Breast Cancer Clinical Trial

Determine Feasibility of Quantifying Apoptosis and Bcl-2 Expression in CTCs in Women With Metastatic Breast Cancer

Summary

We are trying to develop better ways to detect when cancer therapies are working.

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Eligibility Criteria

Inclusion Criteria:

1.Females at least 18 years of age 2 Diagnosis of metastatic breast cancer 3.ECOG Score of 0-2 4.Treating oncologist has decided to initiate any new systemic therapy with emphasis on recruiting patients commencing a taxane-based regimen. Taxine-based therapy may be docetaxel or paclitaxel, and it can be given on any schedule,including weekly or every 3 weeks. Other treatment can include non-taxane chemotherapy or trastuzumab-with or without other therapy.

5.Patient is willing to return for one or more additional ~18 mL blood draw (s) at 24-48-, and /or 72 hours and ~3-4 weeks after the initiation of therapy.At a minimum, patients must donate blood at baseline, one intermediate interval (24, 48, 72 hr) and at ~3-4 weeks 6.Signed Informed Consent Form

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Exclusion Criteria:

Patient is unable and unwilling to provide a blood specimen at a minimum of one of the intermediate blood draw time points at 24, 48, or 72 hours -

Study is for people with:

Breast Cancer

Estimated Enrollment:

69

Study ID:

NCT00156273

Recruitment Status:

Completed

Sponsor:

University of Michigan Rogel Cancer Center

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There is 1 Location for this study

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University of Michigan Cancer Center
Ann Arbor Michigan, 48109, United States

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Study is for people with:

Breast Cancer

Estimated Enrollment:

69

Study ID:

NCT00156273

Recruitment Status:

Completed

Sponsor:


University of Michigan Rogel Cancer Center

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