SBRT Sequential Surufatinib Combined With Immunotherapy for Biliary Tract Carcinoma

Exclusion Criteria

• •The study proposal shall be excluded if any of the following criteria are met:
• •1. Have received any antitumor therapy in the past (except simple surgical resection);
• •2. The tumor directly invades the stomach, small intestine or colon;
• •3. The maximum diameter of the lesion exceeds 10cm, or the satellite lesion does not meet the above definition criteria;
• •4. Have had other malignancies within the past 5 years, except basal cell or squamous cell carcinoma of the skin after radical surgery, or carcinoma in situ of the cervix;
• •5. There are extra-hepatic metastases (excluding local regional lymph nodes);
• •6. Normal liver volume is less than 1000cc;
• •7. The patient currently has hypertension that cannot be controlled by drugs, as follows: systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg;
• •8. Urine routine indicated urinary protein ≥2+, and 24-hour urinary protein volume \>1.0g;
• •9. Patients whose tumors are judged by the investigators to be at high risk of invading vital blood vessels and causing fatal massive bleeding during the follow-up study;
• •10. Patients with evidence or history of significant bleeding tendency within 3 months prior to enrollment (bleeding within 3 months\> 30 mL, hematemesis, stool, stool blood), hemoptysis (within 4 weeks \> 5 mL fresh blood); Patients with a history of hereditary or acquired bleeding or coagulation disorders have clinically significant bleeding symptoms or definite bleeding tendencies within 3 months, such as gastrointestinal bleeding and hemorrhagic gastric ulcers;
• •11. Clinically significant cardiovascular disease, including but not limited to acute myocardial infarction, severe/unstable angina pectoris, or coronary artery bypass grafting within 6 months prior to enrollment; New York Heart Association (NYHA) Grades for Congestive Heart Failure \>Level 2; Ventricular arrhythmias requiring medical treatment; Electrocardiogram (ECG) showed QTC interval ≥480 ms.
• •12. Active or uncontrolled severe infection (≥CTCAE grade 2 infection);
• •13. Women who are pregnant (positive pregnancy test before medication) or breastfeeding;
• •14. Any other medical condition, clinically significant metabolic abnormality, physical abnormality or laboratory abnormality, in which, in the investigator's judgment, there is reason to suspect that the patient has a medical condition or condition that is not suitable for the use of the investigational drug (such as having seizures and requiring treatment), or that would affect the interpretation of the study results or place the patient at high risk;
• •15. Known human immunodeficiency virus (HIV) infection; Known history of clinically significant liver disease, including viral hepatitis \[Known hepatitis B virus (HBV) carriers must rule out active HBV infection, i.e., positive HBV DNA (\>1×104 copies /mL or \>2000 IU/ml); known hepatitis C virus infection (HCV) and HCV RNA positive (\>1×103 copies /mL), or other hepatitis, cirrhosis\];
• •16. The presence of any active, known or suspected autoimmune disease (including but not limited to: myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, enteritis, multiple sclerosis, vasculitis, glomerulonephritis, uveitis, pituitaries, hyperthyroidism, etc.);
• •17. Allergy or suspected allergy to the investigational drug or similar drugs; According to the investigators' judgment, the patients had other factors that might affect the study results or lead to the forced termination of the study, such as alcoholism, drug abuse, other serious diseases (including mental illness) requiring combined treatment, serious laboratory abnormalities, and family or social factors that would affect the safety of the patients.