Multicenter, Prospective Trial of Nonendoscopic Biomarker-Driven Detection of Barrett's Esophagus and Esophageal Adenocarcinoma.

IF 8 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY American Journal of Gastroenterology Pub Date : 2024-11-01 Epub Date: 2024-04-30 DOI:10.14309/ajg.0000000000002850
Helen R Moinova, Suman Verma, John Dumot, Ashley Faulx, Prasad G Iyer, Marcia Irene Canto, Jean S Wang, Nicholas J Shaheen, Prashanthi N Thota, Lishan Aklog, Joseph E Willis, Sanford D Markowitz, Amitabh Chak
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引用次数: 0

Abstract

Introduction: Preliminary data suggest that an encapsulated balloon (EsoCheck), coupled with a 2 methylated DNA biomarker panel (EsoGuard), detects Barrett's esophagus (BE) and esophageal adenocarcinoma (EAC) with high accuracy. The initial assay requires sample freezing upon collection. The purpose of this study was to assess a next-generation EsoCheck sampling device and EsoGuard assay in a much-enlarged multicenter study clinically enhanced by using a Clinical Laboratory Improvement Amendments of 1988-compliant assay and samples maintained at room temperature.

Methods: Cases with nondysplastic BE (NDBE), dysplastic BE (indefinite for dysplasia, low-grade dysplasia, high-grade dysplasia), EAC, junctional adenocarcinoma, plus endoscopy controls without esophageal intestinal metaplasia, were prospectively enrolled. Medical assistants at 6 institutions delivered the encapsulated balloon per orally with inflation in the stomach. The inflated balloon sampled the distal 5 cm of the esophagus and then was deflated and retracted into the capsule, preventing sample contamination. EsoGuard bisulfite sequencing assayed levels of methylated vimentin and methylated cyclin A1.

Results: A total of 243 evaluable patients-88 cases (median age 68 years, 78% men, 92% White) and 155 controls (median age 57 years, 41% men, 88% White)-underwent adequate EsoCheck sampling. The mean procedural time was approximately 3 minutes. Cases included 31 with NDBE, 16 with indefinite for dysplasia/low-grade dysplasia, 23 with high-grade dysplasia, and 18 with EAC/junctional adenocarcinoma. Thirty-seven NDBE and dysplastic BE cases (53%) were short-segment BE (<3 cm). Overall sensitivity was 85% (95% confidence interval 0.78-0.93) and specificity was 85% (95% confidence interval 0.79-0.90). Sensitivity for NDBE was 84%. EsoCheck/EsoGuard detected 100% of cancers (n = 18).

Discussion: EsoCheck/EsoGuard demonstrated high sensitivity and specificity in detecting BE and BE-related neoplasia.

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非内窥镜生物标记物驱动的巴雷特食管和食管腺癌检测多中心前瞻性试验。
背景:初步数据表明,封装气球(EsoCheckTM)与两个甲基化 DNA 生物标记物面板(EsoGuardTM)相结合,可高精度检测巴雷特食管(BE)和食管腺癌(EAC)。目的:在一项规模更大的多中心研究中评估新一代 EsoCheck 采样设备和 EsoGuard 检测方法,通过使用符合 CLIA 标准的检测方法和室温保存样本,提高临床检测效果:方法:前瞻性地纳入了非增生异常BE(NDBE)、增生异常BE(不定期=IND、低度增生异常=LGD、高度增生异常=HGD)、EAC、交界性腺癌(JAC)病例,以及无食管肠化生的内镜对照病例。六家机构的医疗助理口服封装球囊,在胃部充气。充气球囊在食管远端 5 厘米处取样,然后放气并缩回囊中,以防止样本污染。EsoGuard 亚硫酸氢盐测序法测定了甲基化波形蛋白(mVIM)和甲基化细胞周期蛋白 A1(mCCNA1)的水平:共有 243 名可评估患者接受了充分的 EsoCheck 采样,其中包括 88 名病例(中位年龄 68 岁,78% 为男性,92% 为白人)和 155 名对照组(中位年龄 57 岁,41% 为男性,88% 为白人)。平均手术时间约为 3 分钟。病例包括 31 例 NDBE、16 例 IND/LGD、23 例 HGD 和 18 例 EAC/JAC。37例(53%)非增生异常和增生异常BE为短节段BE(SSBE;小于3厘米)。总体敏感性为 85%(95% CI=0.78-0.93),特异性为 85%(95% CI=0.79-0.90)。对 NDBE 的敏感性为 84%。EsoCheck/EsoGuard检测出100%的癌症(18例):结论:EsoCheck/EsoGuard检测BE和BE相关肿瘤的灵敏度和特异性都很高。
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来源期刊
American Journal of Gastroenterology
American Journal of Gastroenterology 医学-胃肠肝病学
CiteScore
11.40
自引率
5.10%
发文量
458
审稿时长
12 months
期刊介绍: Published on behalf of the American College of Gastroenterology (ACG), The American Journal of Gastroenterology (AJG) stands as the foremost clinical journal in the fields of gastroenterology and hepatology. AJG offers practical and professional support to clinicians addressing the most prevalent gastroenterological disorders in patients.
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