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临床试验/NCT01494558
NCT01494558已完成2 期

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

Chinese Academy of Medical Sciences0 个研究点目标入组 200 人开始时间: 2007年5月最近更新:
适应症

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

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

申办方类型
Other
责任方
Principal Investigator
主要研究者

Luhua Wang

Chairman of Thoracic Group, Clinical Professor, Radiation Oncology Department, Cancer Hospital&Institute

Chinese Academy of Medical Sciences

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