The purpose of this study is to determine if sorafenib, capecitabine and oxaliplatin (SECOX) regimen is more effective than sorafenib alone in the treatment of advanced liver cancer.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
46
Queen Mary Hospital
Hong Kong, Hong Kong
Time to progression (TTP)
Time from study treatment to radiological progression
Time frame: Approximately 18 months
Objective Response Rate (ORR)
Proportion of patients with a complete response (CR) or partial response (PR)
Time frame: Approximately 18 months
Progression-free survival (PFS)
Time from study treatment to radiological disease progression or death due to any causes
Time frame: Approximately 18 months
Overall survival (OS)
Time from study treatment to the date of death due to any cause or last follow-up date
Time frame: Approximately 33 months
Frequency and severity of adverse events and laboratory abnormalities
Type, frequency, severity of adverse events (AEs) and laboratory abnormalities as graded by NCI CTCAE v4.03, and their seriousness and relationship to study medications
Time frame: Approximately 18 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.