Breast Cancer Clinical Trial
Official title:
An Open-Label Study of PROCRIT (Epoetin Alfa) in Women Undergoing Adjuvant Chemotherapy for Stage I, II, or III Breast Cancer
RATIONALE: Epoetin alfa may stimulate red blood cell production to treat patients who have
anemia following chemotherapy.
PURPOSE: Phase IV trial to study the effectiveness of epoetin alfa in treating
chemotherapy-related anemia in women who have stage I, stage II, or stage III breast cancer.
OBJECTIVES: I. Determine the effectiveness and safety of epoetin alfa in patients receiving
adjuvant chemotherapy for stage I, II, or III breast cancer. II. Determine the clinical
outcomes in these patients receiving this drug.
OUTLINE: This is a multicenter study. Patients receive epoetin alfa subcutaneously once
weekly for up to 24 weeks in the absence of unacceptable toxicity. Quality of life is
assessed at baseline, at week 13, and at study completion.
PROJECTED ACCRUAL: A maximum of 2,500 patients will be accrued for this study.
;
Primary Purpose: Supportive Care
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