Breast Cancer Clinical Trial
Official title:
A Pilot Study of Cytoxan, Epirubicin, and Capecitabine in Women With Stage I/II/IIIA Breast Cancer
The purpose of this study is to find out what effects (good and bad) a combination of cytoxan, epirubicin, and capecitabine have on women with Stage II/II/IIIA breast cancer.
- Each treatment cycle lasts 21 days and patients will participate in a least 4 cycles,
but no more than 6 cycles of treatment.
- Patients will receive cytoxan (cyclophosphamide) and epirubicin intravenously on day 1
of each treatment cycle. On days 4-17 of each cycle, patients will take capecitabine
orally twice a day.
- While on the study patients will be required to complete a diary of they capecitabine
treatment.
- Blood tests will be performed each week along with surveys at the beginning of the
trial and certain follow-up visits to evaluate the patient's experience with the oral
chemotherapy.
- Patients will be on the treatment for 12-18 weeks depending upon whether or not the
disease progresses or the patient develops inacceptable side effects.
;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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