This study is an open, multicenter, randomized controlled clinical trial for patients with newly diagnosed primary invasive breast cancer and clinical stage of T2 or above. The main purpose of this study is to evaluate the efficacy of dose-dense nab-paclitaxel compared with dose-dense docetaxel followed by anthracycline and cyclophosphamide in the treatment of HR positive and HER-2 negative breast cancer. The effectiveness and safety of the treatment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
nab-paclitaxel 260mg/m2 for every 2 weeks followed by anthracycline and cyclophosphamide
Docetaxel 100 mg/m2 for for every 2 weeks followed by anthracycline and cyclophosphamide
Xijing hospital
Xi'an, Shaanxi, China
RECRUITINGRCB
Residual tumor load
Time frame: 2 years
pCR
Complete remission of Pathology
Time frame: 2 years
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