Randomised Phase II Study of the Combination of Oral Vinorelbine With Capecitabine Versus Gemcitabine in Combination With Paclitaxel Versus Gemcitabine in Combination With Docetaxel as First Line Chemotherapy in Patients With Metastatic Breast Cancer

PM0259CA223B0

The aim of this international open-label randomized phase II trial is to evaluate the efficacy and safety of an all-oral combination and two all-intravenous combinations as first-line therapy for HER2-negative mBC patients.

2007-03-27

2013-04-18

2013-04-18

Completed

Early phase I

152

Inclusion Criteria: * Histologically confirmed adenocarcinoma of the breast; * Documented metastatic disease previously untreated by chemotherapy; * HER2 negative (assessed by 0-1+ IHC or 2+ IHC with FISH-) on the primary tumor or on metastatic site; * Karnofsky Performance Status 70%. Exclusion Criteria: * Local relapse alone after conservative treatment or contra-lateral tumor; * Patients with symptoms suggesting CNS involvement or leptomeningeal metastases; * Concomitant hormonal therapy for metastatic breast cancer; * Prior chemotherapy in the metastatic setting; * Patients previously treated with a vinca-alkaloid, capecitabine, gemcitabine or taxanes; * Prior severe and unexpected reaction to fluoropyrimidine therapy (with or without documented DPD deficiency) or known hypersensitivity to 5-fluorouracil.

{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 152, 'type': 'ACTUAL'}}

2024-04-30