A Tissue Systems Pathology Test Outperforms the Standard-of-Care Variables in Predicting Progression in Patients With Barrett's Esophagus

Author:

Davison Jon M.1,Goldblum John R.2,Duits Lucas C.3,Khoshiwal Amir M.3,Bergman Jacques J.3,Falk Gary W.4,Diehl David L.5,Khara Harshit S.5,Smolko Christian6,Arora Meenakshi6,Siegel Jennifer J.6,Critchley-Thorne Rebecca J.6ORCID,Thota Prashanthi N.2

Affiliation:

1. University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA;

2. Cleveland Clinic, Cleveland, Ohio, USA;

3. Amsterdam University Medical Centers, Amsterdam, The Netherlands;

4. Perelman School of Medicine University of Pennsylvania, Philadelphia, Pennsylvania, USA;

5. Geisinger Medical Center, Danville, Pennsylvania, USA;

6. Castle Biosciences, Inc., Pittsburgh, Pennsylvania, USA.

Abstract

INTRODUCTION: Objective risk stratification is needed for patients with Barrett's esophagus (BE) to enable risk-aligned management to improve health outcomes. This study evaluated the predictive performance of a tissue systems pathology [TSP-9] test (TissueCypher) vs current clinicopathologic variables in a multicenter cohort of patients with BE. METHODS: Data from 699 patients with BE from 5 published studies on the TSP-9 test were evaluated. Five hundred nine patients did not progress during surveillance, 40 were diagnosed with high-grade dysplasia/esophageal adenocarcinoma (HGD/EAC) within 12 months, and 150 progressed to HGD/EAC after 12 months. Age, sex, segment length, hiatal hernia, original and expert pathology review diagnoses, and TSP-9 risk classes were collected. The predictive performance of clinicopathologic variables and the TSP-9 test was compared, and the TSP-9 test was evaluated in clinically relevant patient subsets. RESULTS: The sensitivity of the TSP-9 test in detecting progressors was 62.3% compared with 28.3% for expert-confirmed low-grade dysplasia (LGD), while the original diagnosis abstracted from medical records did not provide any significant risk stratification. The TSP-9 test identified 57% of progressors with nondysplastic Barrett's esophagus (NDBE) (P < 0.0001). Patients with NDBE who scored TSP-9 high risk progressed at a similar rate (3.2%/yr) to patients with expert-confirmed LGD (3.7%/yr). The TSP-9 test provided significant risk stratification in clinically low-risk patients (NDBE, female, short-segment BE) and clinically high-risk patients (IND/LGD, male, long-segment BE) (P < 0.0001 for comparison of high-risk classes vs low-risk classes). DISCUSSION: The TSP-9 test predicts risk of progression to HGD/EAC independently of current clinicopathologic variables in patients with BE. The test provides objective risk stratification results that may guide management decisions to improve health outcomes for patients with BE.

Funder

Castle Biosciences, Inc.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology

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