Outcomes of patients with Barrett's oesophagus with low-grade dysplasia undergoing endoscopic surveillance in a tertiary centre: a retrospective cohort study.

Barrett's oesophagus low‐grade dysplasia metaplasia neoplasia oesophageal neoplasm upper gastrointestinal endoscopy

Journal

Internal medicine journal
ISSN: 1445-5994
Titre abrégé: Intern Med J
Pays: Australia
ID NLM: 101092952

Informations de publication

Date de publication:
20 Sep 2024
Historique:
received: 12 10 2023
accepted: 29 08 2024
medline: 20 9 2024
pubmed: 20 9 2024
entrez: 20 9 2024
Statut: aheadofprint

Résumé

Barrett's oesophagus predisposes individuals to oesophageal adenocarcinoma (OAC), with the risk of progression to malignancy increasing with the degree of dysplasia, categorized as either low-grade dysplasia (LGD) or high-grade dysplasia (HGD). The reported incidence of progression to OAC in LGD ranges from 0.02% to 11.43% per annum. In patients with LGD, Australian guidelines recommend 6-monthly endoscopic surveillance. We aimed to describe the surveillance practices within a tertiary centre, and to determine the predictive value of surveillance as well as other risk factors for progression. Endoscopy and pathology databases were searched over a 10-year period to collate all cases of Barrett's oesophagus with LGD. Medical records were reviewed to document patient factors and endoscopic and histologic details. Because follow-up times varied greatly, survival analysis techniques were employed. Fifty-nine patients were found to have LGD. Thirteen patients (22.0%) progressed to either HGD or OAC (10 (16.9%) and three (5.1%) respectively); the annual incidence rates of progression to HGD/OAC and OAC were 5.5% and 1.1% respectively. All patients who developed OAC had non-guideline-adherent surveillance. A Cox model found only two predictors of progression: (i) guideline-adherent surveillance, performed in 16 (27.1%), detected progression to HGD/OAC four times earlier than non-guideline-adherent surveillance (95% confidence interval (CI) = 1.3-12.3; P = 0.016). (ii) The detection of visible lesions at exit endoscopy independently predicted progression (hazard ratio = 6.5; 95% CI = 1.9-22.8; P = 0.003). Barrett's oesophagus with LGD poses a significant risk of progression to HGD/OAC. Guideline-recommended surveillance is effective, but is difficult to adhere to. Clinical predictors for those who are more likely to progress are yet to be defined.

Sections du résumé

BACKGROUND AND AIM OBJECTIVE
Barrett's oesophagus predisposes individuals to oesophageal adenocarcinoma (OAC), with the risk of progression to malignancy increasing with the degree of dysplasia, categorized as either low-grade dysplasia (LGD) or high-grade dysplasia (HGD). The reported incidence of progression to OAC in LGD ranges from 0.02% to 11.43% per annum. In patients with LGD, Australian guidelines recommend 6-monthly endoscopic surveillance. We aimed to describe the surveillance practices within a tertiary centre, and to determine the predictive value of surveillance as well as other risk factors for progression.
METHODS METHODS
Endoscopy and pathology databases were searched over a 10-year period to collate all cases of Barrett's oesophagus with LGD. Medical records were reviewed to document patient factors and endoscopic and histologic details. Because follow-up times varied greatly, survival analysis techniques were employed.
RESULTS RESULTS
Fifty-nine patients were found to have LGD. Thirteen patients (22.0%) progressed to either HGD or OAC (10 (16.9%) and three (5.1%) respectively); the annual incidence rates of progression to HGD/OAC and OAC were 5.5% and 1.1% respectively. All patients who developed OAC had non-guideline-adherent surveillance. A Cox model found only two predictors of progression: (i) guideline-adherent surveillance, performed in 16 (27.1%), detected progression to HGD/OAC four times earlier than non-guideline-adherent surveillance (95% confidence interval (CI) = 1.3-12.3; P = 0.016). (ii) The detection of visible lesions at exit endoscopy independently predicted progression (hazard ratio = 6.5; 95% CI = 1.9-22.8; P = 0.003).
CONCLUSION CONCLUSIONS
Barrett's oesophagus with LGD poses a significant risk of progression to HGD/OAC. Guideline-recommended surveillance is effective, but is difficult to adhere to. Clinical predictors for those who are more likely to progress are yet to be defined.

Identifiants

pubmed: 39301935
doi: 10.1111/imj.16532
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 The Author(s). Internal Medicine Journal published by John Wiley & Sons Australia, Ltd on behalf of Royal Australasian College of Physicians.

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Auteurs

Luke J Vlismas (LJ)

Department of Gastroenterology, Gosford Hospital, Gosford, New South Wales, Australia.
Department of Gastroenterology, John Hunter Hospital, Newcastle, New South Wales, Australia.
Faculty of Health and Medicine, University of Newcastle, Newcastle, New South Wales, Australia.

Michael Potter (M)

Department of Gastroenterology, John Hunter Hospital, Newcastle, New South Wales, Australia.
Faculty of Health and Medicine, University of Newcastle, Newcastle, New South Wales, Australia.

Mark R Loewenthal (MR)

Faculty of Health and Medicine, University of Newcastle, Newcastle, New South Wales, Australia.
Department of Medicine, John Hunter Hospital, Newcastle, New South Wales, Australia.

Katie Wilson (K)

Department of Gastroenterology, John Hunter Hospital, Newcastle, New South Wales, Australia.

Kelleigh Allport (K)

Department of Gastroenterology, John Hunter Hospital, Newcastle, New South Wales, Australia.

Donna Gillies (D)

Surgical Services, John Hunter Hospital, Newcastle, New South Wales, Australia.

Dane Cook (D)

Department of Gastroenterology, John Hunter Hospital, Newcastle, New South Wales, Australia.
Faculty of Health and Medicine, University of Newcastle, Newcastle, New South Wales, Australia.

Stephen Philcox (S)

Department of Gastroenterology, John Hunter Hospital, Newcastle, New South Wales, Australia.
Faculty of Health and Medicine, University of Newcastle, Newcastle, New South Wales, Australia.

Steven Bollipo (S)

Department of Gastroenterology, John Hunter Hospital, Newcastle, New South Wales, Australia.
Faculty of Health and Medicine, University of Newcastle, Newcastle, New South Wales, Australia.

Nicholas J Talley (NJ)

Department of Gastroenterology, John Hunter Hospital, Newcastle, New South Wales, Australia.
Faculty of Health and Medicine, University of Newcastle, Newcastle, New South Wales, Australia.

Classifications MeSH