跳至主要内容
临床试验/NCT00190476
NCT00190476终止3 期

Randomized Controlled Trial Comparing Docetaxel-cisplatin Combination With Docetaxel Alone in Elderly Patients With Advanced Non-small-cell Lung Cancer(JCOG0207)

Japan Clinical Oncology Group29 个研究点 分布在 1 个国家目标入组 230 人开始时间: 2003年4月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
230
试验地点
29
主要终点
overall survival

研究概览

简要总结

To evaluate the efficacy of docetaxel-cisplatin combination in comparison to docetaxel alone for elderly patients with advanced non-small-cell lung cancer.

详细描述

The Elderly Lung Cancer Vinorelbine Italian Study demonstrated the first evidence of the utility of chemotherapy in elderly patients with advanced non-small-cell lung cancer (NSCLC). In a large randomized trial, gemcitabine and vinorelbine failed to show any advantage over either agent alone. With the current evidence, single agent chemotherapy with a third-generation drug can be considered a recommended option for elderly patients with advanced NSCLC. A Japanese phase I/II study showed the activity (overall response rate 52%, median survival 12.4 months) and tolerability of weekly docetaxel/ cisplatin combination in patients older than age 75 years. There have been no randomized prospective trials dedicated to elderly NSCLC patients to evaluate tolerability and efficacy of platinum-based combination.

Comparison: Single-agent weekly docetaxel versus weekly regimen of docetaxel-cisplatin combination for elderly advanced NSCLC.

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
70 Years 至 —(Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •histologically or cytologically proven non-small-cell lung cancer
  • •stage IV, or stage III disease ineligible for definitive radiotherapy
  • •70 years or older
  • •ECOG PS 0-1
  • •Ineligible for standard platinum(bolus infusion)-containing combination chemotherapy
  • •No prior chemotherapy(containing gefitinib) for non-small cell lung cancer or other neoplasms
  • •No prior surgery within 4 weeks before enrollment
  • •No prior radiotherapy for primary tumor
  • •No prior radiotherapy for metastatic lesions within 2 weeks before enrollment
  • •Adequate organ function
  • •Signed informed consent

排除标准

  • •Symptomatic brain metastasis
  • •Active another neoplasms
  • •Severe SVC syndrome
  • •Massive pericardial, pleural effusion, or ascites
  • •Bone metastasis emergent for palliative radiotherapy or surgery
  • •Uncontrollable systemic hypertension
  • •Heart failure, Unstable angina, Myocardial infarction within 6 months
  • •Uncontrollable diabetes
  • •Active infection
  • •Interstitial pneumonia/ Pulmonary fibrosis
  • •Hypersensitivity for polysorbate 80
  • •Systemic administration of corticosteroids

结局指标

主要结局

overall survival

次要结局

  • Progression-free survival
  • Response rate
  • Symptom score
  • Toxicity

研究者

申办方类型
Other

研究点 (29)

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