Extensive-Stage Small Cell Lung Cancer
Conditions
Interventions
experimental group:LDRT+Chemotherapy+Toripalimab+Tifcemalimab
Sponsors
West China Hospital of Sichuan University
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1. Age = 18 years, male or female; 2. Histologically or cytologically confirmed extensive stage small cell lung cancer; 3. Previously untreated extensive stage small cell lung cancer; 4. ECOG PS 0-1; 5. Measurable lesions according to RECIST 1.1, and measurable lesions can only be included in previously irradiated lesions if the lesion shows definite disease progression after radiotherapy; 6. Expected survival = 3 months; 7. Normal function of major organs, that is, meet the following criteria: neutrophils >= 1.5 × 10^9/L, platelet count >= 100 × 10^9/L, hemoglobin >= 90 g/L; serum creatinine = 50 mL/min; serum total bilirubin <= 1.5 × ULN, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) <= 2.5 × ULN; ALT and AST <= 5 × ULN in patients with liver metastases; international normalized ratio (INR) or prothrombin time (PT) <= 1.5 × ULN unless the subject is receiving anticoagulant therapy, activated partial thrombin time (aPTT) <= 1.5 × ULN unless the subject is receiving anticoagulant therapy; 8. Female subjects of childbearing potential, as well as male subjects with partners of childbearing potential, need to use a medically recognized contraceptive (such as an intrauterine device, contraceptive, or condom containing spermicide) during study treatment and for at least 4 months after the last use of study drug; 9. Voluntary participation in this study, signed informed consent, good compliance, with follow-up.
Exclusion criteria
Exclusion criteria: 1. Mixed SCLC and non-small cell lung cancer (NSCLC); 2. Symptomatic, untreated or progressive central nervous system (CNS) metastases; 3. Received any systemic anti-tumor therapy for ES-SCLC; 4. Previously received any immune checkpoint inhibitors, including but not limited to CTLA-4 inhibitors, PD-1/PD-L1 inhibitors, BTLA inhibitors; 5. Known hypersensitivity to the study drug or excipients, known serious allergic reactions to any monoclonal antibody; 6. Pulmonary artery invasion; 7. History of leptomeningeal disease; 8. Uncontrollable tumor-related pain; 9. Uncontrollable pleural effusion, pericardial effusion or ascites requiring repeated drainage; 10. Uncontrolled or symptomatic hypercalcemia; 11. Uncontrolled hypertension, history of hypertensive crisis or hypertensive encephalopathy; 12. Patients with active autoimmune diseases, autoimmune diseases or systemic use of steroids/immunosuppressive agents; 13. History of idiopathic pulmonary fibrosis, tissue pneumonia, drug-induced pneumonia, or idiopathic pneumonia, or evidence of active pneumonia on chest CT scan; 14. Active pulmonary tuberculosis, or patients with a history of active pulmonary tuberculosis infection within 1 year before enrollment, or patients with a history of active pulmonary tuberculosis infection more than 1 year ago but without regular treatment; 15. Known human immunodeficiency virus (HIV) infection, active hepatitis B or C patients; HBsAg positive patients may participate in this study if HBV DNA testing is < 500 IU/ml or if the lower limit of detection at the site. HCV antibody positive patients may participate in this study if HCV RNA detection is less than the lower limit of detection value at the site where they are located; 16. Patients with severe cardiovascular disease, such as New York Heart Association (NYHA) class 2 or higher heart failure, unstable angina pectoris, unstable arrhythmia, myocardial infarction or cerebrovascular accident within 6 months before enrollment; 17. Patients with other malignant tumors (except for non-melanoma skin basal cell carcinoma or squamous cell carcinoma, breast/cervical carcinoma in situ, superficial bladder cancer and other carcinoma in situ who have received radical treatment and have no evidence of disease recurrence) within 5 years before the start of treatment or at the same time; 18. According to the investigator 's judgment, the subject has other factors that may cause the subject to be forced to terminate the study halfway, such as having other serious diseases (including mental illness) requiring concomitant treatment, severely abnormal laboratory test values, and/or family or social factors that may affect the patient' s safety or collection of trial data.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safty; | — |
Secondary
| Measure | Time frame |
|---|---|
| Objective relief rate, ORR;Disease control rate, DCR;Duration of relief, DOR;Progression free survival, PFS;Overall survival, OS; | — |
Countries
China
Contacts
Public ContactLu You
West China Hospital of Sichuan University
Outcome results
None listed