Diagnostic potential of plasma CD30(+) small extracellular vesicles in Hodgkin lymphoma
- Authors: Katsuba K.E.1, Kramynin L.A.1, Slyusarenko M.A.1, Shalaev A.V.1, Sharoyko V.V.2, Valitova A.A.1, Artem’eva A.S.1, Krzhivitskiy P.I.1, Filatova L.V.1, Malek A.V.1
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Affiliations:
- N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of Russia
- I.P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia
- Issue: Vol 18, No 4 (2023)
- Pages: 145-155
- Section: NEW DIRECTIONS, DIAGNOSTIC OPPORTUNITIES, AND TREATMENT ADVANCES
- Published: 08.12.2023
- URL: https://oncohematology.abvpress.ru/ongm/article/view/875
- DOI: https://doi.org/10.17650/1818-8346-2023-18-4-145-155
- ID: 875
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Abstract
Background. In current clinical practice, there are no reliable methods to stratify patients with a high risk of relapse or with a primary refractory form of Hodgkin lymphoma. Quantification of CD30-positive small extracellular vesicles (CD30(+)SEV) in plasma seems to be a possible approach to solve this issue. CD30(+)SEV can be quantified by the AuNP aptasensor technology based on the enzyme-mimetic properties of gold nanoparticles and the CD30-specific affinity of DNA aptamers.
Aim. To quantify CD30(+)SEV in the plasma of patients with newly diagnosed Hodgkin lymphoma; to investigate the links between estimated parameter and clinical/morphological properties of disease and the effect of first two chemotherapy cycles.
Material and methods. A semi-quantitative analysis of CD30(+)SEV in the plasma of patients with Hodgkin lymphoma (n = 55) was performed using the AuNP aptasensor. The relationship between the CD30(+)SEV concentration and the data of standard diagnostic approaches was evaluated through the r-Pearson correlation coefficient, the Mann–Whitney and Kruskal–Wallis criteria.
Results. The plasma concentration of CD30(+)SEV in patients with Hodgkin lymphoma correlates with the quantity of CD30(+) cells in tissues of biopsied lymph nodes (r = 0.8) and the total lesion glycolysis estimated by PET/CT (r = 0.9). Patients with a relatively high concentration of CD30(+)SEV are characterized by an increase of erythrocyte sedimentation rate and leukocytosis compared with patients with a lower concentration of CD30(+)SEV. Two cycles of chemotherapy reduced CD30(+)SEV concentration, and this effect was more pronounced in patients treated with ABVD (doxorubicin, bleomycin, vinblastine, dacarbazine) regime than the BEACOPPesc (bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, prednisolone, procarbazine).
Conclusion. AuNP-aptasensor can be used for semi-quantitative assessment of CD30(+)SEV in plasma. The estimated CD30(+)SEV concentration correlates with the clinical and morphological parameters of patients with Hodgkin lymphoma and may reflect the severity of the disease. To assess the diagnostic and/or prognostic potential of developed technology, large-scale multicenter studies are required.
About the authors
K. E. Katsuba
N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of Russia
ORCID iD: 0000-0002-7373-5206
68 Leningradskaya St., Pesochnyy, Saint Petersburg 197758
Russian FederationL. A. Kramynin
N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of Russia
ORCID iD: 0000-0003-4542-8353
68 Leningradskaya St., Pesochnyy, Saint Petersburg 197758
Russian FederationM. A. Slyusarenko
N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of Russia
ORCID iD: 0000-0002-3677-1558
68 Leningradskaya St., Pesochnyy, Saint Petersburg 197758
Russian FederationA. V. Shalaev
N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of Russia
ORCID iD: 0000-0002-6148-6994
68 Leningradskaya St., Pesochnyy, Saint Petersburg 197758
Russian FederationV. V. Sharoyko
I.P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia
ORCID iD: 0000-0002-3717-0471
6–8 L’va Tolstogo St., Saint Petersburg 197022
Russian FederationA. A. Valitova
N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of Russia
ORCID iD: 0000-0002-1279-4667
68 Leningradskaya St., Pesochnyy, Saint Petersburg 197758
Russian FederationA. S. Artem’eva
N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of Russia
ORCID iD: 0000-0002-2948-397X
68 Leningradskaya St., Pesochnyy, Saint Petersburg 197758
Russian FederationP. I. Krzhivitskiy
N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of Russia
ORCID iD: 0000-0002-6864-6348
68 Leningradskaya St., Pesochnyy, Saint Petersburg 197758
Russian FederationL. V. Filatova
N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of Russia
ORCID iD: 0000-0002-0728-4582
68 Leningradskaya St., Pesochnyy, Saint Petersburg 197758
Russian FederationA. V. Malek
N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of Russia
Author for correspondence.
Email: anastasia@malek.com.ru
ORCID iD: 0000-0001-5334-7292
Anastasiya V. Malek
68 Leningradskaya St., Pesochnyy, Saint Petersburg 197758
Russian FederationReferences
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