A phase II trial evaluating intra-hepatic chemotherapy with oxaliplatin every second week in combination with systemic gemcitabine and capecitabine in combination with cetuximab in patient with non-resectable liver metastases from cholangiocarcinoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
56
Intrahepatic oxaliplatin
Oxaliplatin given intravenous
Herlev Hospital
Herlev, Denmark
PFS
Time from treatment start to progression or death.
Time frame: 6 months after last patient included
Response rate.
Time frame: 6 months after last patient included
Survival
Time frame: 6 months after last patient included
Toxicity
Time frame: 28 days after last treatment of last patient
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