Nimotuzumab Combined With Neoadjuvant Chemotherapy (TPF) in the Treatment of Resectable Locally Advanced Head and Neck Squamous Cell Carcinoma
试验速览
- 阶段
- 2 期
- 发起方
- 入组人数
- 55
- 主要终点
- Objective Response Rate (ORR)
研究概览
简要总结
This study is a prospective, open-label, single-arm study. The trial will be divided into 3 phases: screening/baseline, treatment and follow-up. To initially explore the efficacy and safety of nimotuzumab combined with neoadjuvant chemotherapy (TPF regimen) in the treatment of resectable locally advanced head and neck tumors. Targeted therapy: Nimotuzumab injection 400 mg, once on the 1st day and once on the 21st day, for a total of 2 times. It should be administered by intravenous infusion 1 hour before chemotherapy, and the administration process should last for more than 60 minutes. Chemotherapy (TPF regimen): nab-paclitaxel 175mg/m2, on the 1st day; nedaplatin 100mg/m2, on the 1st day; oral administration of Sigirone on the 1st-14th day, 2/day; a treatment cycle of 21 days, a total of 2 a treatment cycle. After two cycles of chemotherapy, all patients underwent radical surgery according to whether the throat could be preserved and the patient's own wishes. The primary endpoint of the study is the tumor objective response rate (ORR), and the secondary endpoints are the primary tumor pathological complete response (pCR) rate, organ preservation rate, 1-year overall survival (OS) rate, and 1-year disease-free survival (DFS) rate. , quality of life, safety evaluation.
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 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •18-80 years old, including 18 and 80 years old;
- •Resectable stage III to IVa head and neck squamous cell carcinoma (including oropharyngeal carcinoma, laryngeal carcinoma and hypopharyngeal carcinoma) was confirmed by histopathology or cytology by MRI imaging;
- •ECOG PS score 0-2;
- •Histopathological immunohistochemical test indicated positive EGFR expression
- •Histopathological immunohistochemical tests were P16 negative and EBER negative
- •Lymph nodes have signs of extraperitoneal invasion (MRI, CT or pathology)
- •At least one measurable lesion according to RECIST 1.1 evaluation criteria;
- •Expected survival time ≥6 months;
- •Hematologic indexes were basically normal: white blood cell count ≥4×109/L; Neutrophil absolute count ≥1.5×109/L; Platelet ≥100×109/L; Hemoglobin ≥90 g/L;
- •Normal renal function: serum creatinine ≤1.5×ULN or creatinine clearance (CrCl)> 60 mL/min(Cockcroft-Gault formula was used):
- •Female CrCl=(140- age)× body weight (kg)× 0.85 / (72×Scr mg/ dL) Male CrCl=(140- age)× body weight (kg)× 1.00 / (72×Scr mg/dl)
- •Normal liver function: serum total bilirubin ≤1.5×ULN; Aspartate aminotransferase (AST) ≤2.5×ULN; Alanine aminotransferase (ALT) ≤2.5×ULN
- •Female patients must have a negative urinary pregnancy test prior to study initiation (not available in patients with bilateral oophorectomy and/or hysterectomy or postmenopausal patients)
- •Signed written informed consent.
排除标准
- •Received PD-1 inhibitor, EGFR mab, EGFR-TKI and anti-angiogenic drugs within 4 weeks before enrollment;
- •Participating in other interventional clinical trials within 30 days prior to screening;
- •History of other malignant tumors (except cured basal cell carcinoma of the skin)
- •there are serious and poorly controlled concurrent diseases (such as heart failure, diabetes, hypertension, liver failure, renal failure, thyroid disease, mental illness, etc.);
- •known to be infected with HIV or active viral hepatitis or tuberculosis;
- •Major surgical or planned surgery within 30 days of the first administration of the investigational drug;
- •Allergic to drugs or ingredients used in the program;
- •Women who are pregnant (as confirmed by blood or urine HCG testing) or who are lactating, or subjects of childbearing age are unwilling or unable to use effective contraceptive methods (for both male and female subjects) until at least 6 months after the last trial treatment;
- •The researcher considers it inappropriate to participate in the study;
- •Unwilling to participate in the study or unable to sign the informed consent.
研究组 & 干预措施
study arm
The study arm received nimotuzumab (400mg, every three weeks, for 2 weeks) combined with TPF chemotherapy
干预措施: Nimotuzumab Combined With Neoadjuvant Chemotherapy (Drug)
结局指标
主要结局
Objective Response Rate (ORR)
时间窗: 1 year
次要结局
- Incidence of treatment-emergent adverse events(1 year)
- Primary pathological complete response rate (pCR)(1 year)
- R0 resection rate(1 year)
- Organ retention rate(1 year)
- Overall survival (OS)(1 year)
- Disease free survival (DFS)(1 year)
- Quality of life assessed by EORTC QLQ-H&N35(1 year)
- The change of tumor related markers(1 year)