaluation framework was used to assess evidence and make recommendations. The panel prioritized clinical questions and outcomes according to their importance for clinicians and patients, conducted an evidence review, and used the Evidence-to-Decision Framework to develop recommendations regarding the use of EET in patients with BE under the following scenarios: presence of (1) high-grade dysplasia, (2) low-grade dysplasia, (3) no dysplasia, and (4) choice of stepwise endoscopic mucosal resection (EMR) or focal EMR plus ablation, and (5) endoscopic submucosal dissection vs EMR. Clinical recommendations were based on the balance between desirable and undesirable effects, patient values, costs, and health equity considerations.

Results: The panel agreed on 5 recommendations for the use of EET in BE and related neoplasia. Based on the available evidence, the panel made a strong recommendation in favor of EET in patients with BE high-grade dysplasia and conditional recommendation against EET in BE without dysplasia. The panel made a conditional recommendation in favor of EET in BE low-grade dysplasia; patients with BE low-grade dysplasia who place a higher value on the potential harms and lower value on the benefits (which are uncertain) regarding reduction of esophageal cancer mortality could reasonably select surveillance endoscopy. In patients with visible lesions, a conditional recommendation was made in favor of focal EMR plus ablation over stepwise EMR. In patients with visible neoplastic lesions undergoing resection, the use of either endoscopic mucosal resection or endoscopic submucosal dissection was suggested based on lesion characteristics.

Conclusions: This document provides a comprehensive outline of the indications for EET in the management of BE and related neoplasia. Guidance is also provided regarding the considerations surrounding implementation of EET. Providers should engage in shared decision making based on patient preferences. Limitations and gaps in the evidence are highlighted to guide future research opportunities.

Keywords: Barrett’s Esophagus; Cryosurgery; Endoscopic Mucosal Resection; Esophageal Neoplasms; Radiofrequency Ablation.

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Conflict of interest statement

Panel members disclosed all potential conflicts of interest. Conflicts were managed according to AGA policies, the National Academy of Medicine, and Guidelines International Network standards.- Development of this guideline was wholly funded by the AGA with no support from the industry.

Potential Conflicts of Interest:

JHR has received research funding from Lucid Diagnostics. DK has received funding for consultation for Medtronic. Shailendra Singh has received funding for consultation from Boston Scientific and Fujifilm Endoscopy. SW has received funding for consultation to Exact Sciences, Lucid, Enterotracker and research support from Lucid, CDx Diagnostics and Exact Sciences. Siddharth Singh has received research funding from Pfizer. SS, AKC, AP, TS, APT, SE, RP, PD, and JMI had no conflicts of interest.

Figures

Figure 1.1
Figure 1.1
Forest plot RCTs comparing progression to EAC among patients with LGD who were treated with EET compared to endoscopic surveillance alone
Figure 1.2.
Figure 1.2.
Forest plot of RCTs comparing progression to HGD or EAC among patients with LGD who were treated with EET compared to endoscopic surveillance alone
Figure 1.3.
Figure 1.3.
Forest plot from observational studies of pooled incidence rate of progression to EAC per patient-year among patients with LGD treated with EET.
Figure 1.4.
Figure 1.4.
Forest plot from observational studies of pooled incidence rate of progression to EAC or HGD per patient-year among patients with LGD treated with EET.
Figure 2.1.
Figure 2.1.
Forest plot of comparative studies comparing EAC at 1-2 years follow-up for patients treated with EMR vs ESD.
Figure 2.2.
Figure 2.2.
Forest plot of comparative studies comparing R0 resection among patients treated with EMR vs ESD.
Figure 2.3.
Figure 2.3.
Forest plot of comparative studies comparing CEN among patients treated with EMR vs ESD.
Figure 2.4.
Figure 2.4.
Forest plot of comparative studies comparing CEIM among patients treated with EMR vs ESD.
Figure 3.1.
Figure 3.1.
Forest plot of pooled proportion of stricture formation among patients with BE and visible lesion treated with ESD.
Figure 3.2.
Figure 3.2.
Forest plot of direct comparative studies comparing stricture formation in patients with BE and visible lesion treated with EMR vs ESD.
Figure 4.1.
Figure 4.1.
Forest plot of pooled proportion of major bleeding events among patients with BE and visible lesion treated with ESD.
Figure 4.2.
Figure 4.2.
Forest plot of direct comparative studies comparing major bleeding in patients with BE and visible lesion treated with EMR vs ESD.
Figure 5.1.
Figure 5.1.
Forest plot of pooled proportion of perforation among patients with BE and visible lesion treated with ESD.
Figure 5.2.
Figure 5.2.
Forest plot of direct comparative studies comparing perforation in patients with BE and visible lesion treated with EMR vs ESD.

References

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