The purpose of this study is to evaluate the efficacy and safety of nab-PTX and trastuzumab for ER negative and HER2 positive operable (tumor size of 3cm or less and N0) breast cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
nab-paclitaxel 260mg/m2 q3w
trastuzumab 6 mg/kg (8 mg/kg as the loading dose)
Osaka Medical College
Takatsuki, Osaka, Japan
Pathological complete response rate
Time frame: Up to 12 weeks after the protocol therapy
Disease free survival
Time frame: Five years after the last patient enrolled
Objective response rate
Time frame: Up to 6 weeks after the protocol therapy
Pathological response rate
Time frame: Up to 12 weeks after the protocol therapy
Breast-conserving surgery rate
Time frame: Up to 6 weeks after the protocol therapy
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Time frame: Up to 6 weeks after the protocol therapy
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