The purpose of this study is to investigate the efficacy and safety of HIPEC plus apatinib and S-1 in the conversion therapy of gastric cancer with positive exfoliative cancer cells
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
38
HIPEC: 43℃, 60min. the drug is paclitaxel : 70mg/m2 d1 d3 d5, The interval is not less than 24h , A total of three times. apatinib:500mg qd po, 28 days is a cycle.preoperative 2 cycles, 2 cycles after surgery. S-1: According to the body surface area, BSA \<1.25m2,40mg bid; 1.25m2≤BSA≤1.5m2,50mg bid; BSA \>1.5m2, 60mg bid. Take the medicine twice daily for 2 weeks, then suspend for 1 week. preoperative 3 cycles, 3 cycles after surgery
R0-resection rate
There was no residual by the microscope
Time frame: within 3 weeks after surgery
Conversion to negative rate
Exfoliative cytology positive gastric cancer conversion to negative rate
Time frame: within 3 weeks after surgery
Overall survival (OS)
Baseline to measured date of death from any cause
Time frame: 5years
Progression free survival (PFS)
Baseline to measured date of progression or death from any cause
Time frame: 5years
Adverse events
Toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0.The number of Participants with adverse events will be recorded at each treatment visit
Time frame: 5 years
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