To evaluate the patterns and treatment outcomes of pyrotinib plus vinorelbine in the real world.
Study Type
OBSERVATIONAL
Enrollment
97
Fudan University Shanghai Cancer Center
Shanghai, Shanghai Municipality, China
PFS
Progression free survival
Time frame: 6 weeks
Adverse events
Number of participants with treatment-related adverse events as assessed by Common Terminology Criteria for Adverse Events version 4.0 (CTCAE v4.0)
Time frame: 6 weeks
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