A open-label, single-arm, phase II trial to study was designed to evaluate the effectiveness and safety of trastuzumab and pyrotinib in treating HER2 positive patients who have previously treated, locally advanced, or metastatic urothelial carcinoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
A loading dose of trastuzumab 8mg/kg IV over 90 minutes will be administrated on day 1 of week 1. For all subsequent doses, trastuzumab 6mg/kg IV over 30 minutes will be administrated every three weeks. Pyrotinib 400mg PO daily will be administrated at the same time.
National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
Beijing, China
RECRUITINGORR
Objective response rate as assessed by RECIST criteria
Time frame: 1 year
OS
Overall survival
Time frame: From date of initiation of treatment to date of death due to any cause, assessed up to 2 years
PFS
Progression free survival
Time frame: From date of initiation of treatment to date of progression or death due to any cause, whichever occurs first, assessed up to 2 years
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