This is a prospective, single-center, open, historically controlled real-world study. The aims of this study is to evaluate the safety and effectiveness of Nab-paclitaxel combined with oxaliplatin and S-1 in the treatment of patients with advanced gastric cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Nab-paclitaxel 100mg/m\^2, D1, Q3W; oxaliplatin 85 mg/m\^2, D1, Q3W; S-1 60 mg/m\^2, D1-14, Q3W; Neoadjuvant chemotherapy 2 cycles, followed by surgery, continue to receive 6 cycles of adjuvant chemotherapy.
The First Affiliated Hospital of the Air Force Medical University
Xi'an, China
RECRUITINGAE
Number of participants with treatment-related adverse events as assessed by NCI-CTCAE V5.0
Time frame: 2-year
Objective response rate (ORR)
ORR is defined as the rate of complete response (CR) or partial response (PR), as determined by IRC using RECIST v1.1 criteria among patients with at least one target lesion.
Time frame: 7-month
Disease Control Rate (DCR)
The proportion of all subjects who assessed the best overall curative effect as CR, PR, and disease stable (SD) according to the RECIST 1.1 standard.
Time frame: 7-month
Overall survival (OS)
It is defined as the time from the first doses durg to the time of death due to any reason.
Time frame: 2-year
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