Method for identifying malignancies in barrett's esophagus using white light endoscopy

a barrett's esophagus and white light technology, applied in the field of white light endoscopy, can solve the problems of time-consuming, and achieve the effect of drastically reducing improving the discrimination between be and dysplasia

Inactive Publication Date: 2010-04-08
NOVADAG TECH INC
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Problems solved by technology

Recently developed methods are either small field of view and, consequently, very time consuming (Raman spectroscopy, Optical Coherence Tomography, Doppler Optical Coherence Tomography, Laser Scattering Spectroscopy, confocal endoscopy) or require application of external dyes (chromo-endoscopy, fluorescence imaging of ALA-5 staining) Narrow band imaging and near-infrared multimodal endoscopy methods were reported just within last two years and still required to prove its sensitivity and specificity abilities.

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  • Method for identifying malignancies in barrett's esophagus using white light endoscopy
  • Method for identifying malignancies in barrett's esophagus using white light endoscopy
  • Method for identifying malignancies in barrett's esophagus using white light endoscopy

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Embodiment Construction

[0014]An adjuvant screening technique is described which is compatible with conventional white light endoscopy to guide the biopsy collection in Barrett's esophagus (BE) in real time. By systematic analysis of the diffuse reflectance spectra, we have found a specific algorithm, that provides statistically-significant discrimination between BE and dysplasia, with or without the presence of an inflammatory component.

[0015]An understanding of the blood microcirculation in tumors is important for their detection, diagnosis and treatment. Relatively high values of blood supply in tumors are associated with increased metabolism and aggressiveness. Increase of blood supply provides a growing cancerous tissue with additional nutrients via growth of new vasculature through a mechanism called angiogenesis. Typical development of epithelial-originating cancers occurs in several sequential stages—low grade dysplasia or pre-cancer, high grade dysplasia, carcinoma in situ, invasive cancer, and fi...

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Abstract

A method is described for computing a statistically significant difference between dysplasia and Barrett's esophagus (both with and without inflammatory component) using a discriminate function with diffuse reflectance measurements performed at a minimum of four different wavelengths of 485, 513, 598, and 629 nm. The discriminate function found depends both on local blood fraction volume THB and oxygenation SO2. A pull-back approach of spectral data acquisition is disclosed which takes into account tissue motility in esophagus and measurement geometry peculiarities. The pull-back approach provides a significant improvement of measurement reproducibility and reduction of data deviation by 75-100%, resulting in a better discrimination between different histological groups.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application claims priority to U.S. Provisional Application Ser. No. 61 / 102,091, filed Oct. 2, 2008, the entire content of which is incorporated herein by reference.FIELD OF THE INVENTION[0002]The invention relates to white light endoscopy to guide the biopsy collection, and more particularly to detecting an intrinsic optical signature of early cancer lesions in Barrett's esophagus (BE) using diffuse reflectance spectroscopy, without staining or dying to enhance malignant / non-malignant contrast.BACKGROUND OF THE INVENTION[0003]Gastrointestinal (GI) malignancies continue to be the second leading cause of cancer-related deaths in the United States (24%). One of the highest shares in GI malignancies belongs to esophagus cancer (10% or 12000-14000 per year based on 2000-2003 statistics). People from the Western hemisphere tend to develop esophageal cancer based on prior metaplastic mucosal transformation often called as Barrett's esophag...

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61B6/00
CPCA61B1/043A61B5/0071A61B5/4233A61B5/0084A61B5/0075
Inventor DOUPLIK, ALEXANDREADLER, DESMOND C.WILSON, BRIAN C.MARCON, NORMAN
Owner NOVADAG TECH INC
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