Circulating tumor cell parameters during systemic therapy in primary breast cancer
https://doi.org/10.21294/1814-4861-2026-25-2-67-79
Abstract
Circulating tumor cells (CTCs) are frequently studied in terms of their prognostic significance during perioperative systemic therapy (periST) for breast cancer (BC). it is not yet clear whether there are unique changes in the CTC parameters that could be used as a predictor of the effectiveness of neoadjuvant (neoST) or adjuvant (aST) systemic therapy.
The aim of the study was a comparative analysis of parameters of once-isolated CTCs in BC patients with high risk of progression, who received neoST or aST.
Material and Methods. The study included BC 39 patients who received neo-ST (group 1: 16 patients) or aST (group 2: 23 patients). Blood sampling for CTC isolation using microfiltration was performed after 2–5 cycles of periST.
Results. No significant differences in the number of CTC-positive patients (87.5 % in group1 and 82.6 % in group 2) and the frequency of isolation of 5 or more CTCs (37.5 % in group 1 and 52.2 % in group 2, p=0.563), as well as CTC clusters (56.2 % and 43.5 % of patients in groups 1 and 2 groups, respectively, p=0.646) between the neoST and aST groups were found. There were no significant differences in the quantitative parameters (Me) of CTCs between the groups (1 group – 3 [1.8; 7.8] CTCs, 2 group – 5 [2; 6.5] CTCs, p=0.785). Regardless of the group, most patients had CTC clusters consisting of 2 to 3 cells (88.9 % and 100 % of patients in groups 1 and 2, respectively). During peri ST, a high count of CTCs was associated with the detection of CTC clusters and the presence of lymphatic metastases.
Conclusion. No significant differences in CTC count and characteristics between the neoST and aST groups were found. it indicates that breast tumor resection has a minor effect on CTC parameters. . The findings highlight that CTCs hold similar prognostic value regardless of whether they are measured before or after surgery, aiding in the prediction of periST.
Keywords
About the Authors
I. V. MikhailovRussian Federation
Ilya V. Mikhailov - MD, PhD, Head of the Department of Antitumor Drug Therapy.
61/2, Shchepkina St., Moscow, 129110
I. V. Grebennik
Russian Federation
Ivan V. Grebennik - Intern-Researcher, Laboratory of Biophysics.
1, Samory Mashela St., Moscow, 117198
A. A. Glazkov
Russian Federation
Alexey A. Glazkov - MD, PhD, Senior Researcher, Laboratory of Medical and Physical Research
Author ID (Scopus): 57199329515
ResearcherID (WOS): R-7373-2016
61/2, Shchepkina St., Moscow, 129110
I. A. Kruglova
Russian Federation
Irina A. Kruglova – MD.
47, Respublikanskaya St., Nizhny Novgorod, 603089
S. A. Kuznetsova
Russian Federation
Sofya A. Kuznetsova - PhD, Leading Researcher, Laboratory of Biophysics, D. Rogachev NRCPH, OI, Ministry of Health of Russia; Senior Researcher, Centre for Theoretical Problems of Physicochemical Pharmacology of the RAS
ResearcherID (WOS): N-1383-2014
1, Samory Mashela St., Moscow, 117198; 30, Srednyaya Kalitnikovskaya St., Moscow, 109029
A. S. Balkanov
Russian Federation
Andrey S. Balkanov - MD, DSc, Head of Radiotherapy Department
Author ID (Scopus): 6508333085
61/2, Shchepkina St., Moscow, 129110
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Supplementary files
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1. Fig. 1. Microphoto. Сirculating tumor cells (CTCs) in the blood of BC patients: a) a single СТС with an eccentrically located hyperchromatic nucleus with irregular (folded) contours; b) a homotypic СТС cluster; c) a heterotypic СТС cluster (including neutrophils). Pappenheim staining, ×1000. The size bar corresponds to 15 μm. Note: created by the authors | |
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2. Fig. 2. Microphoto. Circulating tumor cells in the blood of BC patients: a) Pappenheim staining, b) immunocytochemical staining for EpCAM (total light brown staining of the cytoplasm). ×1000. The size bar corresponds to 15 μm. Note: created by the authors | |
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| Type | Исследовательские инструменты | |
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Review
For citations:
Mikhailov I.V., Grebennik I.V., Glazkov A.A., Kruglova I.A., Kuznetsova S.A., Balkanov A.S. Circulating tumor cell parameters during systemic therapy in primary breast cancer. Siberian journal of oncology. 2026;25(2):67-79. (In Russ.) https://doi.org/10.21294/1814-4861-2026-25-2-67-79
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