The aim of this study is to test the efficacy and safety of immunotherapy plus chemotherapy on people with a relatively rare type of gastric cancer. Participants will take the anti-PD-1 inhibitor (Tislelizumab) and platinum-based chemotherapy (oxaliplatin + capecitabine or oxaliplatin + S-1) in a 3-week cycle, followed by a radical operation after 6 cycles.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
53
Tislelizumab 200 mg will be administered systemically on day 1 of each cycle in all participants
Oxaliplatin 150 mg will be administered systemically on day 1 of each cycle in all participants
S-1 40 mg will be administered orally on day 1-14 of each cycle in all participants
Sun Yat-sen University Cancer Center
Guangzhou, Guangdong, China
RECRUITINGMPR
Major pathologic response, defined as less than 10% residual tumor following neoadjuvant therapy
Time frame: up to 2 years
Adverse Events
Time frame: up to 2 years
Incidence of surgical complications
Time frame: up to 2 years
Rate of R0 resection
Time frame: up to 2 years
OS
3-year overal survival
Time frame: up to 5 years
DFS
3-year disease-free survival
Time frame: up to 5 years
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Capecitabine 2500 mg will be administered orally on day 1-14 of each cycle in all participants