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Clinical Trials/NCT01048918
NCT01048918
Completed
Not Applicable

Characterization of Circulating Tumor Cells (CTC-s) in Patients With Locally Advanced or Metastatic Stage IV Breast Cancer

City of Hope Medical Center1 site in 1 country280 target enrollmentSeptember 4, 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Locally Advanced Breast Cancer
Sponsor
City of Hope Medical Center
Enrollment
280
Locations
1
Primary Endpoint
Targets ER, Her2, and possible M30, VEGFR2, EGFR. Tumor cells found in blood stream.
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to identify tumor cells in the bloodstream (Circulating Tumor Cells, CTC's) from patient's with locally advanced or metastatic (stage IV) breast cancer. Analyzing the tumor is helpful in guiding therapy; however, research has suggested that the number of tumor cells found in the bloodstream (CTC's) signifies more aggressive behavior and increased difficulty in eliminating the cancer. This research will help to develop better ways to treat breast cancer which could be tailored to a patient and may be adjusted to a patient's individual needs.

Detailed Description

Up to 60 mL of blood will be collected from each patient at up to 6 time points. Samples will be delivered to the Bruce Laboratory (Palo Alto Research Center) for immunolabeling and FAST scanning. The FAST scanning will utilize CK+, CD45-and DAPI+ labeling as well as cell morphology confirmed by collaborating pathologists to select for CTC with the technology allowing for assessment of up to four additional protein expressions on the surface of CTC's. Additional samples at the proposed time points will be placed on ice and sent over to the Wang Laboratory for the purpose of extracting RNA/microRNA and proteins from CTC's for profiling and further analysis. Benefits are only to society, not the individual. Knowledge obtained from applying the two technologies may help with better selection of therapy, early detection of progression, possibly better diagnosis and development of targeted therapeutic agents in the future.

Registry
clinicaltrials.gov
Start Date
September 4, 2008
End Date
April 8, 2022
Last Updated
2 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
City of Hope Medical Center
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients must be \> 18 years old.
  • Patients are being treated for breast cancer at City of Hope (COH).

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Targets ER, Her2, and possible M30, VEGFR2, EGFR. Tumor cells found in blood stream.

Time Frame: Blood will be collected at up to 6 time points: Prior to initiating therapy, 8-12 weeks, 20-24 weeks, and at 9,12 and 24 months after initiation of therapy.

Secondary Outcomes

  • Banking leftover blood. Used for future research purposes that have not yet been determined.(Future)

Study Sites (1)

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