Abstract

.Significance: The early detection of dysplasia in patients with Barrett’s esophagus could improve outcomes by enabling curative intervention; however, dysplasia is often inconspicuous using conventional white-light endoscopy.Aim: We sought to determine whether multispectral imaging (MSI) could be applied in endoscopy to improve detection of dysplasia in the upper gastrointestinal (GI) tract.Approach: We used a commercial fiberscope to relay imaging data from within the upper GI tract to a snapshot MSI camera capable of collecting data from nine spectral bands. The system was deployed in a pilot clinical study of 20 patients (ClinicalTrials.gov NCT03388047) to capture 727 in vivo image cubes matched with gold-standard diagnosis from histopathology. We compared the performance of seven learning-based methods for data classification, including linear discriminant analysis, -nearest neighbor classification, and a neural network.Results: Validation of our approach using a Macbeth color chart achieved an image-based classification accuracy of 96.5%. Although our patient cohort showed significant intra- and interpatient variance, we were able to resolve disease-specific contributions to the recorded MSI data. In classification, a combined principal component analysis and -nearest-neighbor approach performed best, achieving accuracies of 95.8%, 90.7%, and 76.1%, respectively, for squamous, non-dysplastic Barrett’s esophagus and neoplasia based on majority decisions per-image.Conclusions: MSI shows promise for disease classification in Barrett’s esophagus and merits further investigation as a tool in high-definition “chip-on-tip” endoscopes.

Highlights

  • Patients with Barrett’s esophagus[1] (BE) undergo routine surveillance using high-resolution white light endoscopy (HR-WLE) and random biopsies to detect the presence of dysplasia, which increases the risk of developing esophageal adenocarcinoma.[2]

  • We have previously shown that Spectrally resolved detector arrays (SRDAs) can be implemented in combination with such an imaging-fiber bundle without reducing resolution, since the resolution of fiberscope-based imaging is limited by the size of individual fiberlets rather than by the sensor resolution.[45]

  • The multispectral endoscope was deployed to acquire in vivo esophageal image cubes

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Summary

Introduction

Patients with Barrett’s esophagus[1] (BE) undergo routine surveillance using high-resolution white light endoscopy (HR-WLE) and random biopsies to detect the presence of dysplasia, which increases the risk of developing esophageal adenocarcinoma.[2] Early detection of the precursor dysplastic lesions, or early-stage cancer, enables curative intervention, increasing the 5-year survival rate from just 15%–25% to 80%.3–5. These precursor lesions can be challenging to identify on standard-of-care HR-WLE.[6,7]. Disease-related structural and biochemical changes in the epithelial layer of the gastrointestinal (GI) tract can alter the distribution and abundance of these absorbers and scatterers—for example, neovascularization increasing hemoglobin abundance in the epithelium11—resulting in subtle wavelength-dependent changes in reflected light, which can be measured by point-based spectroscopy methods[12] and by hyperspectral imaging methods that capture spatially resolved ðx; yÞ and spectral (wavelength, λ) information in a single data set, often using mechanical scanning.[13,14]

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