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临床试验/NCT01951469
NCT01951469Unknown3 期

Multicenter Phase III Study of Gefitinib Mono-therapy or Gefitinib Combined With Chemotherapy in Patients With Brain Metastases From Non-small Cell Lung Cancer Harboring EGFR Mutation

Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2016年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
发起方
入组人数
160
试验地点
1
主要终点
iPFS(intracranial progression free survival

研究概览

简要总结

This is a multi-center phase III randomized controlled study to assess the efficacy of Gefitinib alone and Gefitinib combination with Pemetrexed/platinum on patients with brain metastasis from non-small cell lung cancer(NSCLC) harboring EGFR mutation type by intracranial PFS(iPFS),also PFS ,DCR and OS.The side effect is evaluated as well.

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
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient who was confirmed stage IV NSCLC with EGFR activating mutation and brain metastases by pathologic histology or cytology
  • Patients who had never received therapy (including chemotherapy,WBRT,EGFR-TKI and EGFR monoclonal antibody) after diagnosed brain metastases
  • Patients had at least three metastatic lesions in brain, or patients with 1-2 intracranial lesions who were not suitable for brain radiotherapy, or patients with 1-2 intracranial lesions who refused brain radiotherapy, at least one intracranial lesion with the longest diameter of >5 mm
  • Adult patients (≥ 18 years and ≤75 years). ECOG Performance Status 0 or 1 Life expectancy of at least 12 weeks.,Haemoglobin ³ 10.0 g/dl, Absolute neutrophil count (ANC) ³1.5 x 109/L, platelets ³ 100 x 109/L. Total bilirubin £ 1.5 x upper limit of normal (ULN). ALT and AST < 2.5 x ULN in the absence of liver metastases, or < 5 x ULN in case of liver metastases. Creatinine clearance ³ 60ml/min (calculated according to Cockcroft-gault formula).
  • Patients should be contraceptive during the period of the trial until 8 weeks after the last administration of icotinib.
  • Able to comply with the required protocol and follow-up procedures, and able to receive oral medications.

排除标准

  • Patient was received irradiation of brain. Patient with meningeal metastases were confirmed by MRI or cytology test of cerebrospinal fluid.
  • Patient is received the treatment of Phenytoin, carbamazepine, rifampicin, phenobarbital, or St. John's Wort.
  • Patient was received EGFR Tyrosine Kinase Inhibitor or EGFR monoclonal antibody.
  • Interstitial pneumonia.Pericardial effusion, pleural effusion is uncontrolled .
  • Any unstable systemic disease (including active infection, uncontrolled hypertension, unstable angina, congestive heart failure, myocardial infarction within the previous year, serious cardiac arrhythmia requiring medication, hepatic, renal, or metabolic disease).
  • Any significant ophthalmologic abnormality ,especially severe dry eye syndrome ,keratoconjunctivitis sicca,Sjogren syndrome,severe exposure keratitis or any other disorder likely to increase the risk of corneal epithelial lesions.
  • Lack of physical integrity of the upper gastrointestinal tract, or malabsorption syndrome, or inability to take oral medication, or have active peptic ulcer disease.
  • The symptoms of increased intracranial pressure are uncontrolled after dehydration and cortisone treatment

研究组 & 干预措施

Gefitinib and Pemetrexed/platinum

Experimental

Gefitinib 250mg is Taken Orally on day 1-28,combined Pemetrexed (D1)+cisplatin (D1-3) chemotherapy or Pemetrexed (D1)+nedaplatin (D1) chemotherapy, every 28 days

干预措施: Gefitinib and Pemetrexed/platinum (Drug)

Gefitinib mono-therapy

Active Comparator

Gefitinib 250mg is Taken Orally everyday

干预措施: Gefitinib mono-therapy (Drug)

结局指标

主要结局

iPFS(intracranial progression free survival

时间窗: 2 years

defined as time from randomization to intracranial progressive disease or death.

次要结局

  • ORR(2 years)
  • intracranial objective response rate (iORR)(2 years)
  • PFS(Progression Free Survival)(2 years)
  • OS(Overall Survival)(3 years)
  • adverse events(3 years)

研究者

发起方
Sun Yat-sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Li-kun Chen

medical doctor

Sun Yat-sen University

研究点 (1)

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