Advanced malignant solid tumor
Conditions
Interventions
treatment group:Revottack+PD-1
Sponsors
Affiliated Hospital of Xuzhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1) The age at the time of signing the informed consent is = 18 years old, regardless of gender; 2) Patients with advanced malignant solid tumor confirmed by histology or cytology; Failure in standard treatment (disease progression or intolerable treatment after treatment) and no effective treatment means, or no standard treatment scheme, or inability to obtain standard treatment due to objective conditions. 3) According to RECIST 1.1, there is at least one assessable tumor focus with the longest diameter = 10mm (if it is a malignant lymph node, the short diameter = 15mm is required); 4) ECOG physical strength score 0-2; 5) Full organ function: Blood system (no blood transfusion or hematopoietic stimulator treatment within 14 days) Absolute neutrophil count (ANC) = 1.5 × 109/L Platelet (PLT) = 75 × 109/L Hemoglobin (Hb) = 80g/L Lymphocyte absolute value (LYM) = 0.8 × 109/L liver function Total bilirubin (TBIL) = 1.5 × ULN Alanine aminotransferase (ALT) = 3 × ULN Patients with liver metastasis or liver cancer: = 5 × ULN Aspartate aminotransferase (AST) = 3 × ULN Patients with liver metastasis or liver cancer: = 5 × ULN renal function Creatinine clearance rate (Ccr) > 50ml/min/1.73m2 (calculated according to Cockcroft Gault formula) Coagulation function test Activated partial thromboplastin time (APTT) = 1.5 × ULN International normalized ratio (INR) = 1.5 × ULN 6) Eligible patients (male and female) with fertility must agree to work in Revottack ? Use reliable contraceptive methods (hormone or barrier method or abstinence) within 6 months after injection; The blood pregnancy test of female patients of childbearing age must be negative within 7 days before enrollment; 7) Subjects must give informed consent to the study before the study, and voluntarily sign a written informed consent form.
Exclusion criteria
Exclusion criteria: 1) Patients with active CNS metastasis and/or carcinomatous meningitis are known or found during screening. However, the following subjects are allowed to be included in the group: ? Patients with asymptomatic brain metastasis (that is, patients without progressive central nervous system symptoms caused by brain metastasis do not need to use corticosteroids) can participate. ? Subjects who had been treated and had stable brain metastases for at least 2 months had no evidence of new or expanded brain metastases. 2) He received chemotherapy, radiotherapy, biological therapy, endocrine therapy, targeted therapy, immunotherapy and other anti-tumor treatments within 2 weeks before the first use of the study drug; 3) Participated in other unlisted clinical studies within 4 weeks before the first use of the study drug; 4) Major organ surgery (excluding puncture biopsy) or significant trauma occurred within 4 weeks before the first use of the study drug, or major elective surgery required during the study period. 5) Patients who received systemic corticosteroids (prednisone>10mg/day or equivalent dose of the same drug) or other immunosuppressants within 14 days before the first use of the study drug; The following cases are excluded: local, eye, intra articular and intranasal corticosteroids are used for treatment; Short term use of corticosteroids for prevention and treatment; 6) Have received other oncolytic virus treatment within 8 weeks before the first use of the study drug; 7) Any vaccine was inoculated within 7 days before the first use of the study drug; 8) Antiviral drugs were used within 2 weeks before the first use of the study drug, and long-acting interferon was used within 4 weeks; 9) The adverse reaction of previous anti-tumor treatment has not recovered to = 1 level (except for the toxicity judged by the researcher as no safety risk, such as alopecia, hypothyroidism stabilized by hormone replacement therapy, etc.); 10) Uncontrolled active infection exists, which may seriously affect the efficacy and safety evaluation as judged by the researcher; 11) Have a history of immunodeficiency, including HIV antibody test positive; 12) Active hepatitis B (HBsAg positive and HBV DNA>the lower detection limit of the research center), or hepatitis C virus infection (anti HCV positive or HCV RNA positive), or syphilis infection; 13) Cardiovascular and cerebrovascular diseases shall conform to any of the following: a. Poor control of hypertension (systolic blood pressure = 150 mmHg or diastolic blood pressure = 100 mmHg); b. Cardiac function = Grade 2 congestive heart failure (NYHA classification); c. Arrhythmias requiring clinical intervention (including QTc = 450ms (male) and QTc = 470ms (female)); d. Serious arteriovenous thromboembolism events, including myocardial infarction, unstable angina, cerebrovascular accident or transient ischemic attack, pulmonary embolism, deep vein thrombosis or any other serious thromboembolism; 14) The third space effusion that cannot be controlled clinically is not suitable to be included in the group according to the judgment of the researcher; 15) Patients with active or ever suffered from autoimmune diseases that may recur (such as systemic lupus erythematosus, rheumatoid arthritis, vasculitis, etc.), except patients with clinically stable autoimmune thyroiditis; 16) Known alcohol or drug dependence; 17) Mental disorders or poor compliance; 18) Pregnant or lactating women; 19) The in
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adverse event/serious adverse event;the immunogenicity;the immunoreactivity;overall response rate;disease response rate;Overall Survival;Progression Free Survival;Pharmacokinetics characteristics;the viral shedding;Quality of life assessment; | — |
Countries
China
Contacts
Public Contacthanzhengxiang
Affiliated Hospital of Xuzhou Medical University
Outcome results
None listed