💬In plain words
What the trial is, and whether it could suit you
The FOLFIRINOX regimen has become the standard treatment regimen for advanced colorectal cancer, advanced pancreatic cancer and postoperative adjuvant treatment for pancreatic cancer. With the continuous exploration of Chinese scholars, it has also revised the modified dose suitable for the physical fitness of the Chinese people, which is well tolerated and has a clear efficiency. The drugs in this program are all standard treatment drugs for gastric cancer.
In 2020, JAMA Network Open and JAMA Oncology successively reported the application of FOLFIRINOX in the perioperative period of gastric cancer and the late-stage results of gastric cancer, and they obtained very amazing data respectively.
According to the results of CheckMate-649, the FDA approved Nivolumab combined chemotherapy for first-line treatment of advanced or metastatic gastric cancer, gastroesophageal junction cancer and
Sign in to get the eligibility rules as simple questions to take to your doctor.
📋 Eligibility rules (as published)
Inclusion Criteria:
1. At least 18 years of age, 75 years of age or less, no gender limitation;
2. Patients with untreated locally advanced resectable adenocarcinoma of the stomach or gastroesophageal junction, with clear pathological diagnosis;
3. According to RECIST 1.1, the efficacy evaluation standard for solid tumors, there were definite measurable and evaluable lesions, with spiral CT lesions ≥1cm；
4. Physical condition score KPS score 80-100 points ；
5. Able to receive systemic chemotherapy;
6. No obvious active bleeding;
7. No history of other malignancies, except cured carcinoma in situ of the cervix, basal carcinoma of the skin or squamous cell carcinoma;
8. Women of childbearing age had negative pregnancy test and had voluntarily taken effective and reliable contraceptive measures during the clinical trial；
9. Sign the informed consent form voluntarily；
Exclusion Criteria:
1. There are distant metastasis or local invasion of adjacent organs；
2. Tumor recurrence;
3. Suffered from or had previously suffered from autoimmune diseases;
4. Past organ transplantation or HIV patients;
5. Allergic to 5-fluorouracil, calcium leucoin, oxaliplatin, or irinotecan, or contraindications to 5-fluorouracil, calcium leucoin, oxaliplatin, or irinotecan exist;
6. Malignant secondary disease dating back to 5 years (exceptions: carcinoma in situ of the cervix, adequately treated basal cell carcinoma of the skin)；
7. Severe non-surgical complications or acute infections；
8. Peripheral polyneuropathy\>NCI Grad I；
9. Impaired blood system, liver and kidney function. The evaluation criteria are as follows:
Blood routine: white blood cells (WBC) \<3.0×109/L, neutrophils (ANC) \<1.5×109/L, platelets (PLT) \<100×109/L, hemoglobin (Hb) \<90g/L.
Liver and kidney function: total bilirubin (TBIL)\>1.5 times the upper limit of the normal value; urea nitrogen (BUN)\>1.5 times the upper limit of the normal value；Creatinine (Cr)\>1.5 times the upper limit of the normal value；Alanine aminotransferase and aspartate aminotransferase (ALT and AST)\> 3 times the upper limit of the normal value (without liver metastasis)；Alanine aminotransferase and aspartate aminotransferase (ALT and AST)\> 5 times the upper limit of the normal value (for liver metastases)；
10. Subjects with symptomatic brain metastases;
11. Subjects with obvious clinical manifestations of arrhythmia, myocardial ischemia, severe atrioventricular block, cardiac insufficiency, and severe valvular disease;
12. Subjects with severe bone marrow failure;
13. Psychotic subjects who are difficult to control；
14. Pregnant or lactating subjects;
15. Subjects whom the investigator considers inappropriate to participate in this trial；
16. Include in another clinical trial；
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