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Noninvasive virtual biopsy using micro-registered optical coherence tomography (OCT) in human subjects
Yonatan Winetraub1,2,3,4, Aidan Van Vleck1, Edwin Yuan1,2,5
1Department of Structural Biology, Stanford University, Stanford, CA 94305, USA.
Science Advances
|April 10, 2024
Summary
Researchers developed a novel method to virtually stain intact tissue images, converting noninvasive optical coherence tomography (OCT) scans into detailed hematoxylin and eosin (H&E) slides. This innovation aims to reduce the need for invasive biopsy procedures in cancer diagnosis.
Area of Science:
- Biomedical Imaging
- Computational Pathology
- Medical Diagnostics
Background:
- Histological hematoxylin and eosin (H&E) staining is the gold standard for cancer diagnosis but is invasive and time-consuming.
- Virtual staining of unstained slides shows promise, but true virtual biopsy requires imaging intact tissue.
Purpose of the Study:
- To develop a method for virtual H&E staining of intact tissue using noninvasive imaging.
- To enable high-fidelity conversion of optical coherence tomography (OCT) images to H&E-like images for pathology.
Main Methods:
- Developed a micron-accuracy coregistration technique to align 2D H&E slides with 3D OCT images of the same tissue.
- Trained a conditional generative adversarial network (cGAN) on paired H&E and OCT datasets.
- Applied the cGAN to convert noninvasive OCT images into virtually stained H&E slices in 2D and 3D.
Main Results:
- Achieved high-fidelity virtual H&E staining from noninvasive OCT images.
- Demonstrated successful 2D and 3D virtual staining of tissue sections.
- Validated the coregistration and virtual staining method on fresh tissue samples.
Conclusions:
- The developed method enables virtual biopsy by converting OCT images to H&E slices.
- This approach has the potential to reduce the number of invasive biopsy procedures.
- Facilitates the clinical integration of OCT imaging for disease diagnosis and margin assessment.

