Back to resultsA Study of the Advanced Adenocarcinoma of Stomach and Gastroesophageal Junction With Camrelizumab+SOX Control Camrelizumab+SOX+ Trastuzumab
Advanced Gastric Adenocarcinoma
About this trial
This is an interventional treatment trial for Advanced Gastric Adenocarcinoma
Eligibility Criteria
Inclusion Criteria:
1) Age 18-75 years old; Male or female; 2) Histopathological examination of gastroscopy biopsy confirmed adenocarcinoma of stomach and gastroesophageal junction; 3) Imaging (CT/MRI) and ultrasonic gastroscopy confirmed that: cT≥T2 and/or regional lymph node positive (N+); 4)HER-2 positive is the test result of IHC3+ or IHC2+/FISH+, and HER-2 test score standard refers to her-2 test guide for gastric cancer; 5)ECOG score: 0~1; 6) The expected survival time is ≥ 12 weeks; 7) The main organ functions meet the following criteria within 7 days before treatment:
Blood routine examination standard (without blood transfusion within 14 days):
Hb ≥ 90g/l; The absolute value of neutrophils (ANC) ≥ 1.5× 109/L; Platelet (PLT) ≥ 80× 109/L;
- Biochemical examination shall meet the following standards:
Total bilirubin (TBIL)≤1.5 times the upper limit of normal value (ULN); Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5× ULN; Serum creatinine (Cr)≤1.5 ULN or creatinine clearance rate (CCR) ≥ 60ml/min; (3) Doppler ultrasound evaluation: Left ventricular ejection fraction (LVEF) ≥ the lower limit of normal value (50%).
8) Women of childbearing age should agree to take contraceptive measures (such as intrauterine device, contraceptive pill or condom) during the study period and within 6 months after the end of the study; Serum or urine pregnancy test was negative within 7 days before the study was enrolled in the group, and it must be a non-lactating patient; Men should agree to patients who must use contraception during the study period and within 6 months after the end of the study period.
9) Patients volunteered to participate in this study and signed an informed consent form;
Exclusion Criteria:
1) have had or are currently suffering from other malignant tumors within 5 years, except cured cervical carcinoma in situ, non-melanoma skin cancer and superficial bladder tumor [Ta (non-invasive tumor), Tis (cancer in situ) and T1 (tumor infiltrating basement membrane)]; 2) Patients with distant metastasis and unable to undergo surgical resection; 3) Have a history of mental illness, or abuse of psychotropic drugs; 4) Subjects with diseases requiring systemic treatment with glucocorticoid (> 10 mg prednisone equivalent dose per day) or other immunosuppressive drugs within 14 days before the start of study treatment. In the absence of active autoimmune diseases, it is allowed to use inhaled or topical steroids > 10 mg daily prednisone equivalent dose and adrenal replacement steroid dose; 5) Those who have received any anti-tumor treatment in the past; 6) Participants who receive live/attenuated vaccines within 30 days; 7) Allergic reactions and adverse drug reactions:
- History of allergy to the ingredients of the study drug;
Contraindications of any study drug (oxaliplatin or S-1) in chemotherapy regimen.
8) Patients with any severe and/or uncontrollable diseases, including:
- Patients with hypertension who can't get good control after antihypertensive drug treatment (systolic blood pressure ≥180 mmHg, diastolic blood pressure ≥100 mmHg);
- Suffering from grade I or above myocardial ischemia or myocardial infarction, arrhythmia (including QTc≥480 ms) and grade 2 or above congestive heart failure (new york Heart Association (NYHA) classification);
- Severe or uncontrolled disease or active infection (≥ CTCAE level 2 infection), which the researcher believes will increase the risks related to research participation, administration of research drugs or affect the ability of subjects to receive research drugs;
- Renal failure requires hemodialysis or peritoneal dialysis;
- those who have a history of immunodeficiency diseases, including HIV-positive or other acquired and congenital immunodeficiency diseases, or have a history of organ transplantation; 9) Patients with a large number of ascites or poor ascites control; 10) preparing for or receiving allogeneic organ or allogeneic bone marrow transplantation, including liver transplantation; 11) Patients with brain metastasis; 12) Patients who are not suitable to participate according to the researcher's judgment.
Sites / Locations
- Henan Tumor HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Cohort 1
Cohort 2
camrelizumab was administered intravenously at a fixed dose of 200 mg, on the first day, once every 3 weeks, with a cycle of 3 weeks. Infusion for 30 min each time (no less than 20 min and no more than 60min); SOX: Oxaliplatin: 130 mg/m2, administered intravenously, on the first day, once every three weeks, and every three weeks is a cycle; S-1: according to BSA (< <1.25 40 mg；; 1.25-1.5 50 mg； > >1.5 60 mg), oral administration, d1-d14 twice a day, 3 weeks as a cycle; Trazumab was administered intravenously, with an initial loading dose of 8 mg/kg and a subsequent dose of 6 mg/kg, with a cycle of 3 weeks
camrelizumab was administered intravenously at a fixed dose of 200 mg, on the first day, once every 3 weeks, with a cycle of 3 weeks. Infusion for 30 min each time (no less than 20 min and no more than 60min); SOX: Oxaliplatin: 130 mg/m2, administered intravenously, on the first day, once every three weeks, and every three weeks is a cycle; S-1: according to BSA (< <1.25 40 mg；; 1.25-1.5 50 mg； > >1.5 60 mg), oral administration, d1-d14 twice a day, 3 weeks as a cycle;
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
1. Study Identification
2. Study Status
3. Sponsor/Collaborators
4. Oversight
5. Study Description
6. Conditions and Keywords
7. Study Design
8. Arms, Groups, and Interventions
10. Eligibility
12. IPD Sharing Statement
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