Incidence of Progression of Persistent Nondysplastic Barrett's Esophagus to Malignancy
Publication year
2019Source
Clinical Gastroenterology and Hepatology, 17, 5, (2019), pp. 869-877.e5ISSN
Publication type
Article / Letter to editor
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Organization
Gastroenterology
Otorhinolaryngology
Health Evidence
IQ Healthcare
Pathology
Journal title
Clinical Gastroenterology and Hepatology
Volume
vol. 17
Issue
iss. 5
Page start
p. 869
Page end
p. 877.e5
Subject
Radboudumc 14: Tumours of the digestive tract RIHS: Radboud Institute for Health Sciences; Radboudumc 14: Tumours of the digestive tract RIMLS: Radboud Institute for Molecular Life Sciences; Radboudumc 5: Inflammatory diseases RIHS: Radboud Institute for Health Sciences; Gastroenterology - Radboud University Medical Center; Health Evidence - Radboud University Medical Center; Otorhinolaryngology - Radboud University Medical Center; Pathology - Radboud University Medical CenterAbstract
BACKGROUND & AIMS: The risk of esophageal adenocarcinoma (EAC) in patients with non-dysplastic Barrett's esophagus (NDBE) is low, so there is debate over the role of ongoing surveillance for patients with NDBE. It is important to identify patients at low risk for progression. We assessed cancer risk based on the subsequent number of endoscopies showing persistence of NDBE in a nationwide study in the Netherlands. METHODS: In a population-based study, patients with a first diagnosis of NDBE were selected from the Dutch nationwide registry of histopathology. We calculated incidence rates and incidence rate ratios (IRR) for high-grade dysplasia (HGD) and EAC to determine whether the number of endoscopies negative for dysplasia and the persistence of NDBE over time associate with progression to malignancy. RESULTS: We identified 12,728 patients with NDBE during 2003 and 2013. HGD or EAC developed in 436 patients (3.4%) during 64,537 person-years of follow up (median, 4.9 years). The rate of progression to HGD or EAC was 0.68 (95% CI, 0.61-0.74) per 100 person-years. In patients with 2 consecutive endoscopies showing NDBE, the rate of progression to HGD or EAC decreased to 0.55 (95% CI, 0.46-0.64) per 100 person-years (IRR, 0.72; 95% CI, 0.60-0.87). Overall, the incidence of HGD or EAC decreased by 14% for each year of progression-free follow-up (IRR, 0.86; 95% CI, 0.81-0.92). CONCLUSION: In a population-based study in the Netherlands, we found patients with stable NDBE to have a low risk of progression to HGD or EAC. These findings indicate that surveillance intervals might be lengthened or even discontinued in subgroups patients with persistent NDBE.
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- Academic publications [242586]
- Electronic publications [129566]
- Faculty of Medical Sciences [92285]
- Open Access publications [104156]
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