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New research · Gastroenterology
Gut · 2d
StudyGut · 2026

Risk-based pathology reporting after endoscopic submucosal dissection for early gastrointestinal cancer: international consensus standards.

Kareem Khalaf, Huaqi Li, Mai Iwaya … Robert Bechara
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GastroenterologyStudy

International experts developed 56 consensus recommendations for ESD pathology reporting.

Risk-based pathology reporting after endoscopic submucosal dissection for early gastrointestinal cancer: international consensus standards.

Kareem Khalaf et al. · Gut · 2026
Background

Endoscopic submucosal dissection (ESD) enables en bloc resection of early gastrointestinal cancers and provides specimens suitable for precise pathological risk assessment.

Purpose

To develop practical international standards for pathology assessment and reporting of invasive carcinoma in ESD specimens.

Methods

An international panel of 42 experts, including 28 gastrointestinal pathologists and 14 therapeutic endoscopists from 15 countries, participated in a modified Delphi consensus process.

n = 42 experts
56
Results
recommendations
international experts agreed on guidelines for reporting findings from early cancer samples
n = 42 experts
More results

The panel recommends using Sm1-Sm3 subclassification only when the muscularis propria is present; otherwise, submucosal invasion depth should be reported in micrometres, rounded to the nearest 100 µm.

Submucosal invasion breadth should be reported in millimetres as an adjunct metric for future validation.

More results

Tumour budding should be reported according to International Tumour Budding Consensus Conference criteria, and differentiation, histological subtype, lymphovascular invasion, perineural invasion and margin status should be integrated into composite risk assessment.

“
Conclusion · 1 of 2

These consensus standards provide immediately implementable, synoptic-ready pathology reporting criteria after ESD.

Conclusion · 2 of 2

By standardising measurement landmarks, margin terminology, ancillary stain use and reporting of adverse histological features, they aim to reduce interinstitutional variability, improve multidisciplinary decision-making and support future validation of risk models in early gastrointestinal cancer.

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