Real-world implementation of non-endoscopic triage testing for Barrett’s oesophagus during COVID-19

Author:

Landy R1ORCID,Killcoyne S2,Tang C2,Juniat S2,O’Donovan M23,Goel N2,Gehrung M2,Fitzgerald R C4

Affiliation:

1. Division of Cancer Epidemiology and Genetics, Department of Health and Human Services, National Cancer Institute, National Institutes of Health , Bethesda, MD, USA

2. Cyted Ltd , 22 Station Road , Cambridge CB1 2JD, UK

3. Department of Histopathology, Cambridge University Hospitals NHS Foundation Trust , Cambridge, UK

4. Department of Oncology, Early Cancer Institute, University of Cambridge , Cambridge CB2 0XZ, UK

Abstract

Summary Background The Coronavirus pandemic (COVID-19) curtailed endoscopy services, adding to diagnostic backlogs. Building on trial evidence for a non-endoscopic oesophageal cell collection device coupled with biomarkers (Cytosponge), an implementation pilot was launched for patients on waiting lists for reflux and Barrett’s oesophagus surveillance. Aims (i) To review reflux referral patterns and Barrett’s surveillance practices. (ii) To evaluate the range of Cytosponge findings and impact on endoscopy services. Design and methods Cytosponge data from centralized laboratory processing (trefoil factor 3 (TFF3) for intestinal metaplasia (IM), haematoxylin & eosin for cellular atypia and p53 for dysplasia) over a 2-year period were included. Results A total of 10 577 procedures were performed in 61 hospitals in England and Scotland, of which 92.5% (N = 9784/10 577) were sufficient for analysis. In the reflux cohort (N = 4074 with gastro-oesophageal junction sampling), 14.7% had one or more positive biomarkers (TFF3: 13.6% (N = 550/4056), p53: 0.5% (21/3974), atypia: 1.5% (N = 63/4071)), requiring endoscopy. Among samples from individuals undergoing Barrett’s surveillance (N = 5710 with sufficient gland groups), TFF3-positivity increased with segment length (odds ratio = 1.37 per cm (95% confidence interval: 1.33–1.41, P < 0.001)). Some surveillance referrals (21.5%, N = 1175/5471) had ≤1 cm segment length, of which 65.9% (707/1073) were TFF3 negative. Of all surveillance procedures, 8.3% had dysplastic biomarkers (4.0% (N = 225/5630) for p53 and 7.6% (N = 430/5694) for atypia), increasing to 11.8% (N = 420/3552) in TFF3+ cases with confirmed IM and 19.7% (N = 58/294) in ultra-long segments. Conclusions Cytosponge-biomarker tests enabled targeting of endoscopy services to higher-risk individuals, whereas those with TFF3 negative ultra-short segments could be reconsidered regarding their Barrett’s oesophagus status and surveillance requirements. Long-term follow-up will be important in these cohorts.

Funder

National Institutes of Health

National Cancer Institute

NHS

NHS Scotland for the Implementation Pilots

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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