The aim of this single center, single arm and prospective study is to explore the safety and efficacy of tumor antigen-sensitized DC vaccine in postoperative adjuvant treatment of esophageal cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
25
subcutaneous administration
West China Hospital
Chengdu, Sichuan, China
Number of participants with treatment-related adverse events as events as assessed by CTCAE v4.0
Number of participants with treatment-related adverse events as events as assessed by CTCAE v4.0
Time frame: 3 months after the last administration of cells
Disease-free Survival
Number of participants with Disease-free Survival as assessed by RECIST1.1
Time frame: through study completion, an average of 1 year
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