Neoadjuvant PD-1 Monoclonal Antibody in Cisplatin-ineligible High Risk Upper Tract Urothelial Carcinoma

Prior treatment

• 1\. Patients who have received prior therapy of an anti-PD-1, anti-PD-L1, or anti-PD-L2 antibody;
• 3\. Patients who have received other systems for anti-tumor treatment (e. g., Steroid therapy, immunotherapy) within 4 weeks or enrolled in other clinical trials;
• 8\. Patients who have received a live vaccine within 30 days prior to the first dose of trial treatment;
• 9\. Patients who have received prior radiation therapy to the bladder;
• 11.Patients who have received allogeneic hematopoietic stem cell transplantation or solid organ transplantation;

Other illness

• 2\. Patients who are allergic to monoclonal antibodies or any of its excipients;
• 5\. Patients who have a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies);
• 6\. Patients who have known active Hepatitis B or Hepatitis C;
• 7\. Patients who have active autoimmune disease that has required systemic treatment in the past 2 years;
• 10.Patients who have muscle invasive bladder cancer;
• 12.Patients who have a history of substance abuse or with a history of mental disorders;
• 13.Patients who had other malignant tumors in the past five years that have not recovered except for curable tumors that have been cured including basal or squamous skin cancer, localized carcinoma in situ of the cervix or the breast and low-risk prostate cancer, etc.
• 14.Patients who have active tuberculosis;
• 15.Patients who have other serious and uncontrollable accompanying diseases that may affect compliance or interfere with the interpretation of results including active opportunistic infections or advanced (severe) infections, uncontrollable diabetes, cardiovascular disease (grade III or IV heart failure defined by the New York Heart Association classification, II degree atrioventricular block and above, myocardial infarction in the past 6 months, unstable arrhythmia or instability angina, cerebral infarction within 3 months, etc.) or lung disease (interstitial pneumonia, history of obstructive lung disease and symptomatic bronchospasm);

Other

• 4\. Patients who are pregnant or breastfeeding, or expecting to conceive;

• 1\. had non-metastatic high risk UTUC and planed to receive surgery(defined as high grade UTUC either by endoscopic biopsy or urinary cytology and/or any invasive aspect on radiological examination and/or hydronephrosis );
• 2\. were ineligible for cisplatin-based chemotherapy(defined as meeting at least one of the following criteria: Eastern Cooperative Oncology Group \[ECOG\] performance status 2, creatinine clearance 30-60 mL/min, grade ≥2 audiometric hearing loss, grade ≥2 peripheral neuropathy, or New York Heart Association Class III heart failure);
• 3\. had not received any systemic anti-tumor therapy;
• 4\. Adequate organ function defined by study-specified laboratory tests; Hemoglobin ≥90 g/L; Hematological Absolute neutrophil count (ANC) ≥1.5×109 /L; Platelets ≥100×109 /L
• 5\. No functional organic disease: T-BIL≤1.5×upper limit of normal (ULN); ALT andAST≤2.5×ULN; Serum creatinine≤2×ULN; endogenous creatinine clearance rate\>30ml/min
• 6\. Agree to comply with scheduled visits, treatment plans, lab tests and any other required study procedures;