Abstract
Modern photonic technologies are emerging, allowing the acquisition of in-vivo endoscopic tissue imaging at a microscopic scale, with characteristics comparable to traditional histological slides, and with a label-free modality. This raises the possibility of an ‘optical biopsy’ to aid clinical decision making. This approach faces barriers for being incorporated into clinical practice, including the lack of existing images for training, unfamiliarity of clinicians with the novel image domains and the uncertainty of trusting ‘black-box’ machine learned image analysis, where the decision making remains inscrutable. In this paper, we propose a new method to transform images from novel photonics techniques (e.g. autofluorescence microscopy) into already established domains such as Hematoxilyn-Eosin (H-E) microscopy through virtual reconstruction and staining. We introduce three main innovations: 1) we propose a transformation method based on a Siamese structure that simultaneously learns the direct and inverse transformation ensuring domain back-transformation quality of the transformed data. 2) We also introduced an embedding loss term that ensures similarity not only at pixel level, but also at the image embedding description level. This drastically reduces the perception distortion trade-off problem existing in common domain transfer based on generative adversarial networks. These virtually stained images can serve as reference standard images for comparison with the already known H-E images. 3) We also incorporate an uncertainty margin concept that allows the network to measure its own confidence, and demonstrate that these reconstructed and virtually stained images can be used on previously-studied classification models of H-E images that have been computationally degraded and de-stained. The three proposed methods can be seamlessly incorporated on any existing architectures. We obtained balanced accuracies of 0.95 and negative predictive values of 1.00 over the reconstructed and virtually stained image-set on the detection of color-rectal tumoral tissue. This is of great importance as we reduce the need for extensive labeled datasets for training, which are normally not available on the early studies of a new imaging technology.
Highlights
White light endoscopy and biopsy are performed respectively for clinical and histological assessment of the gastrointestinalThe associate editor coordinating the review of this manuscript and approving it for publication was Ali Shariq Imran .tract [1]
2) We introduced an embedding loss term that ensures similarity at pixel level, and at the image embedding description level
This drastically reduces the perception distortion trade-off problem existing in common domain transfer based on generative adversarial networks
Summary
Other studies have reported concerns on such a system providing just a ‘black-box’ prediction of lesion histology and expressed their desire to have the information to understand the diagnostic decision process [19], [20] Based on these studies, we summarize that optical biopsy models:. This cross-domain image translation eliminates the need for a large, varied and annotated dataset on the novel images to generate an inference model as optical biopsy can be performed over target domain models. We hypothesise that these cross-modal translated images (reconstructed and virtually stained) can be successfully used with existing cancer classification models trained with existing H-E images.
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