This is an prospective, multicenter, single-arm clinical study.
Prospective, multicenter, single-arm clinical study of chemotherapy combined with bevacizumab neoadjuvant therapy for early or locally advanced HER2-negative breast cancer
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
75
All subjects enrolled will receive bevacizumab .Subjects continued to take medication until disease progression, unacceptable toxicity, withdrawal of informed consent, or discontinuation of medication at the discretion of the investigator.
The Fourth Hospital of Hebei Medical University
Shijiazhuang, Hebei, China
RECRUITINGPCR
pathologic complete response
Time frame: 24 months
ORR
objective response rate
Time frame: 24 months
AE Advese Event Advese Event breast conservation rates
Advese Event
Time frame: 24 months
BCR breast conservation rates
breast conservation rates
Time frame: 24 months
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