The purpose of this observational study is to evaluate the safety and efficacy of camrelizumab and apatinib in patients with advanced gastric cancer under real-life conditions, particularly in various subgroups of gastric cancer patients, with a view to providing information about the treatment modalities and efficacy of the treatment in real-life gastric cancer patients and to explore the possible predictive biomarkers of prognosis.Patients, who had both decided to be treated with camrelizumab or apatinib prior to enrollment, were entered into one of the following three cohorts at the discretion of the investigator, based on their disease stage and prior treatment
Study Type
OBSERVATIONAL
Enrollment
504
200mg,iv,d1,Q2W/Q3W
250mg,qd
Standard treatment
Changzhi People's Hospital Affiliated to Changzhi Medical College
Changzhi, Shanxi, China
RECRUITINGObjective response rate
The percentage of subjects achieving complete or partial response in a real-world clinical setting.
Time frame: 24 months
Progression free survival
From date of admission until the date of first documented progression in the real-world setting or date of death from any cause, whichever came first, assessed up to 24 months.
Time frame: 24 months
Disease control rate
The percentage of subjects achieving complete response, partial response, or disease stability in a real-world clinical setting.
Time frame: 24 months
Overall survival
From date of admission until the date of death from any cause, assessed up to 24 months.
Time frame: 24 months
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