4.7 Article

Prediction of Progression in Barrett's Esophagus Using a Tissue Systems Pathology Test: A Pooled Analysis of International Multicenter Studies

期刊

CLINICAL GASTROENTEROLOGY AND HEPATOLOGY
卷 20, 期 12, 页码 2772-+

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cgh.2022.02.033

关键词

Biomarker; Esophageal Cancer; Screening; Surveillance

资金

  1. National Cancer Institute, United States [RO1 CA241164]
  2. Cernostics Inc.

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This study evaluates the adjunct value of a tissue systems pathology test in predicting the progression risk in Barrett's esophagus (BE). The results show that the high-risk class of TissueCypher can independently predict the risk of progression to high-grade dysplasia/adenocarcinoma in BE patients and improve the predictive ability compared to using clinical variables alone.
BACKGROUND & AIMS: Prediction of progression risk in Barrett's esophagus (BE) may enable personalized management. We aimed to assess the adjunct value of a tissue systems pathology test (TissueCypher) performed on paraffin-embedded biopsy tissue, when added to expert pathology review in predicting incident progression, pooling individual patient-level data from multiple international studies METHODS: Demographics, clinical features, the TissueCypher risk class/score, and progression status were analyzed. Conditional logistical regression analysis was used to develop multivariable models predicting incident progression with and without the TissueCypher risk class (low, intermediate, high). Concordance (c-) statistics were calculated and compared with likelihood ratio tests to assess predictive ability of models. A risk prediction calculator integrating clinical variables and TissueCypher risk class was also developed. RESULTS: Data from 552 patients with baseline no (n [ 472), indefinite (n [ 32), or low-grade dysplasia (n [ 48) (comprising 152 incident progressors and 400 non-progressors) were analyzed. A high-risk test class independently predicted increased risk of progression to high-grade dysplasia/adenocarcinoma (odds ratio, 6.0; 95% confidence interval, 2.9-12.0), along with expert confirmed low-grade dysplasia (odds ratio, 2.9; 95% confidence interval, 1.2-7.2). Model prediction of progression with the TissueCypher risk class incorporated was significantly superior than without, in the whole cohort (c-statistic 0.75 vs 0.68; P < .0001) and the nondysplastic BE subset (c-statistic 0.72 vs 0.63; P < .0001). Sensitivity and specificity of the high risk TissueCypher class were 38% and 94%, respectively. CONCLUSIONS: An objective tissue systems pathology test high-risk class is a strong independent predictor of incident progression in patients with BE, substantially improving progression risk prediction over clinical variables alone. Although test specificity was high, sensitivity was modest.

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