Simultaneous detection of circulating and disseminated tumor cells in primary breast cancer patients following neoadjuvant chemotherapy
Autor: | Andreas D. Hartkopf, Florin-Andrei Taran, Sara Y. Brucker, Vincent P. Walter, Markus Hahn, Markus Wallwiener |
---|---|
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Oncology medicine.medical_specialty Neoplasm Residual medicine.medical_treatment Breast Neoplasms 03 medical and health sciences Cytokeratin 0302 clinical medicine Circulating tumor cell Breast cancer Internal medicine medicine Humans Prospective Studies Neoplasm Metastasis Prospective cohort study Neoadjuvant therapy Chemotherapy Reverse Transcriptase Polymerase Chain Reaction business.industry Obstetrics and Gynecology General Medicine Middle Aged Neoplastic Cells Circulating Prognosis medicine.disease Immunohistochemistry Minimal residual disease Primary tumor Neoadjuvant Therapy 030104 developmental biology 030220 oncology & carcinogenesis Female business |
Zdroj: | Archives of Gynecology and Obstetrics. 297:785-790 |
ISSN: | 1432-0711 0932-0067 |
DOI: | 10.1007/s00404-018-4669-9 |
Popis: | Pathological complete response (pCR) is a common endpoint in neoadjuvant chemotherapy (NACT) of primary breast cancer patients (PBC), but does not address the systemic prevalence of minimal residual disease. In this study, we compared pCR with the detection of circulating (CTC) and disseminated tumor cells (DTC) following NACT, as well as their impact on survival. Patients with PBC receiving NACT and consecutive surgery were eligible for this study. CTCs were detected using the CellSearch® system and DTCs were determined using immunocytochemistry (cytokeratin staining with the A45-B/B3 antibody). pCR was defined as ypT0/ypTis and ypN0. 58 patients were included in the analysis with a median follow-up of 30 months. Of these, 5 (9%) presented with CTCs and 36 (62%) with DTCs. 16 patients (28%) achieved a pCR. No significant correlation between CTCs, DTCs and pCR and no statistically significant impact on disease free (DFS) or overall survival (OS) was apparent. Both CTCs and DTCs are detectable after NACT. As we could not show a significant relationship between CTC detection, DTC detection and pCR, all three methods may provide independent information regarding treatment response. Since we were unable to show a significant impact on survival, larger prospective studies that include CTCs and DTCs are needed. These trials should include the molecular characterization of primary tumor tissue, CTCs and DTCs to determine whether these cells are independent subpopulations of malignant cell clones. |
Databáze: | OpenAIRE |
Externí odkaz: |