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The Tissue Systems Pathology Test Objectively Risk-Stratifies Patients With Barrett's Esophagus: Results From a Multicenter US Clinical Experience Study.
Villa, Nicolas A; Ordonez-Castellanos, Miguel; Yodice, Michael; Newhams, Kirsten; Ayazi, Shahin; Smolko, Christian; Arora, Meenakshi; Critchley-Thorne, Rebecca J; Khara, Harshit S; Diehl, David L.
Afiliação
  • Villa NA; MultiCare Rockwood Digestive Health Center, Spokane, WA.
  • Ordonez-Castellanos M; MultiCare Rockwood Digestive Health Center, Spokane, WA.
  • Yodice M; Department of Gastroenterology and Hepatology, Geisinger Medical Center, Danville, PA.
  • Newhams K; West Penn Hospital, Allegheny Health Network.
  • Ayazi S; West Penn Hospital, Allegheny Health Network.
  • Smolko C; Research and Development, Castle Biosciences, Inc., Pittsburgh, PA.
  • Arora M; Research and Development, Castle Biosciences, Inc., Pittsburgh, PA.
  • Critchley-Thorne RJ; Research and Development, Castle Biosciences, Inc., Pittsburgh, PA.
  • Khara HS; Department of Gastroenterology and Hepatology, Geisinger Medical Center, Danville, PA.
  • Diehl DL; Department of Gastroenterology and Hepatology, Geisinger Medical Center, Danville, PA.
J Clin Gastroenterol ; 2024 Jul 02.
Article em En | MEDLINE | ID: mdl-38954407
ABSTRACT

BACKGROUND:

Barrett's esophagus (BE) is a diagnosis of esophageal intestinal metaplasia, which can progress to esophageal adenocarcinoma (EAC), and guidelines recommend endoscopic surveillance for early detection and treatment of EAC. However, current practices have limited effectiveness in risk-stratifying patients with BE.

AIM:

This study aimed to evaluate use of the TSP-9 test in risk-stratifying clinically relevant subsets of patients with BE in clinical practice.

METHODS:

TSP-9 results for tests ordered by 891 physicians for 8080 patients with BE with clinicopathologic data were evaluated. Orders were from nonacademic (94.3%) and academic (5.7%) settings for nondysplastic BE (NDBE; n=7586; 93.9%), indefinite for dysplasia (IND, n=312, 3.9%), and low-grade dysplasia (LGD, n=182, 2.3%).

RESULTS:

The TSP-9 test scored 83.2% of patients with low risk, 10.6% intermediate risk, and 6.2% high risk, respectively, for progression to HGD/EAC within 5 years. TSP-9 provided significant risk-stratification independently of clinicopathologic features, within NDBE, IND, and LGD subsets, male and female, and short- and long-segment subsets of patients. TSP-9 identified 15.3% of patients with NDBE as intermediate/high-risk for progression, which was 6.4 times more than patients with a pathology diagnosis of LGD. Patients with NDBE who scored intermediate or high risk had a predicted 5-year progression risk of 8.1% and 15.3%, respectively, which are similar to and higher than published progression rates in patients with BE with confirmed LGD.

CONCLUSIONS:

The TSP-9 test identified a high-risk subset of patients with NDBE who were predicted to progress at a higher rate than confirmed LGD, enabling early detection of patients requiring management escalation to reduce the incidence of EAC. TSP-9 scored the majority of patients with NDBE as low risk, providing support to adhere to 3- to 5-year surveillance per guidelines.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article