The purpose of this study is to assess the efficacy and safety of patients who receive apatinib single or combined capecitabine for treatment of patients with metastatic her-2 negative breast cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
120
apatinib 500mg qd po or combined capecitabine 1000mg/m2 bid d1-14 q3w
Fourth Hospital of Hebei Medical University
Shijiazhuang, Hebei, China
RECRUITINGProgression free survival
Baseline to measured date of progression or death from any cause
Time frame: evaluated in 24 months since the treatment began
Overall survival
Baseline to measured date of death from any cause
Time frame: the first day of treatment to death or last survival confirm date,up to 24 months
Disease control rate
Baseline to measured progressive disease
Time frame: tumor assessment every 6 weeks since the treatment began,up to 24 months
Objective response rate
Baseline to measured stable disease
Time frame: tumor assessment every 6 weeks since the treatment began,up to 24 months
Side effects
throughout study
Time frame: evaluated in the 24th month since the treatment began according to the Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.