作者
Amir M. Khoshiwal,Nicola Frei,Roos E. Pouw,Christian Smolko,Meenakshi Arora,Jennifer J. Siegel,Lucas C. Duits,Rebecca J. Critchley-Thorne,Jacques Bergman,John R. Goldblum,Elizabeth Montgomery,Jon M. Davison,Jagjit Singh,Jared Szymanski,Anthony S. Perry,Cornelis A. Seldenrijk,Fiebo Ten Kate,G. Johan A. Offerhaus,Paul Drillenberg,Casper Jansen,Natalja Leeuwis-Fedorovic,Runjan Chetty,Roger Feakins,Marnix Jansen,Catherine N. Chinyama,Edwin Cooper,Reza Vaziri,Gustavo Baretton,Andrea Tannapfel,Michael Vieth,Bálint Melcher,Ildikó Mesteri,Heiko Müller,Petra Wetzel,Gert De Hertogh,Anne Hoorens,Stepanie Verschuere,An Tamsin,Kevin Wetzels,Marie-Astrid Van Caillie
摘要
Background & Aims
Low-grade dysplasia (LGD) is associated with an increased risk of progression in Barrett's esophagus (BE); however, the diagnosis of LGD is limited by substantial interobserver variability. Multiple studies have shown that an objective tissue systems pathology test (TissueCypher Barrett's Esophagus Test, TSP-9), can effectively predict neoplastic progression in patients with BE. This study aimed to compare the risk stratification performance of the TSP-9 test vs benchmarks of generalist and expert pathology. Methods
A blinded cohort study was conducted in the screening cohort of a randomized controlled trial of patients with BE with community-based LGD. Biopsies from the first endoscopy with LGD were assessed by the TSP-9 test and independently reviewed by 30 pathologists from 5 countries per standard practice. The accuracy of the test and the diagnoses in predicting high-grade dysplasia (HGD) and esophageal adenocarcinoma (EAC) were compared. Results
A total of 154 patients with BE (122 men), mean age 60.9 ± 9.8 years were studied. Twenty-four patients progressed to HGD/EAC within 5 years (median time of 1.7 years) and 130 did not progress to HGD/EAC within 5 years (median 7.8 years follow-up). The TSP-9 test demonstrated higher sensitivity (71% vs mean 63%, range 33%–88% across 30 pathologists), than the pathology review in detecting patients who progressed (P = .01186). Conclusions
The TSP-9 test outperformed the pathologists in risk stratifying patients with BE with LGD. Care guided by the test can provide an effective solution to variable pathology review of LGD, improving health outcomes by upstaging care to therapeutic intervention for patients at high risk for progression, while reducing unnecessary interventions in low-risk patients.