To evaluate the efficacy and safety of T-DXd in the treatment of HER2-positive breast cancer with brain metastases after treatment with pyrotinib
Study Type
OBSERVATIONAL
Enrollment
30
Efficacy and safety of T-DXd in the treatment of HER2-positive breast cancer with brain metastases after treatment with pyrotinib
The Fifth Medical Center of PLA General Hospital
Beijing, Beijing Municipality, China
RECRUITINGThe Fifth Medical Center of PLA General Hospital
Beijing, Beijing Municipality, China
RECRUITINGCentral neryous system Progression Free Survival,CNS-PFS
The interval from the start of treatment to the onset of disease progression or death from any cause in the intracranial lesions
Time frame: 3years
Overall Response Rate (ORR)for intracranial and extracranial lesions
Percentage of patients with CompleteResponse (CR) and partial response (PartialResponse (PR)
Time frame: 3years
Overall Clinical Benefit Rate (CBR) for intracranial and extracranial lesions
Percentage of patients with complete response, partial response, and StableDisease (SD)≥6 months
Time frame: 3years
Overall survival (Oversall Survival, OS) and security
The interval between the start of treatment and death from any cause
Time frame: 5years
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