This clinical trial aim to evaluate the efficacy and safety of Pyrotinib in combination with nab-paclitaxel in patients with HER2-positive advanced breast cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
80
pyrotinib maleate tablets: 400mg orally once daily continunously nab-paclitaxel: 125mg/m2 iv d1、8 of each 21 day cycle, 6cycles.
Progress-free survival(PFS)
Baseline to measured date of progress or death from any cause
Time frame: three years
Objective response rate (ORR)
Baseline to measured stable disease
Time frame: three years
Clinical Benefit Rate (CBR)
The percentage of subjects with Complete Response, Partial Response, or Stable Disease at least 24 weeks
Time frame: three years
Disease control rate(DCR)
Rate of the patients with disease control
Time frame: three years
Overall survival (OS)
Baseline to measured date of death from any cause
Time frame: up to death
Safety (number of Participants with adverse events)
Adverse events Toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0. The number of Participants with adverse events will be recorded at each treatment visit.
Time frame: three years
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