First-line Treatment with RC48 Plus Tislelizumab and S-1(RCTS) in Advanced Gastric Cancer

Exclusion Criteria

• •1. Allergy to any trial drug and its excipients, or serious allergy history, or contraindication of the trial drug;
• •2. Cardiovascular and cerebrovascular events that are not well controlled, such as:
• •1. NYHA grade 2 or above heart failure;
• •2. Unstable angina pectoris;
• •3. Myocardial infarction occurred within 1 year;
• •4. Supraventricular or ventricular arrhythmia with clinical significance needs treatment or intervention;
• •5. Cerebral hemorrhage and cerebral infarction (except for lacunar cerebral infarction without symptoms and without treatment);
• •6. Serious cardiovascular and cerebrovascular events occurred within 12 months;
• •7. Uncontrolled hypertension, i.e. systolic blood pressure\>140 mmHg or diastolic blood pressure\>90 mmHg after single drug treatment;
• •8. Patients with history of arterial thrombosis or deep vein thrombosis within 6 months before recruitment, or with evidence of bleeding tendency or medical history within 2 months before recruitment, regardless of the severity;
• •9. Stroke event or transient ischemic attack occurred within 12 months before recruitment;
• •3. Has received systematic treatment with Chinese patent medicine or immunomodulatory drugs (including thymosin, interferon, interleukin, except for local use for ascites control) before the first administration within 2 weeks.
• •4. Have a history of interstitial lung disease, non-infectious pneumonia, pulmonary fibrosis, acute lung disease, or systemic disease with poor control (including but not limited to diabetes, hypertension, etc.);
• •5. Have a history of active immune deficiency or autoimmune diseases, including HIV positive test, or have other acquired or congenital immune deficiency diseases, or have a history of organ transplantation or autoimmune diseases;
• •6. Severe chronic or active infection requires systemic antibacterial, antifungal or antiviral treatment, including tuberculosis infection.Have a history of active tuberculosis infection ≥ 1 year before recruitment should also be excluded, unless proved has been completed appropriate treatment;
• •7. Brain metastasis or leptomeningeal metastasis;
• •8. Clinically significant pleural effusion, pericardial effusion or ascites should be drained for many times within 2 weeks before the first administration of the trial drug;
• •9. Has a second clinically detectable primary malignant tumor at the time of recruitment, or there were other malignant tumors in the past 5 years (except for fully treated skin basal cell carcinoma or cervical carcinoma in situ);
• •10. Any major surgery was performed ≤ 28 days before the first trial drug administration;
• •11. History of allogeneic stem cell transplantation or organ transplantation;
• •12. Duodenal ulcer, ulcerative colitis, intestinal obstruction and other gastrointestinal diseases at present; or other conditions that may cause gastrointestinal bleeding or perforation judged by the researchers; or history of intestinal perforation or fistula, but has not recovered after surgical treatment;
• •13. Live vaccine was inoculated within 4 weeks (inclusive) before the first administration of the trial drug, not including seasonal influenza vaccines but intranasal vaccine.
• •14. Has other factors that may lead to the forced termination of this trial according to the judgment of the investigator, such as other serious diseases (including psychological and mental diseases) requiring combined treatment, serious laboratory examination abnormalities, and family or social factors, which may affect the safety of the subject, or the collection of data and samples;
• •15. Participating in other therapeutic clinical studies or using research instruments within 4 weeks before the first administration;
• •16. Others conditions do not meet the inclusion according to the judgment of the investigator.