A Single-arm, Open-label, Clinical Trial of Surufatinib/Serplulimab/Platinum/Etoposide in Neuroendocrine Carcinoma.

Prior treatment

• Received systemic immunostimulant therapy within 4 weeks before the first dose;
• Received any live vaccines or live attenuated vaccines within 4 weeks prior to the first dose or planned to be administered live vaccines or live attenuated vaccines during the study;

Other illness

• With known allergic reactions to the drugs in this study;
• Unable or unwilling to swallow Surufatinib or suffering from significant digestive system diseases that may interfere with absorption, metabolism, or excretion;
• With active ulcers, intestinal perforation, and intestinal obstruction;
• With active bleeding or bleeding tendency;
• With uncontrolled hypertension (systolic pressure \> 150 mmHg or diastolic pressure \> 100 mmHg) after the optimal medical treatment;
• Any active autoimmune disease requiring systemic treatment or with a history of autoimmune disease within 2 years, including but not limited to interstitial pneumonia, uveitis, inflammatory bowel disease, hepatitis, hypophysitis, vasculitis, systemic lupus erythematosus, etc. (Vitiligo, psoriasis, alopecia or Grave's disease without systemic treatment within the past 2 years, and type I diabetic patients who only need insulin replacement therapy can be included); with a history of primary immunodeficiency; patients only with positive autoimmune antibody need to confirm according to the investigator;
• Diagnosed with malignant tumors within 5 years before the first dose, excluding radically cured cutaneous basal cell carcinoma, cutaneous squamous cell carcinoma, and/or radically resected carcinoma in situ;
• Presence of severe infection in the active phase or with poor clinical control;
  • With known history of human immunodeficiency virus (HIV) infection or confirmed with positive immune test results;
  • Acute or chronic active hepatitis B or C infection; hepatitis B virus (HBV) DNA \> 2000 IU/mL or 104 copies/mL; hepatitis C virus (HCV) RNA \> 103 copies/mL; or other hepatitis, liver cirrhosis.

Lab values

• With clinically significant or uncontrolled heart diseases, including unstable angina, acute myocardial infarction within 6 months before the first dose, grade III/IV congestive heart failure (New York Heart Association), and uncontrolled arrhythmia (subjects with pacemakers or with atrial fibrillation but well controlled heart rate are allowed); With ECG changes or medical history considered clinically significant by the investigator; QTc interval \> 450 ms for male or \> 470 ms for female at screening;
• The investigator confirms that the patients has any clinical or laboratory abnormalities who are not suitable for participating in this clinical study.

Other

• Neuroendocrine carcinoma of the lung;
• Urine protein ≥ ++ and the amount of urine protein in 24 hours \>1.0g;
• Pleural effusion, ascites, or pericardial effusion with obvious clinical symptoms that require drainage;
• Symptomatic brain metastases (confirmed or suspected)

• Written informed consent;
• With histologically or cytologically confirmed extra-pulmonary neuroendocrine carcinoma (including mixed neuroendocrine or non-neuroendocrine tumors \[at least 30% neuroendocrine carcinoma component\]);
• Previously untreated with systemic therapy;
• age ≥18 years;
• Have at least one measurable lesion according to RECIST v1.1;
• ECOG performance status: 0-1;
• Expected survival time \> 3 months;
• For evidence of sufficient organ functions, the subjects shall meet the following laboratory parameters: 1) Absolute neutrophil count (ANC) ≥ 1.5 x 109/L without use of granulocyte colony stimulating factor in recent 14 days; 2) Platelet count ≥ 100 × 109/L without blood transfusion in recent 14 days; 3) Hemoglobin \> 9 g/dL without blood transfusion or erythropoietin use in recent 14 days; 4) Total bilirubin ≤ 1.5 × upper limit of normal (ULN); or total bilirubin \> ULN, direct bilirubin ≤ ULN; 5) Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN (ALT or AST ≤ 5 × ULN for patients with liver metastasis); 6) Blood creatinine ≤ 1.5 × ULN and creatinine clearance (calculated by Cockcroft- Gault formula) ≥ 50 mL/min;
• Women of childbearing potential need to use at least one medically approved contraceptive measure (such as intrauterine device, contraceptive pill or condom) during the study treatment and within 180 days after the end of the study treatment; Before the first dose, serum HCG examination must be negative; and women must be non-lactating.