This study is a prospective, randomized, two-cohort trial designed to evaluate the efficacy and safety of two regimens in the treatment of gastric or gastroesophageal junction adenocarcinoma with peritoneal metastasis: SHR-1701 combined with intravenous and intraperitoneal paclitaxel plus S-1, or SHR-1701 combined with CAPOX.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
60
Changhai Hospital
Shanghai, Shanghai Municipality, China
RECRUITINGRuijin Hospital, Shanghai Jiaotong University School of Medicine
Shanghai, China
RECRUITING2-year overall survival rate
Time frame: Up to 2 years
Conversion surgery rate
Time frame: Up to 4 weeks after completion of surgery
R0 resection rate
Time frame: Up to 4 weeks after completion of surgery
Pathological complete response(pCR)
Time frame: Up to 4 weeks after completion of surgery
Tumor regression grade
Time frame: Up to 4 weeks after completion of surgery
Event free survival (EFS)
Time frame: Up to 2 years
DFS
Disease-free survival (DFS)
Time frame: Up to 2 years
Overall survival(OS)
Time frame: Up to 3 years
AEs
Time frame: Up to 3 years
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Paclitaxel,Q3W
Oxaliplatin, Q3W