Abstract
The presence of circulating tumor cells in the blood of patients with triple negative breast cancer (early and locally advanced cancer) before and after preoperative chemotherapy was assessed using expression markers. Before therapy, circulating tumor cells were detected in 5 of 13 (38%) patients with early cancer and in 7 of 17 (41.2%) patients with locally advanced cancer. After therapy, the circulating immune cells were detected in one patient with locally advanced cancer, who had no circulating cells before therapy. The tumor was resistant to chemotherapy and the disease progressed. The detected circulating tumor cells were HER-2-positive, while the primary tumor was HER-2-negative. It was concluded that the circulating immune cells can be a potential marker of the efficiency of therapy and predictors of the disease course, while their phenotype can differ from the phenotype of the primary tumor.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Aged
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Antineoplastic Agents / therapeutic use
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Biomarkers, Tumor / genetics*
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Biomarkers, Tumor / metabolism
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Carcinoma in Situ / diagnosis*
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Carcinoma in Situ / drug therapy
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Carcinoma in Situ / genetics
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Carcinoma in Situ / pathology
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Carcinoma, Ductal, Breast / diagnosis*
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Carcinoma, Ductal, Breast / drug therapy
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Carcinoma, Ductal, Breast / genetics
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Carcinoma, Ductal, Breast / pathology
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Chemotherapy, Adjuvant
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Drug Resistance, Neoplasm
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Female
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Gene Expression
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Genotype
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Humans
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Middle Aged
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Neoplasm Recurrence, Local / diagnosis*
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Neoplasm Recurrence, Local / drug therapy
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Neoplasm Recurrence, Local / genetics
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Neoplasm Recurrence, Local / pathology
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Neoplastic Cells, Circulating / metabolism*
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Neoplastic Cells, Circulating / pathology
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Phenotype
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Prognosis
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Receptor, ErbB-2 / genetics
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Receptor, ErbB-2 / metabolism
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Receptors, Estrogen / genetics
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Receptors, Estrogen / metabolism
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Receptors, Progesterone / genetics
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Receptors, Progesterone / metabolism
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Triple Negative Breast Neoplasms / diagnosis*
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Triple Negative Breast Neoplasms / drug therapy
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Triple Negative Breast Neoplasms / genetics
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Triple Negative Breast Neoplasms / pathology
Substances
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Antineoplastic Agents
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Biomarkers, Tumor
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Receptors, Estrogen
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Receptors, Progesterone
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ERBB2 protein, human
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Receptor, ErbB-2