This is a multi-center, retrospective, real-world study. The purpose of this study is to observe the effectiveness and safety of regorafenib in Chinese advanced colorectal cancer patients. The main observational goals include overall survival(OS), 6 month OS rate, 1 year OS rate, and treatment time failure (TTF), other study goals include objective response rate( ORR)、Disease control rate(DCR)and adverse event(AE) of regorafenib.
Study Type
OBSERVATIONAL
Enrollment
650
Cancer Hospital,Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, China
National Cancer Center/Cancer Hospital, Chinese ACademy of Medical Sciences and Peking Union Medical College
Beijing, China
6-month Overall Survival rate
6 months OS rate of patients who received regorafenib treatment.
Time frame: 6 month
1 year Overall Survival rate
1 year OS rate of patients who received regorafenib treatment.
Time frame: 1 year
overall survival
overall survival of patients who received regorafenib treatment.
Time frame: 1 year
objective response rate
Investigator assessed according to RECIST v1.1
Time frame: 1 year
Disease control rate
Investigator assessed according to RECIST v1.1
Time frame: 1 year
Incidence of Adverse Events (AEs)
Number of patients with AE, treatment-related AE (TRAE), AE of special interest (AESI), serious adverse event (SAE) assessed by CTCAE v5.0.
Time frame: 1 year
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