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临床试验/NCT01333007
NCT01333007已完成不适用

A Cohort Study of First-line Treatment of Patients With Unresectable Advanced (Stage IIIB), Metastatic (Stage IV) or Recurrent Non Squamous Non-small Cell Lung Cancer (NSCLC), Starting a Treatment With Bevacizumab (Avastin®) in Combination With Chemotherapy.

Hoffmann-La Roche0 个研究点目标入组 423 人开始时间: 2010年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
423
主要终点
Progression-free survival

研究概览

简要总结

This observational study will evaluate modality, efficacy and safety of Avastin (bevacizumab) as first-line treatment in combination with chemotherapy in patients with inoperable advanced, metastatic or recurrent non-squamous non-small cell lung cancer in clinical practice. Data will be collected for each patient for 18 months from initiation of Avastin therapy.

研究设计

研究类型
Observational
观察模型
Cohort
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

  • Adult patients, >/= 18 years of age
  • Inoperable advanced, metastatic or recurrent non-squamous non-small cell lung cancer (NSCLC)
  • Treating physician's decision to initiate first-line Avastin treatment

排除标准

  • Participation in a clinical trial evaluating anti-cancer therapies

结局指标

主要结局

Progression-free survival

时间窗: 18 months

次要结局

  • Overall survival(18 months)
  • Quality of Life: Functional Assessment of Cancer Therapy-Lung (FACT-L) questionnaire(18 months)
  • Clinical (diagnosis, therapies, comorbidity) and demographic characteristics of patients initiated on Avastin treatment(18 months)
  • Treatment of non-squamous NSCLC in clinical practice(18 months)
  • Modality of treatment with Avastin (dose, duration, associated chemotherapy)(18 months)
  • Safety: Incidence of adverse events(18 months)

研究者

申办方类型
Industry
责任方
Sponsor

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