This study aimed to evaluate the use of SHR-A1811 in HER2-expression Advanced Breast Cancer patients with brain metastases.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
125
SHR-A1811: intravenous
Pyrotinib: oral
Bevacizumab: intravenous
Henan Cancer Hospital
Zhengzhou, Henan, China
RECRUITINGCNS-ORR by investigator
CNS-ORR was defined as percentage of participants with CNS response assessed by the investigator according to RANO-BM criteria
Time frame: 2 months
ORR by investigator using RECIST Guideline (Version 1.1)
ORR was defined as percentage of participants with best (confirmed) overall response (BOR) of either CR or PR assessed by the investigator according to RECIST version 1.1
Time frame: 2 months
PFS
PFS was defined as the time from first dose to first documented disease progression (PD) or death from any cause, whichever occurred first
Time frame: up to 1.5 years
Adverse events
Proportion of participants experienced adverse events during the study period
Time frame: up to 1.5 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.