Circulating Tumor Cells as Predictors of Response and Failure in Breast Cancer Patients Treated with Preoperative Chemotherapy

Author:

Boutrus Rimoun R.1,Raad Rita F. Abi1,Kuter Irene2,Ancukiewicz Marek1,Roberts Lisa3,Solomon Natalie3,Ngo Taylor4,Borick Heather4,Ryan Paula2,Moy Beverly2,Gadd Michele5,Chien Jo6,Younger Jerry2,Smith Barbara5,Taghian Alphonse G.1,Harris Lyndsay7

Affiliation:

1. Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston - USA

2. Department of Medicine, Hematology-Oncology Unit, Massachusetts General Hospital, Harvard Medical School, Boston - USA

3. Abbott Molecular Inc., Des Plaines, Illinois - USA

4. Department of Cancer Biology/Adult Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston - USA

5. Department of Surgery, Division of Surgical Oncology, Massachusetts General Hospital, Harvard Medical School, Boston - USA

6. Department of Medicine, Division of Hematology-Oncology, University of California San Francisco, San Francisco - USA

7. Breast Cancer Program, Section of Medical Oncology, Yale Cancer Center, Yale University School of Medicine, New Haven - USA

Abstract

Aim To explore the significance of circulating tumor cells (CTCs) detection in the course of preoperative chemotherapy (PC) and their effect on the outcomes. Methods Fifty-five patients with stage II/III invasive breast cancer were enrolled into a preoperative clinical trial. Patients were given PC with sequential single-agent doxorubicin and paclitaxel vs paclitaxel followed by doxorubicin. Blood samples (8 mL) were collected from patients before PC, after each phase, and at 6 months intervals during follow-up. Peripheral blood mononuclear cells were isolated and enriched for epithelial cells. Quantitative RT-PCR was used to determine the presence of cytokeratin 19 (CK19) mRNA. Samples were considered positive when the PCR curve crossed the standard threshold curve. Results After the first phase of chemotherapy, there was a 59% overall reduction in the median tumor volume. The percentage of volume reduction did not differ between patients who presented with detectable CTCs at baseline and those who did not (p=0.89). After the second phase of chemotherapy, there was a further decrease in the median tumor volume to 93% from baseline. There was no correlation between the lack of response and the presence of CTCs either after the first (p=0.36) or second (p=0.5391) phases of PC. The presence of CTCs was a predictor of local or distant relapse (p=0.0411). The detection of CTCs did not affect overall survival (p=0.2569). Conclusion CTCs can be used as predictors of relapse after definitive treatment of locally advanced breast cancer; however, CTCs detection in peripheral blood during the course of PC does not implicate a particular pattern of response to treatment.

Publisher

SAGE Publications

Subject

Cancer Research,Clinical Biochemistry,Oncology,Pathology and Forensic Medicine

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