Primary breast cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Histologically-proven breast cancer T1c-3N0M0/T1-3N1M0 No prior therapy for breast cancer Performance status 0-1 Adequate hematologic, renal, hepatic and cardica function Written informed consent
Exclusion criteria
Exclusion criteria: Hypersensitivity for drug Serious coexisting illness Active double cancer Bilateral breast cancer Male breast cancer Pregnant or postpartum women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety, clinical and histologic effect | — |
Secondary
| Measure | Time frame |
|---|---|
| Breast-conserving rate, disease-free survival | — |
Countries
Japan
Contacts
JBCRG Head Office