This Non-Interventional Study will describe and analyze the clinical use of pyrotinib in clinical practice in the treatment of HER2 positive breast cancer in the real world.
Study Type
OBSERVATIONAL
Enrollment
3,000
This prospective, observational study will be conducted according to each site's routine clinical practice
National Cancer Center, Cancer Hospital/Chinese Academy of Medical Sciences and Peking Union Medical College
Beijing, Beijing Municipality, China
RECRUITINGProgression Free Survival(PFS)
Progression Free Survival(PFS)
Time frame: 12 months
Pathological Complete Response(pCR)Rate
Percentage of Participants With Pathological Complete Response
Time frame: through study completion, an average of 1 year
Incidences of adverse events and toxicities
Incidences of adverse events and toxicities
Time frame: through study completion, an average of 1 year
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