The trial is a multi-center, open, observational registration study, which aims to evaluate the safety and efficacy of Camrelizumab (anti-PD-1 antibody) in the treatment of Chinese patients with advanced esophageal cancer in the real world.
Study Type
OBSERVATIONAL
Enrollment
1,030
The recommended formulation of Camrelizumab is 200 mg every time, or 3 mg/Kg according to body weight, intravenously infused.
Beijing Cancer Hospital
Beijing, Beijing Municipality, China
Adverse events of Camrelizumab
especially Occurrence of ≥Grade 3 immune-related AEs
Time frame: an expected average of 24 months
Adverse events of Camrelizumab
including other occasional or rare AEs
Time frame: an expected average of 24 months
Overall Survival
Duration from the date of initial treatment to the date of death due to any cause
Time frame: an expected average of 24 months
Progression-free Survival (PFS)
A duration from the date of initial treatment to radiographic disease progression or death of any cause
Time frame: an expected average of 24 months
Objective Response Rate (ORR)
Proportion of objective complete response and partial response patients
Time frame: an expected average of 24 months
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