To investigate the real-world efficacy and safety of Sacituzumab govitecan for HER2 negative metastatic breast cancer patients in China.
This study will conduct a multicenter, open, prospective clinical trial to investigate the real-world efficacy and safety of Sacituzumab govitecan for HER2 negative metastatic breast cancer patients in China.
Study Type
OBSERVATIONAL
Enrollment
200
Zhejiang Cancer Hospital
Hangzhou, Zhejiang, China
RECRUITINGPFS
Progression-Free Survival
Time frame: from enrollment to progression or death (for any reason),assessed up to 100 months
Objective Response Rate
Ratio of CR and PR in all subjects
Time frame: from enrollment to progression or death (for any reason), assessed up to 100 months
DoR
Duration of Response
Time frame: The first evaluation of CR or PR to progression or death (for any reason),assessed up to 100 months
OS
Overall Survival
Time frame: from enrollment to death (for any reason).assessed up to 100 months
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