Status:
UNKNOWN
Camrelizumab Combined With SOX and/or Apatinib for Locally Advanced Gastric Cancer
Lead Sponsor:
First Affiliated Hospital Xi'an Jiaotong University
Collaborating Sponsors:
Jiangsu HengRui Medicine Co., Ltd.
Conditions:
Locally Advanced Gastric Cancer
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
This study was designed to evaluate the efficacy and safety of camrelizumab in combination with SOX and/or apatinib in the treatment of locally advanced gastric cancer or gastroesophageal junction ade...
Detailed Description
Screening period Subjects will enter the study screening period after signing the informed consent, and the maximum screening period will be 28 days. Those who meet all the inclusion criteria and do n...
Eligibility Criteria
Inclusion
- Voluntarily sign written informed consent before screening;
- Male or female, ≥18 years old;
- Have at least one measurable lesion according to RECIST1.1;
- ECOG physical status score 0\~1;
- Pathologically confirmed local progression (CT3/CT4N+M0) of gastric cancer or adenocarcinoma of the gastroesophageal junction without any previous treatment (Siewert II or III).
- According to the clinical staging standard, surgical treatment is planned after neoadjuvant chemotherapy.
- Expected survival of more than 3 months;
- The main organs function normally, following criteria:
- I. Blood routine (no blood transfusion, no use of granulocyte colony stimulating factor (G-CSF) or other hematopoietic stimulating factor correction within 14 days before screening examination) : neutrophils ≥1.5× 109 /L, platelets ≥100×109/L, hemoglobin ≥90g/L;White blood cells acuity 3.5 x l09 / L II. Liver function: ALT and AST, ALT and AST ≤ 2.5×ULN; Total bilirubin (TBil) ≤ 1.5×ULN (Gilbert syndrome patients, ≤ 3×ULN); III. Renal function: serum creatinine (CR) ≤ 1.5×ULN or creatinine clearance (CCR) ≥60mL/ min; IV. Coagulation function: APTT, INR, PT ≤ 1.5×ULN;
Exclusion
- Gastric squamous cell carcinoma, adenosquamous cell carcinoma, small cell carcinoma and undifferentiated gastric carcinoma confirmed by pathology;
- Positive HER-2 test (IHC3+ or IHC2+ amplified by FISH);
- Any previous anti-tumor therapy (including chemotherapy, radiotherapy, hormone therapy, and molecular targeted therapy);
- Cardiac and pyloric obstruction affects the patient's eating and gastric emptyor and has difficulties to swallow tablets;
- Previous immunotherapy with anti PD-1, anti PD-L1, anti PD-L2, anti CD137 or anti CTLA-4 antibodies or any other antibodies or drugs that target co-stimulation of T cells or immune checkpoint pathways;
- Has developed or is currently having other malignant tumors within 5 years, except for cured cervical carcinoma in situ, non-melanoma skin cancer, or other tumors/cancers that have undergone radical treatment and have been free of disease for at least 5 years;
- Perimeter neuropathy is grade 2 or greater according to the common adverse event terminology (NCI-CTCAE V5.0);
- with known active central nervous system metastases (CNS) and/or cancerous meningitis;
- Any component of a product or preparation similar to the study drug PD-1 monoclonal antibody has ever caused a severe allergic reaction, including known severe allergic reaction to other monoclonal antibodies, oxaliplatin, S-1 and other related compounds (NCI-CTCAE V5.0≥3);
- a known history of hereditary bleeding or a blood clotting disorder that is at risk of bleeding;
- Patients who underwent major surgery within 4 weeks;
- Subjects who did not recover from complications from previous surgery, i.e., did not drop to ≤1 (CTCAE version 5.0) (excluding hair loss and fatigue);
- Immunosuppressive drugs should be used for 2 weeks or within 2 weeks or during the study, excluding the following situations:
- A) Intranasal, inhaled, topical or topical steroid injections (e.g. intraarticular); B) Systemic corticosteroids at physiological dose (≤10mg/day prednisone or equivalent); C) short-term (≤7 days) use of steroids to prevent or treat non-autoimmune allergic diseases;
- Subjects with active or preexisting autoimmune diseases that are likely to recur;
- Subjects with a known history of idiopathic pulmonary fibrosis, drug-induced pneumonia, histological pneumonia, or non-infectious pneumonia;
- known active tuberculosis history;
- A history of human immunodeficiency virus infection (HIV positive), other acquired or congenital immunodeficiency diseases, or a history of organ transplantation, or stem cell transplantation;
- The hepatitis B or C virology test meets any of the following criteria at the time of screening:
- A) HBsAg positive, and the titer of HBV-DNA in peripheral blood ≥104 copy number /mL or ≥2000IU/mL (HBV carriers should be treated with antiviral therapy by the researcher as appropriate); B) Active hepatitis C: HCV antibody positive and HCV-RNA higher than the detection limit of the analytical method;
- Subjects had active or uncontrollable infections requiring systematic treatment within 2 weeks before randomization;
- have received live virus vaccine within 4 weeks;
- The presence of uncontrollable pleural effusion, pericardial effusion or ascites requiring repeated drainage or medical intervention;
- gastrointestinal perforation and/or fistula occurred within 6 months, and gastrointestinal bleeding of clinical significance occurred within 3 months before randomization;
- have intestinal obstruction or the following diseases or history: inflammatory bowel disease or general bowel resection (partial colon resection or general small bowel resection with chronic diarrhea), Crohn's disease, ulcerative colitis or chronic diarrhea;
- with severe medical problems, such as level III and above abnormal cardiac function (NYHA), ischemic heart disease (such as myocardial infarction, or angina pectoris) such as cardiovascular disease, or a history of myocardial infarction , within 3 months after the drug of poorly controlled diabetes (FPG)≥10mmol/L) or poorly controlled hypertension, systolic blood pressure≥160mmHg and/or diastolic blood pressure≥100mmHg;
- Subjects who are lactating or who plan to become pregnant during treatment and within 6 months after treatment;
- subjects who are unwilling to receive effective contraceptives during treatment and within 6 months after treatment (including male subjects who are capable of making a woman pregnant and female subjects and their male partners);
- The investigator believes that subjects are not suitable for the study because of other conditions that may affect their compliance with the protocol and evaluation of the study indicators.
Key Trial Info
Start Date :
January 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2022
Estimated Enrollment :
67 Patients enrolled
Trial Details
Trial ID
NCT04792515
Start Date
January 1 2021
End Date
December 31 2022
Last Update
March 11 2021
Active Locations (1)
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1
The First Affiliated Hospital of Xi 'an Jiaotong University
Xi'an, Shaanxi, China