Camrelizumab Combined With Apatinib in the Treatment of Patients With Advanced Gastric Cancer and Colorectal Cancer

Inclusion Criteria: * Age 18 - 75 years； * Patients with histologically or cytologically confirmed advanced or metastatic gastric cancer and colorectal cancer. * Patients who had previously progressed after receiving standard second-line advanced treatment； * Patients with at least one evaluable or measurable lesions as per RECIST version 1.1 （CT scan length and diameter of tumor lesion≥10mm，CT scan of lymph node lesion was short diameter≥15mm，scan slice thickness 5mm；） * ECOG performance status (PS) 0 - 2； * Life expectancy of at least 3 months； * Patients with adequate organ function at the time of enrollment as defined below: 1. Blood routine examination standard：（without blood transfusion within 14 days before enrollment） 1. Hb ≥90g/L， 2. WBC≥3.0×109/L 3. ANC ≥ 1.5×109/L， 4. PLT ≥ 80×109/L； 2. Biochemical examination shall meet the following standards： 1. BIL \<1.5 times the upper limit of normal（ULN）， 2. ALT and aspartate aminotransferase (AST) \<2.5×upper limit of normal (ULN)，If liver metastasis is present，ALT and AST\<5ULN ； 3. Serum creatinine Cr≤1ULN，Serum creatinine \>50ml/min（Cockcroft-Gault math） * Women of childbearing age in the serum or urine pregnancy test is negative within 7 days prior to study enrollment and must be Non-lactating patients，and agree to use contraceptives (such as intrauterine devices, contraceptives or condoms) during the study period and within 8 months after the end of the study； males should agree to patients who must use contraception during the study period and within 8 months after the end of the study period * Subjects voluntarily joined the study, signed informed consent, good compliance, and followed up; Exclusion Criteria: * Except for other malignant tumors, basal cell carcinoma of the skin and cervical cancer in situ in the past 5 years； * Patients who have undergone systemic chemotherapy, radiotherapy, surgery, hormone therapy, or immunotherapy \<2 weeks before enrollment； * With severe heart, liver, lung and kidney disease；Significant neurological or psychiatric disorders；Patients with partial or complete gastrointestinal obstruction； * Patients with a large amount of pleural effusion or ascites requiring drainage； * Patients with symptomatic brain metastasis； * Patients with hypertension that is difficult to control (systolic blood pressure ≥140 mmHg and diastolic blood pressure ≥90 mmHg) despite treatment with several hypotensive agents; Patients with acute coronary syndrome (including myocardial infarction and unstable angina), and with a history of coronary angioplasty or stent placement performed within 6 months before enrollment；Patients with acute coronary syndrome（included QTc male\>450ms，female\>470ms）and cardiac dysfunction； * Women who are pregnant or breastfeeding； * Patients with concurrent autoimmune disease, or a history of chronic or recurrent autoimmune disease; * Patients with concurrent autoimmune disease, or a history of chronic or recurrent autoimmune disease: included HIV positive or a history of organ transplantation and allogeneic bone marrow transplantation; * Patients with interstitial lung disease with symptoms or signs of activity； * Patients with a risk of gastrointestinal bleeding may not be enrolled, including the following: (1) active digestive ulcer lesions and fecal occult blood (++); (2) nausea and hematemesis within 2 months Medical history. Simple fecal occult blood (+) is not an exclusion criterion；Coagulation abnormalities （INR\>1.5、APTT\>1.5ULN）； * Urine protein ≥ ++ or confirmed 24 hour urine protein quantitation； * Patients with non-healing wound, non-healing ulcer, or non-healing bone fracture; * Patients with a seizure disorder who require pharmacotherapy； * Patients with a history of hypersensitivity to any of the study drugs, similar drugs, or excipients； * The investigator believes that there are any conditions that may damage the subject or result in the subject being unable to meet or perform the research request; * participated in other clinical studies before and during treatment；