This is an open-label, phase II study to evaluate the efficacy and safety of a modified regimen of oxaliplatin and capecitabine on metastatic colorectal adenocarcinoma in the first-line therapy.
Primary endpoint: Overall Response Rate Secondary endpoint: Time to progression, overall survival, safety data
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Oxaliplatin 85mg/m2 D1 and capecitabine 1g/m2 BID D1-D10, repeat every two weeks. Efficacy will be evaluated every three cycles.
the Sixth Affiliated Hospital of Sun Yat-sen University
Guangzhou, Guangdong, China
RECRUITINGOverall response rate according to RECIST 1.1
Time frame: One year
Time to progression
Time frame: One year
overall survival
Time frame: One Year
Safety data of this regimen
Time frame: One Year
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