This is a prospective, open label study to evaluate the efficacy and safety of neoadjuvant pyrotinib in early breast cancer patients.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
53
dual HER2 blockade in the neoadjuvant setting
Renji Hospital
Shanghai, China
pCR
pathological complete response
Time frame: 1-2 weeks after surgery
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