To evaluate the efficacy and safety of pyrotinib combined with capecitabine in patients with metastatic her-2 positive colorectal cancer after standard treatment.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
34
Pyrotinib in combination with capecitabine
Qingdao University Hospital
Qingdao, Shandong, China
Maximally Tolerated Dose (MTD)
Evaluation of tumor burden based on RECIST criteria.
Time frame: up to 36 months
Progression-free survival (PFS)
Evaluation of tumor burden based on RECIST criteria.
Time frame: up to 36 months
Objective Response Rate (ORR)
Evaluation of tumor burden based on RECIST criteria.
Time frame: up to 36 months
Duration Of Response (DOR)
Evaluation of tumor burden based on RECIST criteria.
Time frame: up to 36 months
Disease Control Rate (DCR)
Evaluation of tumor burden based on RECIST criteria.
Time frame: up to 36 months
Incidence of Treatment-Emergent Adverse Events [Safety]
Time frame: up to 36 months
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