Phase 3 Study of Etoposide, Cisplatin, and Radiotherapy Versus Paclitaxel, Carboplatin and Radiotherapy in Patients With Unresectable Locally Advanced, Stage III Non-Small Cell Lung Cancer
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 200
- 主要终点
- Overall Survival
研究概览
简要总结
Cisplatin-based combination chemotherapy given concurrently with radiotherapy is the standard of care for patients with inoperable stage III NSCLC. The most common chemotherapeutic agents used concurrently with radiotherapy have been vinorelbine, vinblastine, and etoposide in conjunction with cisplatin or weekly paclitaxel and carboplatin. No randomized phase III trials of concurrent chemoradiotherapy have shown the superiority of one chemotherapy regimen over another. The clinical trial is to compare radiotherapy concurrently with PE (etoposide and cisplatin) and PC (paclitaxel and carbplatin) for local advanced NSCLC (stage IIIA/IIIB). It is a randomized, multicenter, open labeled phase III clinical trial. All patients receive conformal radiotherapy or intensity modulated radiotherapy with conventional fraction. The chemotherapy regimens are PE (etoposide 50mg/m2 d1-5, 29-33 and cisplatin 50mg/m2 d1,8,29 and 36 29-33 ) and PC (paclitaxel 45mg/m2 weekly over 1hour and carbplatin AUC =2mg/mL/min over 30min weekly). The primary purpose is to evaluate objective response rate, complications, progression-free survival, overall survival. The second purpose is to evaluate quality of life and cost.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Inoperable stage IIIA/IIIB NSCLC proved by pathology or cytology
- •Age 18 to 75, ECOG ≤ 2, lose weight <10% during 6 months
- •No serious diseases of important organs
- •Chest CT in recently 4 weeks
- •No other tumor disease except stage I cervical cancer or cutaneous basal cell carcinoma
- •Sign consent
- •Measurable lesion
排除标准
- •Pretreatment radiotherapy or chemotherapy
- •Pregnant or lactation woman
- •Serious diseases (include uncontrolled diabetes and infection) of important organs
- •Join in other clinical trial
结局指标
主要结局
Overall Survival
时间窗: 2 years
次要结局
- Progression Free Survival(2 years)
研究者
Luhua Wang
Chairman of Thoracic Group, Clinical Professor, Radiation Oncology Department, Cancer Hospital&Institute
Chinese Academy of Medical Sciences
