Frontiers in Oncology (Mar 2023)

Towards targeted colorectal cancer biopsy based on tissue morphology assessment by compression optical coherence elastography

  • Anton A. Plekhanov,
  • Marina A. Sirotkina,
  • Ekaterina V. Gubarkova,
  • Elena B. Kiseleva,
  • Alexander A. Sovetsky,
  • Maria M. Karabut,
  • Vladimir E. Zagainov,
  • Vladimir E. Zagainov,
  • Sergey S. Kuznetsov,
  • Anna V. Maslennikova,
  • Elena V. Zagaynova,
  • Elena V. Zagaynova,
  • Vladimir Y. Zaitsev,
  • Natalia D. Gladkova

DOI
https://doi.org/10.3389/fonc.2023.1121838
Journal volume & issue
Vol. 13

Abstract

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Identifying the precise topography of cancer for targeted biopsy in colonoscopic examination is a challenge in current diagnostic practice. For the first time we demonstrate the use of compression optical coherence elastography (C-OCE) technology as a new functional OCT modality for differentiating between cancerous and non-cancerous tissues in colon and detecting their morphological features on the basis of measurement of tissue elastic properties. The method uses pre-determined stiffness values (Young’s modulus) to distinguish between different morphological structures of normal (mucosa and submucosa), benign tumor (adenoma) and malignant tumor tissue (including cancer cells, gland-like structures, cribriform gland-like structures, stromal fibers, extracellular mucin). After analyzing in excess of fifty tissue samples, a threshold stiffness value of 520 kPa was suggested above which areas of colorectal cancer were detected invariably. A high Pearson correlation (r =0.98; p <0.05), and a negligible bias (0.22) by good agreement of the segmentation results of C-OCE and histological (reference standard) images was demonstrated, indicating the efficiency of C-OCE to identify the precise localization of colorectal cancer and the possibility to perform targeted biopsy. Furthermore, we demonstrated the ability of C-OCE to differentiate morphological subtypes of colorectal cancer – low-grade and high-grade colorectal adenocarcinomas, mucinous adenocarcinoma, and cribriform patterns. The obtained ex vivo results highlight prospects of C-OCE for high-level colon malignancy detection. The future endoscopic use of C-OCE will allow targeted biopsy sampling and simultaneous rapid analysis of the heterogeneous morphology of colon tumors.

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