Incidence of Progression of Persistent Nondysplastic Barrett’s Esophagus to Malignancy

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 subse...

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Veröffentlicht in:Clinical gastroenterology and hepatology 2019-04, Vol.17 (5), p.869-877.e5
Hauptverfasser: Peters, Yonne, Honing, Judith, Kievit, Wietske, Kestens, Christine, Pestman, Wiebe, Nagtegaal, Iris D., van der Post, Rachel S., Siersema, Peter D.
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container_end_page 877.e5
container_issue 5
container_start_page 869
container_title Clinical gastroenterology and hepatology
container_volume 17
creator Peters, Yonne
Honing, Judith
Kievit, Wietske
Kestens, Christine
Pestman, Wiebe
Nagtegaal, Iris D.
van der Post, Rachel S.
Siersema, Peter D.
description 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. 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. 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). 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.
doi_str_mv 10.1016/j.cgh.2018.08.033
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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. 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. 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). 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. 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subjects Biomarker
Epidemiology
PALGA
Prognostic Factor
Risk Factor
title Incidence of Progression of Persistent Nondysplastic Barrett’s Esophagus to Malignancy
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