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临床试验/KCT0005952
KCT0005952招募中未知

Real-world outcomes of brigatinib compared to alectinib as a second-line therapy after crizotinib in advanced anaplastic lymphoma kinase positive non-small cell lung cancer patients

Asan Medical Center0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational Study

入排标准

年龄范围
18?(Year) 至 0No Limit(—)
性别
All

入选标准

  • 1. Male or female adult patients aged 18 years old and above
  • 2. Patients who were diagnosed as locally advanced or metastatic NSCLC from Jan 2011
  • 3. Patients who were diagnosed as histologically or cytologically ALK positive adenocarcinoma
  • 4. Patients who initiated crizotinib as a first-line therapy and experienced disease progression
  • (definitive CCRT, neoadjuvant or adjuvant chemotherapy prior to crizotinib are allowed)
  • 5. Patients who were treated with crizotinib for at least 84 days
  • 6. Patients who are eligible to evaluate response to brigatinib or alectinib
  • 7. Patients who provide written informed consent for the study

排除标准

  • 1. Patients who were treated with ALK inhibitors other than alectinib or brigatinib after crizotinib failure
  • 2. Patients who stopped a first-line crizotinib treatment for other than disease progression
  • 3. Patients who received chemotherapy in between crizotinib and 2nd line ALK inhibitor
  • 4. Patients whose medical records are not available for review

研究者

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