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临床试验/NCT00540241
NCT00540241已完成不适用

Performance Status and Influencing Factors During Second-Line Treatment With Pemetrexed in Patients With Stage III/IVNon Small Cell Lung Cancer

Eli Lilly and Company1 个研究点 分布在 1 个国家目标入组 542 人开始时间: 2007年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
542
试验地点
1

研究概览

简要总结

The primary research objective of this observational study in pretreated patients with NSCLC of Stage IIIa/b or Stage IV is to evaluate patients' Karnofsky Index (KI) after the second cycle of second-line treatment with single agent pemetrexed in a real life setting, and to evaluate factors potentially influencing performance status in terms of KI, i.e. frequency of use of concomitant medications, in particular analgesics, folic acid, Vitamin B12, antiemetics, and medications against diarrhea; as documented in patient diary (days of use per week) and by the physicians.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Are 18 years of age or older
  • Have NSCLC, Stage IIIa/b or IV, that is not amenable to curative therapy
  • Have had one prior chemotherapy regimen with cytotoxic agents for the treatment of NSCLC (patients with adjuvant and neoadjuvant regimens are also eligible. However, patients with one prior cytotoxic chemotherapy followed by a targeted agent such as erlotinib are not eligible because the targeted agent would be regarded as second-line treatment)
  • Are initiating second-line of treatment for NSCLC with pemetrexed
  • Have been fully informed and have given written consent for the use of their data.

排除标准

  • Have received any prior treatment with pemetrexed
  • Are participating in a study including administration of any investigational drug or procedure at entry into this study

研究组 & 干预措施

Second-line pemetrexed treatment in NSCLC

Patients with NSCLC who will start second-line treatment with pemetrexed.

干预措施: Pemetrexed (Drug)

研究者

申办方类型
Industry

研究点 (1)

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