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临床试验/NCT01130961
NCT01130961已完成不适用

Management of Advanced Non-Small Cell Lung Cancer and Clinical Outcomes in Patients Who Received Gefitinib (IRESSA) in Tertiary Care Setting in Thailand

AstraZeneca1 个研究点 分布在 1 个国家目标入组 104 人开始时间: 2009年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
AstraZeneca
入组人数
104
试验地点
1
主要终点
Progression-free survival

研究概览

简要总结

The purpose of this study is to determine progression-free survival of lung cancer patients who received gefitinib in clinical practice in Thailand.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Diagnosed as having lung cancer based on histological/cytological findings
  • Admitted to the hospital between January 2004 and December 2008
  • Treated with gefitinib for at least 3 months

排除标准

  • Involvement in the planning and/or conduct of the study
  • Participation in another clinical study during the last 3 months

结局指标

主要结局

Progression-free survival

时间窗: median time from the first date of treatment until date of disease progression during Jan 2004- Dec 2008 or 5 years approx.

次要结局

  • Time to maximum response(Median time from the first date of treatment until the date that the disease can be maximum controlled during Jan 2004- Dec 2008 or 5 years approx.)
  • Overall survival(time from the first date of treatment until date of patients dead during Jan 2004- Dec 2008 or 5 years approx.)
  • Prevalence of EGFR & KRAS mutation from laboratory result(During Jan 2004- Dec 2008 or 5 years approx.)

研究者

发起方
AstraZeneca
申办方类型
Industry

研究点 (1)

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