In this study, we compared first-line VIC regimen with chemotherapy plus bevacizumab in Chinese patients with initially unresectable BRAF V600E-mutated mCRC. The principal goal was to evaluate the safety of VIC regimen, and to investigate the tumor response, the radical resectability, and the patient survival.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
78
VIC Regimen (Vemurafenib/Irinotecan/Cetuximab)
Bevacizumab Plus Doublet or Triplet Chemotherapy
Department of General Surgery, Zhongshan Hospital, Fudan University
Shanghai, China
RECRUITINGprogression-free survival
time from first study treatment to the first documented progression disease or death, whichever occurred first
Time frame: 3 years
overall survival
time from first study treatment to death from any cause.
Time frame: 3 years
objective response rate
the proportion of patients with complete response or partial response.
Time frame: 6 months
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