Safety & Efficacy of DC Vaccine and TMZ for the Treatment of Newly-diagnosed Glioblastoma After Surgery

Exclusion Criteria

• •1. Subjects with any other active malignancy;
• •2. Subjects received the placement of Carmustine implants within 6 months before the inclusion;
• •3. Subjects with active HBC, HCV or HIV infection;
• •4. Subjects with grade 2 -3 hypertension or uncontrolled hypertension;
• •5. Subjects with severe cardio- or cerebro- vascular diseases such as coronary heart disease, angina pectoris, myocardial infarction, arrhythmia, cerebral thrombosis, cerebral hemorrhage, etc.;
• •6. Subjects with uncontrolled autoimmune diseases such as hemolytic anemia, psoriasis and rheumatoid arthritis, etc.;
• •7. Subjects with severe or uncontrolled psychiatric diseases or condition that could increase adverse events or interfere the evaluation of outcomes;
• •8. Subjects receiving immunosuppressants after organ transplantation;
• •9. Within four weeks before the DC vaccinations, subjects receiving systemic administration of steroids with dosage more than 10mg/d prednisone or the equivalent doses of other steroids ( not including inhaled corticosteroid);
• •10. Subjects with unstable pulmonary embolism, deep venous embolism, or other major arterial and venous thromboembolic events that occur within 30 days before the enrollment; receiving ongoing anticoagulant therapy;
• •11. Subjects in pregnancy or breastfeeding, or those who plan to become pregnant during treatment or within 2 months after the end of treatment;
• •12. Within the 14 days before enrollment, subjects with active infections or uncontrolled infections that require systemic antibiotic treatment (except for simple urinary tract infections or upper respiratory tract infections);
• •13. Subjects who have received other vaccine therapies or gene-modified cell therapy before enrollment;
• •14. Subjects with number of the predicted neoantigen peptides less than 5;
• •15. Subjects with other conditions that would interfere trial participation at the investigator's discretion;
• •16. Subjects with medical conditions that affect signing the written informed consent or complying with the research procedures; or patients who are unwilling or unable to comply with the research procedures;
• •17. Subjects who participated or are participating in other clinical trials within 4 weeks before enrollment.