Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Medical Research Council Cancer Unit, Hutchison/Medical Research Council Research Centre, University of Cambridge, Cambridge, United Kingdom.
Clin Gastroenterol Hepatol. 2022 Aug;20(8):1709-1718. doi: 10.1016/j.cgh.2021.10.039. Epub 2021 Oct 29.
BACKGROUND & AIMS: Despite extensive Barrett's esophagus (BE) screening efforts, most patients with esophageal adenocarcinoma (EAC) present de novo. It is unclear how much of this problem is the result of insensitivity or poor applications of current screening guidelines. We aimed to evaluate the sensitivity of guidelines by determining the proportion of prevalent EAC cases that meet the American College of Gastroenterology (ACG) or the British Society of Gastroenterology (BSG) guidelines for BE screening and determine whether changes to criteria would enhance detection.
A retrospective single-center cohort from the United States (n = 663) and a prospective multicenter cohort from the United Kingdom (n = 645) were collected and analyzed independently. Screening eligibility was determined as patients with chronic reflux and at least 2 or more risk factors as defined by the guidelines. We calculated the proportion of screening-eligible patients and then compared BE/EAC risk factors between screening-eligible and screening-ineligible patients using the chi-squared or Student t test as appropriate.
In the Mayo clinic cohort there were 54.9% EAC cases and in the UK cohort there were 38.9% EAC cases that were not identified by ACG or BSG screening criteria, respectively. Among patients who did not meet the screening criteria, lack of heartburn was observed in 86.5% in the Mayo clinic cohort and in 61.4% in the UK cohort. Other risk factors that were lacking included obesity (defined as a body mass index of ≥30 kg/m) and family history of EAC. Eliminating chronic reflux from the ACG/BSG criteria improved eligibility for screening from 45.1% to 81.3% (P < .001) in the Mayo Clinic cohort and from 61.1% (n = 394) to 81.5% (n = 526; P < .001) in the UK cohort. However, reflux may be difficult to ascertain from the history, and by including proton pump inhibitor use status in addition to the BSG criteria, screening eligibility improved by 10.0% in the UK cohort (n = 459; P < .001).
ACG/BSG BE screening guidelines have limited our ability to detect prevalent EAC. An optimized approach to identifying the individuals most suitable for EAC screening needs to be implemented, particularly one that does not rely on chronic reflux symptoms.
尽管广泛开展了 Barrett 食管(BE)筛查,但大多数食管腺癌(EAC)患者仍为初诊。尚不清楚该问题在多大程度上是由于当前筛查指南的不敏感或应用不当所致。我们旨在通过确定符合美国胃肠病学会(ACG)或英国胃肠病学会(BSG)BE 筛查指南的现患 EAC 病例比例,来评估指南的敏感性,并确定是否改变标准可提高检出率。
我们分别独立收集了美国一个单中心回顾性队列(n=663)和英国一个多中心前瞻性队列(n=645)的数据并进行了分析。筛查合格性的确定标准为:慢性反流且至少符合指南定义的 2 种或更多种危险因素的患者。我们计算了筛查合格性患者的比例,然后使用卡方检验或学生 t 检验比较了筛查合格性和筛查不合格性患者之间的 BE/EAC 危险因素。
在 Mayo 诊所队列中,有 54.9%的 EAC 病例和英国队列中,分别有 38.9%的 EAC 病例未通过 ACG 或 BSG 筛查标准检出。在不符合筛查标准的患者中,Mayo 诊所队列中有 86.5%、英国队列中有 61.4%的患者没有烧心症状。其他缺乏的危险因素包括肥胖(定义为 BMI≥30 kg/m)和 EAC 家族史。将慢性反流从 ACG/BSG 标准中排除后,Mayo 诊所队列的筛查合格性从 45.1%提高到 81.3%(P<0.001),英国队列的筛查合格性从 61.1%(n=394)提高到 81.5%(n=526;P<0.001)。然而,反流可能难以从病史中确定,并且通过将质子泵抑制剂使用情况纳入 BSG 标准,英国队列的筛查合格性提高了 10.0%(n=459;P<0.001)。
ACG/BSG BE 筛查指南限制了我们发现现患 EAC 的能力。需要实施一种优化的方法来识别最适合 EAC 筛查的个体,特别是不依赖慢性反流症状的方法。