Oesophageal cell collection device and biomarker testing to identify high-risk Barrett's patients requiring endoscopic investigation

Abstract Background Barrett's oesophagus surveillance places significant burden on endoscopy services yet is vital to detect early cancerous change. Oesophageal cell collection device (OCCD) testing was introduced across Scotland for Barrett's surveillance in response to the COVID-19 pande...

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Veröffentlicht in:British journal of surgery 2024-05, Vol.111 (5)
Hauptverfasser: Chien, Siobhan, Glen, Paul, Penman, Ian, Cruickshank, Neil, Bryce, Gavin, Crumley, Andrew, Phull, Perminder, Miller, Michael, Fletcher, Jonathan, Gunjaca, Ivan, Apollos, Jeyakumar, Robertson, Kevin, Fullarton, Grant
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Sprache:eng
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Zusammenfassung:Abstract Background Barrett's oesophagus surveillance places significant burden on endoscopy services yet is vital to detect early cancerous change. Oesophageal cell collection device (OCCD) testing was introduced across Scotland for Barrett's surveillance in response to the COVID-19 pandemic. This national pragmatic retrospective study presents the CytoSCOT programme results and evaluates whether OCCD testing is successfully identifying high-risk Barrett's patients requiring urgent endoscopy. Methods All patients undergoing OCCD testing for Barrett's surveillance across 11 Scottish health boards over a 32-month period were identified. Patients who underwent endoscopy within 12 months of OCCD test were included. Individual patient records were interrogated to record clinical information and OCCD test result to categorize patients into risk groups. Endoscopic histopathology results were analysed according to risk group and segment length. Patients were deemed high risk if the OCCD test demonstrated atypia and/or p53 positivity. Results 4204 OCCD tests were performed in 3745 patients: 608 patients underwent endoscopy within 12 months and were included in this analysis. Patients with longer Barrett's segments were significantly more likely to have an abnormal OCCD test. 50/608 patients (8.2%) had high-grade dysplasia or cancer on endoscopic biopsies: this equates to 1.3% of the total group (50/3745). 46/50 patients (92.0%) were deemed high risk, triggering urgent endoscopy: this rose to 100% with insufficient tests removed. There were no cancers diagnosed within 12 months post-OCCD in the low-risk group. Conclusion OCCD testing is an effective triage tool to identify high-risk patients with Barrett's oesophagus requiring further investigation with endoscopy within the real-world setting. Oesophageal cell collection device (OCCD) testing has shown promising trial results in the diagnosis of Barrett's oesophagus. This study presents the first real-world data to show that OCCD testing demonstrates sound diagnostic accuracy as a triage tool in highlighting high-risk Barrett's surveillance patients requiring urgent upper gastrointestinal endoscopy.
ISSN:0007-1323
1365-2168
DOI:10.1093/bjs/znae117