Endoscopy
DOI: 10.1055/a-2634-7895
Innovations and brief communications

Clinical decision tree for optimizing endoscopic assessment of signet ring cell carcinoma in hereditary diffuse gastric cancer surveillance

Lianlian Wu
1   Early Cancer Institute, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom of Great Britain and Northern Ireland
2   Renmin Hospital of Wuhan University, Wuhan University, Wuhan, China
,
Judith Honing
1   Early Cancer Institute, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom of Great Britain and Northern Ireland
3   Department of Gastroenterology and Hepatology, Rotterdam Medical Centre, University Medical Centre Rotterdam, Rotterdam, Netherlands
,
Anjui Wu
1   Early Cancer Institute, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Sonia S. Kupfer
4   Section of Gastroenterology, Hepatology and Nutrition, University of Chicago, Chicago, United States
,
Tanya M. Bisseling
5   Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, Netherlands
,
Jolanda M. van Dieren
6   Department of Gastrointestinal Oncology, The Netherlands Cancer Institute, Amsterdam, Netherlands
,
W. Keith Tan
1   Early Cancer Institute, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Colin Y. C. Lee
1   Early Cancer Institute, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Andreas V. Hadjinicolaou
1   Early Cancer Institute, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom of Great Britain and Northern Ireland
7   Department of Gastroenterology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Yuan Huang
8   Department of Applied Mathematics and Theoretical Physics, University of Cambridge, Cambridge, United Kingdom of Great Britain and Northern Ireland
9   Department of Medicine, University of Cambridge, Cambridge, United Kingdom of Great Britain and Northern Ireland (Ringgold ID: RIN2152)
,
Juan de la Revilla Negro
7   Department of Gastroenterology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Mohmmed Tauseef Sharip
7   Department of Gastroenterology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Joshua Elias
7   Department of Gastroenterology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Hui Jun Lim
1   Early Cancer Institute, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Nandini Karthik
1   Early Cancer Institute, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Greta Markert
10   Cancer Research UK Cambridge Institute, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
William Prew
10   Cancer Research UK Cambridge Institute, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Maria O’Donovan
11   Department of Histopathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom of Great Britain and Northern Ireland (Ringgold ID: RIN2153)
,
Marc Tischkowitz
12   Department of Medical Genetics, National Institute for Health Research, Cambridge Biomedical Research Centre, University of Cambridge, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Vijayendran Sujendran
13   Cambridge Oesophagus-gastric Centre, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom of Great Britain and Northern Ireland (Ringgold ID: RIN2153)
,
J. Robert O'Neill
1   Early Cancer Institute, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom of Great Britain and Northern Ireland
14   Cambridge Oesophagus-Gastric Centre, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom of Great Britain and Northern Ireland
15   Edinburgh Cancer Research, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom of Great Britain and Northern Ireland
,
Florian Markowetz
16   Cancer Research UK Cambridge Research Institute, Cambridge, United Kingdom of Great Britain and Northern Ireland (Ringgold ID: RIN92690)
,
Rebecca C. Fitzgerald
1   Early Cancer Institute, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom of Great Britain and Northern Ireland
,
Massimiliano di Pietro
1   Early Cancer Institute, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom of Great Britain and Northern Ireland
› Author Affiliations

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.


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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.

Supplementary Material



Publication History

Received: 17 February 2025

Accepted after revision: 12 June 2025

Accepted Manuscript online:
12 June 2025

Article published online:
30 July 2025

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