Center for Clinical Management Research, Lieutenant Colonel Charles S. Kettles Veterans Affairs Medical Center, Ann Arbor, Michigan; Barrett's Esophagus Program, Division of Gastroenterology, University of Michigan Medical School, Ann Arbor, Michigan; Cancer Control and Population Sciences Program, Rogel Cancer Center, University of Michigan Medical School, Ann Arbor, Michigan.
Division of Digestive and Liver Disease, University of Texas Southwestern, Dallas, Texas.
Gastroenterology. 2024 Jun;166(6):1020-1055. doi: 10.1053/j.gastro.2024.03.019.
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.
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.
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.
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.
巴雷特食管(BE)是食管腺癌(EAC)的前身。内镜下消除治疗(EET)可以有效消除 BE 和相关肿瘤,并比内镜监测具有更大的危害和资源使用风险。本临床实践指南旨在通过提供 EET 在 BE 和相关肿瘤中的使用的循证实践建议来为临床医生和患者提供信息。
使用推荐评估、制定和评估(GRADE)框架评估证据并提出建议。专家组根据对临床医生和患者的重要性对临床问题和结果进行了优先级排序,进行了证据审查,并使用证据决策框架制定了关于以下情况下 EET 在 BE 患者中的使用建议:(1)高级别异型增生,(2)低级别异型增生,(3)无异型增生,(4)逐步内镜黏膜切除术(EMR)或局灶性 EMR 加消融的选择,以及(5)内镜黏膜下剥离术与 EMR。临床建议基于理想效果和不良效果、患者价值观、成本和健康公平考虑之间的平衡。
专家组就 EET 在 BE 和相关肿瘤中的使用达成了 5 项建议。基于现有证据,专家组强烈建议在 BE 高级别异型增生患者中使用 EET,并有条件反对在 BE 无异型增生患者中使用 EET。专家组建议有条件支持在 BE 低级别异型增生患者中使用 EET;对潜在危害的重视程度较高,对降低食管癌死亡率的益处(不确定)的重视程度较低的 BE 低级别异型增生患者可以合理选择内镜监测。对于可见病变的患者,建议有条件地支持局灶性 EMR 加消融而不是逐步 EMR。对于进行切除的可见肿瘤性病变患者,根据病变特征建议使用内镜黏膜切除术或内镜黏膜下剥离术。
本文件全面概述了 EET 在 BE 和相关肿瘤管理中的适应证。还提供了有关 EET 实施相关考虑的指导。提供者应根据患者的偏好进行共同决策。突出了证据中的局限性和差距,以指导未来的研究机会。