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DOI: 10.1055/a-2634-7895
Clinical decision tree for optimizing endoscopic assessment of signet ring cell carcinoma in hereditary diffuse gastric cancer surveillance
Supported by: Addenbrookes Charitable Trust 300132
Supported by: Medical Research Council G111260
Supported by: Cancer Research UK EDDPJT-Nov23/100006
M. di Pietro is funded by the UK Medical Research Council .
M. di Pietro received additional funds from the Cancer Research UK Cambridge Centre.
L. Wu was funded by the Postdoctoral Program of the Chinese Scholarship Council (grant number 202206275012).
L. Wu was funded by the CRUK grant EDDPJT-Nov23/100006
C.Y.C. Lee is funded by the Gates Cambridge Trust.
C.Y.C. Lee is funded the University of Cambridge School of Clinical Medicine Elmore.
A.V. Hadjinicolaou is funded by a NIHR/University of Cambridge Academic Clinical Lectureship.
A.V. Hadjinicolaou is funded by a Starter Grant from the Academy of Medical Sciences.
M. Tischkowitz was supported by the NIHR Cambridge Biomedical Research Centre.
This research received infrastructure support from the Experimental Cancer Medicine Centre and the National Institute for Health and Care Research (NIHR) Cambridge Biomedical Research Centre.

Abstract
Background
Prophylactic total gastrectomy is the definitive treatment for hereditary diffuse gastric cancer syndrome (HDGC). Endoscopic surveillance informs the requirement for and optimal timing of surgery. However, endoscopic recognition of early signet ring cell carcinoma (SRCC) remains challenging. We developed an endoscopic framework to optimize SRCC assessment during HDGC surveillance.
Methods
We retrospectively analyzed data from 147 individuals with HDGC undergoing endoscopic surveillance to evaluate the diagnostic accuracy of the endoscopic Cambridge criteria. We used machine learning to develop a clinical decision tree (cDT) to guide the application of the Cambridge criteria. We then prospectively validated the cDT in 66 CDH1 pathogenic-variant carriers. The interobserver agreement and diagnostic accuracy of the Cambridge criteria and cDT were assessed through a multi-reader multi-case study.
Results
Retrospective analysis of 537 endoscopies showed that the Cambridge criteria achieved 82.8% (48/58) sensitivity and 78.2% (140/179) specificity for SRCC diagnosis. The presence and number of neoplastic pale areas were independent predictors of higher cancer burden in HDGC individuals. In the prospective study, cDT had 77.8% (21/27) sensitivity and 90.7% (49/54) specificity, and improved performance of both experts and non-experts.
Conclusion
We developed and validated a practical endoscopic framework for enhancing SRCC assessment during HDGC endoscopic surveillance.
Publication History
Received: 17 February 2025
Accepted after revision: 12 June 2025
Accepted Manuscript online:
12 June 2025
Article published online:
30 July 2025
© 2025. Thieme. All rights reserved.
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
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