Departments of Gastroenterology and Hepatology.
Pathology, Academic Medical Center, Amsterdam.
Dis Esophagus. 2019 Nov 13;32(9). doi: 10.1093/dote/doy037.
Patient selection is suboptimal in most studies focused on identifying biological markers for neoplastic progression in Barrett's esophagus (BE). This study aims to describe a stringently selected community-based case-control cohort of non-dysplastic BE (NDBE) patients who progressed to high-grade dysplasia (HGD) or esophageal adenocarcinoma (EAC) and BE patients who never progressed to be used for future biomarker studies. We identified all patients referred for endoscopic work-up of BE neoplasia at three tertiary referral centers for treatment of BE neoplasia between 2000 and 2013. We performed a detailed registration of any endoscopic surveillance history before neoplastic progression. Controls were selected from a retrospective BE surveillance registration in 10 community hospitals. A total of 887 patients were referred for endoscopic work-up of BE neoplasia. Based on predefined selection criteria, we identified 165 progressor patients (82% men; mean age 55 years ± 10.4) with a baseline endoscopy demonstrating NDBE > 2 years before neoplastic progression. Using the same predefined selection criteria, 723 nonprogressor patients (67% men; mean age 57 years ± 11.3) with >2 years of endoscopic surveillance were identified. Median length of the BE segment was 5 cm (IQR 4-7) in progressors and 4 cm (IQR 2-6) in controls. Median duration of surveillance was 89 months (IQR 54-139) in progressors and 76 months (IQR 47-116) in nonprogressors. Paraffin embedded biopsies are available for biomarker research in all patients. Ethical approval was obtained and material transfer agreements were signed with all 58 contributing pathology labs. This is the largest community-based case-control cohort of BE patients with and without progression to early neoplasia. The stringent selection criteria and the availability of paraffin embedded biopsy specimens make this a unique cohort for biomarker studies.
大多数聚焦于在巴雷特食管(BE)中识别肿瘤进展的生物标志物的研究中,患者选择都不够理想。本研究旨在描述一个严格选择的、基于社区的非异型增生 BE(NDBE)患者病例对照队列,这些患者进展为高级别异型增生(HGD)或食管腺癌(EAC),以及从未进展为 BE 的患者,用于未来的生物标志物研究。我们在 2000 年至 2013 年间,在三个三级转诊中心识别出所有因 BE 肿瘤性疾病而行内镜检查的患者。我们详细登记了在肿瘤进展前的任何内镜监测史。对照组从 10 家社区医院的 BE 监测登记中回顾性选择。共有 887 名患者因 BE 肿瘤性疾病而行内镜检查。根据预设的选择标准,我们确定了 165 名进展患者(82%为男性;平均年龄 55 岁 ± 10.4 岁),基线内镜显示 NDBE 在肿瘤进展前超过 2 年。使用相同的预设选择标准,我们确定了 723 名非进展患者(67%为男性;平均年龄 57 岁 ± 11.3 岁),他们的内镜监测时间超过 2 年。进展患者的 BE 段长度中位数为 5cm(IQR 4-7),对照组为 4cm(IQR 2-6)。进展患者的监测中位时间为 89 个月(IQR 54-139),非进展患者为 76 个月(IQR 47-116)。所有患者均有用于生物标志物研究的石蜡包埋活检。获得了伦理批准,并与所有 58 个参与的病理实验室签署了材料转移协议。这是最大的基于社区的 BE 患者病例对照队列,包括有和没有早期肿瘤进展的患者。严格的选择标准和石蜡包埋活检标本的可用性使该队列成为生物标志物研究的独特资源。