Advanced Gastric Cancer Clinical Trial
Official title:
Camrelizumab Combined With Apatinib Mesylate Tablets, Nab-paclitaxel and S-1 in the Treatment of Locally Advanced Gastric Cancer: an Multicenter, Open, Randomized, Controlled Clinical Study
Verified date | September 2023 |
Source | Fujian Medical University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To evaluate the clinical efficacy and safety of camrelizumab combined with apatinib mesylate, nab-paclitaxel and S-1
Status | Active, not recruiting |
Enrollment | 53 |
Est. completion date | March 31, 2025 |
Est. primary completion date | July 22, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - Age: 18-75 years of age - Gastric adenocarcinoma was confirmed by pathology( including histology or cytology)? - CT/MRI,PET-CT or laparoscopic exploration were used to confirm the diagnosis of gastric cancer staging as cT2-4a and/or N+ and M0 before operation. - measurable lesions at least should be detected by CT/MRI examination in accordance with the RECIST1.1.(CT scan of tumor lesion length=10mm,CT scan short diameter=15mm,scan slice thicknes 5mm) - ECOG(Eastern Cooperative Oncology Group)PS(Performance Status):0-1 scores; - the expected survival time is more than 12 weeks - the main organ function is normal, which should meet the following criteria: (1) blood routine examination standards should be met(no blood transfusion within 14 days) a.HB= 100g/L b. WBC=3×109/L c. ANC=1.5×109/L d. PLT=100×109/L (2)biochemical examination shall comply with the following criteria: 1. BIL<1.5 normal upper limit ULN 2. ALT and AST<2.5 ULN,GPT=1.5×ULN 3. Cr=1 ULN,CCR(creatinine clearance rate)>60ml/min(Cockcroft-Gault formula) - women of childbearing age must have a pregnancy test in 7 days before entering the group (in serum), and the results were negative, and willing to use appropriate contraception during the study period and the last 8 weeks after giving drug test; men should have the surgical sterilization, or adopt the appropriate contraceptive methods during the test and the last 8 weeks after giving drug test? - No other clinical studies were conducted before and during the treatment - participants is willing to participate in this study, sign the informed consent, have good compliance, cooperate with follow-up. Exclusion Criteria: - Previous history of chemotherapy, radiotherapy, targeted drug therapy or immunotherapy - Patients with contraindications for surgical treatment and chemotherapy or whose physical condition and organ function do not allow for larger abdominal surgery - patients with metastasis - Having any active autoimmune diseases or a history of autoimmune diseases (such as interstitial pneumonia, uveitis, enteritis, hepatitis, pituitary inflammation, vasculitis, myocarditis, nephritis, hyperthyroidism, hypothyroidism, including but not limited to these diseases or syndromes); Patients with vitiligo or cured childhood asthma/allergies who did not need any intervention in adulthood were excluded; Autoimmune hypothyroidism treated with a stable dose of thyroid replacement hormone; Type 1 diabetes with stable doses of insulin - A history of immunodeficiency, including HIV testing positive, or other acquired or congenital immunodeficiency disorders, or a history of organ transplantation and allogeneic bone marrow transplantation - Accompanied by serious heart, lung, liver, kidney disease; Have nerve, mental disease; Jaundice or obstruction of the digestive tract with severe infection - pregnant or lactating women - The blood pressure of patients with hypertension cannot be reduced to the normal range by the antihypertensive drugs (systolic pressure >140 mmHg, diastolic pressure >90 mmHg) - With ? magnitude of coronary heart disease, arrhythmia (including QTc protracted between male > 450 ms, women > 470 ms) and cardiac insufficiency - Patients have a clear tendency with gastrointestinal bleeding, including the following situation: local active ulcerative lesions, and fecal occult blood (+ +); with melena and hematemesis history in 2 months; and patients with fecal occult blood (+) and unresected gastric primary tumor; patients with the risk of bleeding should take the gastroscopy test, if it is the gastric cancer, and researchers believe that may results in massive digestive tract hemorrhage;coagulation dysfunction (INR(international normalized ratio)>1.5, APTT(activated partial thromboplastin time)>1.5 ULN), with bleeding tendency; - Subjects have failed to control good cardiovascular clinical symptoms or disease, including but not limited to: such as: (1) the NYHA class II heart failure (2) above unstable angina pectoris (3) occurred within 1 year (4) have clinical significance of myocardial infarction (mi) room sex or ventricular arrhythmias without clinical intervention on or after clinical intervention is still poorly controlled - History of interstitial lung disease (except radiation pneumonia without hormone therapy), and history of non-infectious pneumonia - Patients are positive of urine protein (urine protein detection 2+ or above, or 24 hours urine protein quantitative >1.0g); - A person who has previously been allergic to any component of camrilizumab or to any component of the drug under study - The researchers consider those who were not suitable for inclusion. |
Country | Name | City | State |
---|---|---|---|
China | Fujian Medical University Union Hospital | Fuzhou | Fujian |
Lead Sponsor | Collaborator |
---|---|
Fujian Medical University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | major pathological response | major pathological response(MPR) | 4 months | |
Secondary | pathological complete response | pathological complete response (pCR) | 4 months | |
Secondary | Objective response rate | Objective response rate (ORR) according to Response Evaluation Criteria in Solid Tumours (RECIST) version. 1.1, and immune-related (ir) RECIST | 4 months | |
Secondary | R0 resection rate | The surgical procedure was total or subtotal gastrectomy with 3 weeks after total neoadjuvant therapy. | 4 months |
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