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Automatic subtyping of Diffuse Large B-cell Lymphomas (DLBCL): Raman-based genetic and metabolic classification
Patrycja Dawiec1, Patrycja Leszczenko1, Anna M Nowakowska2
1Department of Chemical Physics, Faculty of Chemistry, Jagiellonian University, Krakow, Poland; Doctoral School of Exact and Natural Sciences, Jagiellonian University, Krakow, Poland.
Summary
Raman imaging offers a new way to classify Diffuse Large B-cell Lymphoma (DLBCL) subtypes. This technique analyzes spectral profiles to identify DLBCL cells and their specific metabolic or cell-of-origin subtypes.
Area of Science:
- Biomedical Optics
- Molecular Spectroscopy
- Oncology
Background:
- Diffuse Large B-cell Lymphoma (DLBCL) is a common, aggressive blood cancer with significant heterogeneity.
- Accurate classification of DLBCL subtypes is crucial for effective treatment selection but remains challenging.
- Existing diagnostic methods struggle with the molecular complexity and metabolic variability of DLBCL.
Purpose of the Study:
- To evaluate Raman imaging as a diagnostic tool for classifying DLBCL cells.
- To develop and present models for automated DLBCL cell identification and subtype assignment.
- To correlate spectral profiles with biochemical, genetic, and metabolic features of DLBCL subtypes.
Main Methods:
- Utilized Raman imaging to acquire spectral data from DLBCL cells.
- Developed classification models based on Raman spectra for automated identification.
- Assigned DLBCL cells to cell-of-origin (COO) subtypes (ABC/GCB) and comprehensive cluster classification (CCC) subtypes (OxPhos/non-OxPhos).
Main Results:
- Raman imaging provides unique biochemical and metabolic information from DLBCL cells.
- Developed models successfully identified DLBCL cells and assigned them to specific subtypes.
- Distinct spectral profiles were identified for each lymphoma subtype, linked to underlying biological characteristics.
Conclusions:
- Raman imaging demonstrates high diagnostic potential for DLBCL classification.
- Automated spectral analysis enables efficient and accurate identification of DLBCL subtypes.
- This technique offers a novel approach to understanding DLBCL heterogeneity and guiding treatment.

