New method for real-time visualization and quantitative characterization of early colorectal cancer in endoscopy: a pilot study

Author:

Wagner Andrej1,Zandanell Stephan1,Ziachehabi Alexander2,Mitrakov Alexander3,Klieser Eckhard4,Neureiter Daniel4,Kiesslich Tobias15,Mayr Christian5,Berr Frieder1,Fedoruk Michael6,Singhartinger Franz7,Holzinger Josef7

Affiliation:

1. Department of Internal Medicine I, University Clinics Salzburg, Paracelsus Medical University, Salzburg, Austria

2. Department of Medicine II, Kepler Medical University, Linz, Austria

3. Endoscopy Division, Nizhniy Novgorod Cancer Hospital, Nizhniy Novgorod, Russian Federation

4. Institute of Pathology, Paracelsus Medical University/Salzburger Landeskliniken (SALK), Salzburg, Austria

5. Laboratory for Tumour Biology and Experimental Therapies (TREAT), Institute of Physiology and Pathophysiology, Paracelsus Medical University, Salzburg, Austria

6. Vortex Photonics, Planegg, Germany

7. Department of Surgery, University Clinics Salzburg, Paracelsus Medical University, Salzburg, Austria

Abstract

Abstract Background and study aims Endoscopic optical diagnosis is crucial to the therapeutic strategy for early gastrointestinal cancer. It accurately (> 85 %) predicts pT category based on microsurface (SP) and vascular patterns (VP). However, interobserver variability is a major problem. We have visualized and digitalized the graded irregularities based on bioinformatically enhanced quantitative endoscopic image analysis (BEE) of high-definition white-light images. Methods In a pilot study of 26 large colorectal lesions (LCLs, mean diameter 39 mm), we retrospectively compared BEE variables with corresponding histopathology of the resected LCLs. Results We included 10 adenomas with low-grade intraepithelial neoplasia (LGIN), nine with high-grade intraepithelial neoplasia (HGIN) and early adenocarcinoma (EAC), and seven deeply submucosal invasive carcinomas. Quantified density (d) and nonuniformity (CU) of vascular and surface structures correlated with histology (rs d VP: –0.77, rs CU VP: 0.13, rs d SP: –0.76, and rs CU SP: 0.45, respectively). A computed BEE score showed a sensitivity and specificity of 90 % and 100 % in the group with LGINs, 89 % and 41 % in the group with HGINs and EACs, and 100 % and 95 % in the group with deeply invasive carcinoma, respectively. Conclusions In this pilot study, BEE showed promise as a tool for endoscopic characterization of LCLs during routine endoscopy. Prospective clinical studies are needed.

Publisher

Georg Thieme Verlag KG

Subject

Gastroenterology,Medicine (miscellaneous)

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