Wilson Natalie J, Mordan Nicholas, Potrock Cole, Shaheen Nicholas J
Division of Gastroenterology and Hepatology, Center for Esophageal Diseases and Swallowing, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Am J Gastroenterol. 2025 Aug 28. doi: 10.14309/ajg.0000000000003753.
Barrett's esophagus (BE) is the only known histological precursor to esophageal adenocarcinoma (EAC). The incidence of EAC has risen significantly over the past four decades in the United States and other Western countries, and the prognosis of EAC remains poor, with over half of individuals diagnosed at a late stage. Despite this, fewer than one in five eligible individuals undergo endoscopic screening for BE. Current screening practices rely on upper endoscopy, limiting widespread adoption and missing a significant portion of at-risk individuals. Recent technological advancements in minimally invasive screening modalities have the potential to expand screening efforts, improve detection rates, and reduce healthcare resource utilization. This review discusses the conceptual underpinnings and hurdles to successful screening for EAC and BE, evaluates newer technologies for screening, including non-endoscopic cell collection devices, blood-based biomarkers, transnasal endoscopy, and exhaled volatile organic compounds, and examines emerging methods for enhancing detection of dysplasia and intestinal metaplasia, including artificial intelligence and Wide Area Transepithelial Sampling. The value of screening in light of a recent randomized trial of surveillance from the UK, as well as a landmark study on non-endoscopic risk stratification for dysplasia in BE, are considered. While direct evidence linking screening to reduced EAC mortality is lacking, trials highlight promising outcomes in early detection of precancerous and cancerous lesions. Future directions, challenges, and recommendations for optimizing BE screening are discussed.
巴雷特食管(BE)是已知的食管腺癌(EAC)唯一的组织学前驱病变。在美国和其他西方国家,EAC的发病率在过去四十年中显著上升,且EAC的预后仍然很差,超过一半的患者在晚期才被诊断出来。尽管如此,符合条件的个体中接受BE内镜筛查的不到五分之一。目前的筛查方法依赖于上消化道内镜检查,这限制了其广泛应用,并且遗漏了很大一部分高危个体。微创筛查方式的最新技术进展有可能扩大筛查范围,提高检出率,并减少医疗资源的利用。本文综述讨论了成功筛查EAC和BE的概念基础及障碍,评估了包括非内镜细胞采集装置、血液生物标志物、经鼻内镜检查和呼出挥发性有机化合物在内的新型筛查技术,并探讨了增强发育异常和肠化生检测的新兴方法,包括人工智能和广域经上皮采样。还考虑了根据英国最近一项监测随机试验以及一项关于BE发育异常非内镜风险分层的里程碑式研究得出的筛查价值。虽然缺乏将筛查与降低EAC死亡率直接联系起来的证据,但试验突出了在癌前病变和癌性病变早期检测方面的有前景的结果。本文还讨论了优化BE筛查的未来方向、挑战和建议。