Accelerating Cancer Histopathology Workflows with Chemical Imaging and Machine Learning

Author:

Falahkheirkhah Kianoush12ORCID,Mukherjee Sudipta S.1ORCID,Gupta Sounak3ORCID,Herrera-Hernandez Loren3ORCID,McCarthy Michael R.3ORCID,Jimenez Rafael E.3ORCID,Cheville John C.3ORCID,Bhargava Rohit124567ORCID

Affiliation:

1. 1Beckman Institute for Advanced Science and Technology, University of Illinois Urbana-Champaign, Urbana, Illinois.

2. 2Department of Bioengineering, University of Illinois Urbana-Champaign, Urbana, Illinois.

3. 3Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.

4. 4Department of Chemical and Biomolecular Engineering, University of Illinois Urbana-Champaign, Urbana, Illinois.

5. 5Department of Electrical and Computer Engineering, University of Illinois Urbana-Champaign, Urbana, Illinois.

6. 6Mechanical Science and Engineering, University of Illinois Urbana-Champaign, Urbana, Illinois.

7. 7Cancer Center at Illinois, University of Illinois Urbana-Champaign, Urbana, Illinois.

Abstract

Histopathology has remained a cornerstone for biomedical tissue assessment for over a century, with a resource-intensive workflow involving biopsy or excision, gross examination, sampling, tissue processing to snap frozen or formalin-fixed paraffin-embedded blocks, sectioning, staining, optical imaging, and microscopic assessment. Emerging chemical imaging approaches, including stimulated Raman scattering (SRS) microscopy, can directly measure inherent molecular composition in tissue (thereby dispensing with the need for tissue processing, sectioning, and using dyes) and can use artificial intelligence (AI) algorithms to provide high-quality images. Here we show the integration of SRS microscopy in a pathology workflow to rapidly record chemical information from minimally processed fresh-frozen prostate tissue. Instead of using thin sections, we record data from intact thick tissues and use optical sectioning to generate images from multiple planes. We use a deep learning–based processing pipeline to generate virtual hematoxylin and eosin images. Next, we extend the computational method to generate archival-quality images in minutes, which are equivalent to those obtained from hours/days-long formalin-fixed, paraffin-embedded processing. We assessed the quality of images from the perspective of enabling pathologists to make decisions, demonstrating that the virtual stained image quality was diagnostically useful and the interpathologist agreement on prostate cancer grade was not impacted. Finally, because this method does not wash away lipids and small molecules, we assessed the utility of lipid chemical composition in determining grade. Together, the combination of chemical imaging and AI provides novel capabilities for rapid assessments in pathology by reducing the complexity and burden of current workflows. Significance: Archival-quality (formalin-fixed paraffin-embedded), thin-section diagnostic images are obtained from thick-cut, fresh-frozen prostate tissues without dyes or stains to expedite cancer histopathology by combining SRS microscopy and machine learning.

Funder

HHS | NIH | National Cancer Institute

HHS | NIH | National Institute of Biomedical Imaging and Bioengineering

Cancer Center at Illinois

Publisher

American Association for Cancer Research (AACR)

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