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Differential gene regulation during neoadjuvant therapy trial of Epirubicin/cyclophosphamide (EC) docetaxel/capecitabaine (DX) regimens in patients with large ER-positive and ER-negative breast cancer, a randomized Phase II Trial
- Objective
- The chemotherapy drugs are epirubicin, cyclophosphamide and docetaxed, given by IV infusion, and capecitabine, given by mouth.
- IRB Protocol Number
- 02-824-A
- Principal Investigator(s)
- ANTHONY ELIAS
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- Sponsor(s)
- Contact
- ANNA NELSON at 720-848-0675
or ANNA.L.NELSON@UCDENVER.EDU
- Eligibility and Other Participant Information
- What To Expect : There are two different treatments for this trial. Group 1 will receive epirubicin and cyclophosphamide before breast cancer surgery, followed by a combination of dectaxel and capecitabine after surgery. Group 2 will receive docetaxed and capecitabine before surgery, followed by a combination of epirubicin and cyclophosphamide after surgery. The study will last about 8-9 months. We will follow you for life by phone contact. // Eligibility criteria include but are not limited to patients 18 years or older with newly diagnosed breast cancer. There will be a screening period to determine eligibility
Location
- University of New Mexico Cancer Center