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Risk of malignant progression in Barrett's esophagus indefinite for dysplasia.

作者信息

Ma M, Shroff S, Feldman M, DeMarshall M, Price C, Tierney A, Falk G W

机构信息

Department of Medicine, Hospital of the University of Pennsylvania, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA.

Department of Pathology and Laboratory Medicine at the Hospital of the University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Dis Esophagus. 2017 Mar 1;30(3):1-5. doi: 10.1093/dote/dow025.


DOI:10.1093/dote/dow025
PMID:28184470
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6036655/
Abstract

Barrett's esophagus is a well-recognized risk factor for esophageal adenocarcinoma. The natural history of Barrett's esophagus classified as ‘indefinite for dysplasia’ (IND) is poorly characterized. The aim of this study is to characterize the natural history of IND by determining the rate of neoplastic progression and identifying risk factors for progression. Patients from the University of Pennsylvania Health System pathology database and Barrett's esophagus registry with a diagnosis of IND between 2000 and 2014 were identified. Exclusion criteria included: (1) prior diagnosis of low-grade dysplasia (LGD), high-grade dysplasia (HGD), or esophageal adenocarcinoma (EAC); (2) presence of LGD, HGD, or EAC at the time of diagnosis of IND; and (3) lack of follow-up endoscopy after diagnosis. Patients with neoplastic progression were classified as having either prevalent disease (LGD, HGD, or EAC on surveillance biopsy within 12 months of IND diagnosis) or incident disease (LGD, HGD, or EAC on surveillance biopsy >12 months after IND diagnosis). One hundred six patients were eligible for analysis. Of 87 patients with follow-up endoscopy and biopsies within 1 year of IND diagnosis, 7 (8%) had prevalent disease (2 LGD, 4 HGD, 1 EAC). The prevalence of LGD was 2.3%, HGD was 4.6%, and EAC was 1.1%. Importantly, four of the seven prevalent (2 LGD, 2 HGD) cases were found to have dysplasia within 6 months of IND diagnosis. No demographic or endoscopic characteristics studied were associated with prevalent disease. Of the 106 IND patients, there were 66 patients without prevalent dysplasia with >1-year follow-up. Three (4.5%) progressed (1 to LGD after 12 months, 2 to HGD after 16.5 and 28 months), yielding an incidence rate for any dysplasia of 1.4 cases/100 person-years and HGD/EAC of 0.9/100 person-years. Risk factors for incident disease were smoking (p = 0.02) and Barrett's esophagus segment length (p = 0.03). IND is associated with considerable risk of prevalent dysplasia, especially within the first 6 months after diagnosis. However, the incidence of HGD/EAC is low and similar to previous studies of IND. These data suggest that IND patients should have repeat endoscopy within 6 months with careful surveillance protocols. Longer BE length and smoking history may help predict which patients are more likely to develop dysplasia, and therefore identify patients who may warrant even closer monitoring.

摘要

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引用本文的文献

[1]
The utility of P53 immunohistochemistry in the diagnosis of Barrett's oesophagus with indefinite for dysplasia.

Histopathology. 2022-6

[2]
The risk of neoplasia in patients with Barrett's esophagus indefinite for dysplasia: a multicenter cohort study.

Gastrointest Endosc. 2021-8

[3]
Mutational load may predict risk of progression in patients with Barrett's oesophagus and indefinite for dysplasia: a pilot study.

BMJ Open Gastroenterol. 2019-2-2

本文引用的文献

[1]
ACG Clinical Guideline: Diagnosis and Management of Barrett's Esophagus.

Am J Gastroenterol. 2016-1

[2]
Clinical outcomes in patients with a diagnosis of "indefinite for dysplasia" in Barrett's esophagus: a multicenter cohort study.

Endoscopy. 2015-8

[3]
BOB CAT: A Large-Scale Review and Delphi Consensus for Management of Barrett's Esophagus With No Dysplasia, Indefinite for, or Low-Grade Dysplasia.

Am J Gastroenterol. 2015-5

[4]
Risk of neoplastic progression in Barrett's esophagus diagnosed as indefinite for dysplasia: a nationwide cohort study.

Endoscopy. 2014-12-18

[5]
Risk stratification of patients with barrett's esophagus and low-grade dysplasia or indefinite for dysplasia.

Clin Gastroenterol Hepatol. 2014-8-4

[6]
Risk for esophageal neoplasia in Barrett's esophagus patients with mucosal changes indefinite for dysplasia.

J Gastroenterol Hepatol. 2015-2

[7]
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Gut. 2013-10-28

[8]
Trends in esophageal adenocarcinoma incidence and mortality.

Cancer. 2012-12-11

[9]
The role of endoscopy in Barrett's esophagus and other premalignant conditions of the esophagus.

Gastrointest Endosc. 2012-12

[10]
The significance of "indefinite for dysplasia" grading in Barrett metaplasia.

Arch Pathol Lab Med. 2011-4

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