Literature DB >> 29873685

The Amsterdam ReBus progressor cohort: identification of 165 Barrett's surveillance patients who progressed to early neoplasia and 723 nonprogressor patients.

L C Duits1, E Klaver1, A Bureo Gonzalez1, D F Boerwinkel1, F J W Ten Kate2,3, G J A Offerhaus2,3, S L Meijer2, M Visser2, C A Seldenrijk4, K K Krishnadath1, E J Schoon5, Bas L A M Weusten6, Rosalie C Mallant-Hent7, Roos E Pouw1, Jacques J G H M Bergman1.   

Abstract

Patient selection is suboptimal in most studies focused on identifying biological markers for neoplastic progression in Barrett's esophagus (BE). This study aims to describe a stringently selected community-based case-control cohort of non-dysplastic BE (NDBE) patients who progressed to high-grade dysplasia (HGD) or esophageal adenocarcinoma (EAC) and BE patients who never progressed to be used for future biomarker studies. We identified all patients referred for endoscopic work-up of BE neoplasia at three tertiary referral centers for treatment of BE neoplasia between 2000 and 2013. We performed a detailed registration of any endoscopic surveillance history before neoplastic progression. Controls were selected from a retrospective BE surveillance registration in 10 community hospitals. A total of 887 patients were referred for endoscopic work-up of BE neoplasia. Based on predefined selection criteria, we identified 165 progressor patients (82% men; mean age 55 years ± 10.4) with a baseline endoscopy demonstrating NDBE > 2 years before neoplastic progression. Using the same predefined selection criteria, 723 nonprogressor patients (67% men; mean age 57 years ± 11.3) with >2 years of endoscopic surveillance were identified. Median length of the BE segment was 5 cm (IQR 4-7) in progressors and 4 cm (IQR 2-6) in controls. Median duration of surveillance was 89 months (IQR 54-139) in progressors and 76 months (IQR 47-116) in nonprogressors. Paraffin embedded biopsies are available for biomarker research in all patients. Ethical approval was obtained and material transfer agreements were signed with all 58 contributing pathology labs. This is the largest community-based case-control cohort of BE patients with and without progression to early neoplasia. The stringent selection criteria and the availability of paraffin embedded biopsy specimens make this a unique cohort for biomarker studies.
© The Author(s) 2018. Published by Oxford University Press on behalf of International Society for Diseases of the Esophagus. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  biological markers; esophageal cancer; neoplastic progression

Mesh:

Substances:

Year:  2019        PMID: 29873685     DOI: 10.1093/dote/doy037

Source DB:  PubMed          Journal:  Dis Esophagus        ISSN: 1120-8694            Impact factor:   3.429


  3 in total

Review 1.  Endoscopic eradication therapy for Barrett's oesophagus: state of the art.

Authors:  Jennifer M Kolb; Sachin Wani
Journal:  Curr Opin Gastroenterol       Date:  2020-07       Impact factor: 2.741

2.  The SpaTemp cohort: 168 nondysplastic Barrett's esophagus surveillance patients with and without progression to early neoplasia to evaluate the distribution of biomarkers over space and time.

Authors:  N F Frei; K Konté; L C Duits; E Klaver; F J Ten Kate; G J Offerhaus; S L Meijer; M Visser; C A Seldenrijk; E J Schoon; B L A M Weusten; B E Schenk; R C Mallant-Hent; J J Bergman; R E Pouw
Journal:  Dis Esophagus       Date:  2021-03-08       Impact factor: 2.822

3.  Independent Validation of a Tissue Systems Pathology Assay to Predict Future Progression in Nondysplastic Barrett's Esophagus: A Spatial-Temporal Analysis.

Authors:  Nicola F Frei; Kadère Konte; Emily A Bossart; Katelyn Stebbins; Yi Zhang; Roos E Pouw; Rebecca J Critchley-Thorne; Jacques J G H M Bergman
Journal:  Clin Transl Gastroenterol       Date:  2020-10       Impact factor: 4.396

  3 in total

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