What is it about?
This study explores whether micro‑Raman spectroscopy—a rapid, label‑free vibrational technique—can identify biochemical differences in the blood serum of patients with Chronic Lymphocytic Leukemia (CLL) and distinguish favorable from unfavorable prognostic categories. Serum samples from clinically classified CLL patients were analyzed, and their Raman spectra were processed using multivariate statistical methods, including Principal Component Analysis and Partial Least Squares. Specific spectral bands—such as those at 1652 and 1205 cm⁻¹, associated with protein conformation and amino acid composition, and the ratio between the 1003 cm⁻¹ (phenylalanine) and 1344 cm⁻¹ (collagen) peaks—were found to reflect metabolic variations correlated with prognosis
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Why is it important?
Traditional tools for CLL prognosis, such as morphology and immunophenotyping, provide only partial information. Raman spectroscopy offers a complementary and non‑destructive way to capture subtle biochemical changes in serum that may be linked to disease progression. Identifying a spectral “fingerprint” associated with prognosis could support earlier and more refined stratification of patients and offer new insights into the metabolic alterations underlying different disease trajectories.
Perspectives
These findings support the potential of Raman spectroscopy as an innovative adjunct tool for prognostic evaluation in CLL. Future work could expand sample size, validate spectral biomarkers across independent cohorts, and refine multivariate models to improve robustness. Integrating Raman‑based biochemical profiling with established molecular markers may help advance precision‑oriented stratification of CLL patients.
Prof. Antonio Speciale
University of Messina
Read the Original
This page is a summary of: Biochemical fingerprinting of dried blood serum from chronic lymphocytic leukemia patients by Raman spectroscopy: Towards prognostic classification, Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy, February 2026, Elsevier,
DOI: 10.1016/j.saa.2025.126961.
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