NCT05350891招募中2 期
A Prospective, Single-arm, Multicenter Clinical Study of Transnasal Endoscopic Surgery Combined With Adjuvant Immunotherapy for Recurrent Nasopharyngeal Carcinoma
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 77
- 试验地点
- 8
- 主要终点
- progression free survival
研究概览
简要总结
A Prospective, Single-arm, Multicenter Clinical Study of Transnasal Endoscopic Surgery Combined With Adjuvant Immunotherapy for Recurrent Nasopharyngeal Carcinoma
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Pathology or radiography confirmed recurrent nasopharyngeal carcinoma.
- •AJCC rT1-T4 which can be surgically removed.
- •Age ≥18 years old.
- •Informed consent signed.
- •With or without lymph node metastasis, which can be surgically removed.
- •No distant metastasis.
- •≥6 months from the end of initial radiotherapy to recurrence.
- •Sufficient organ function a)Hematology: white blood cells ≥3.0 x 109/L, absolute neutrophil count ≥1.5x 109/L, hemoglobin ≥80 g/L, platelets ≥100 x 109/L. b) Liver function: bilirubin ≤ 1.5 times the upper limit of normal (ULN), AST and ALT ≤ 3 times the ULN c) International normalized ratio (INR) or prothrombin time (PT) or activated partial thromboplastin time (aPTT) ≤ 1.5 times ULN. d) Renal function: serum creatinine ≤ 1.5 times ULN.
- •ECOG score 0-
- •general physical condition can tolerate general anesthesia surgery, chemotherapy, and immunotherapy.
排除标准
- •Evidence of distant metastasis or leptomeningel disease (LMD).
- •Have received radioactive seed implantation in the treatment area.
- •Suffer from uncontrolled disease which could interfere with treatment.
- •Suffered from another malignant tumor or multiple primary tumors at the same time within 5 years (excluding fully treated basal cell or squamous cell skin cancer, cervical cancer in situ, etc.).
- •The patient has surgical contraindications: such as severe cardiopulmonary disease, coagulation dysfunction and so on.
- •The patients have autoimmune diseases.
- •The patient is using immunosuppressive agents or systemic glucocorticoid to achieve the purpose of immunosuppression (dose>10mg/day prednisone or other), and continues to use it within 2 weeks before the first administration.
- •Severe allergic reaction to other monoclonal antibodies.
- •Previously received PD-1 monoclonal antibody, CTLA-4 monoclonal antibody (or any other antibody that acts on T cell co-stimulation or checkpoint pathway) treatment.
- •Live vaccines have been inoculated within 4 weeks before the first administration or during the study period.
- •The patient has any situation that may hinder study compliance or the safety during the study period.
- •Existence of serious neurological or psychiatric diseases, such as dementia and seizures.
- •Uncontrolled active infection.
- •Pregnant or breastfeeding women.
- •Those who have no personal freedom and independent capacity for civil conduct.
- •There are other situations that are not suitable for entry into the study.
结局指标
主要结局
progression free survival
时间窗: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first,through study completion,up to 2 years.
2 year progression free survival
次要结局
- Overall survival(From date of enrollment until the date of death from any cause,through study completion,up to 2 years.)
研究者
Hongmeng Yu
Principal Investigator, Professor
Eye & ENT Hospital of Fudan University
研究点 (8)
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