CTRI/2018/05/013694尚未招募4 期
A randomized trial to compare gefitinib plus chemotherapy vs chemotherapy alone in EGFR positive and T790M mutation negative advanced Non-small cell lung cancer patients after progression on first line gefitinib.
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Patients of either sex aged 18 years or older
- •2.Histologically or cytologically proven diagnosis of NSCLC other than predominantly squamous cell histology with an activating EGFR tyrosine kinase (TK) mutation
- •3.Performance Status 0-1
- •4.Progressive disease on first-line TKI
- •5.T790M mutation negative status.
- •6.Written informed consent prior to study treatment.
- •7.All patients should have achieved either a stable disease or objective response to the first line TKI and later develop disease progression.
- •8.Patients with Brain metastasis
排除标准
- •1.Prior chemotherapy or other systemic anti-cancer treatment (excluding Gefitinib).
- •2.Past medical history of interstitial lung disease, drug-induced interstitial disease, radiation pneumonitis which required steroid treatment or any evidence of clinically active interstitial lung disease.
- •3.Neutrophils <1.5 x 109/L or platelets <100 x 109/L.
- •4.Serum bilirubin >1.5 x the upper limit of normal (ULN).
- •5.Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >3 x ULN in the absence of liver metastases, or >5 x ULN in the presence of liver metastases.
- •6.Creatinine clearance <45 mL/min calculated by either Cockcroftâ??Gault or other validated methods.
- •7.Any evidence of severe or uncontrolled systemic disease (e.g. unstable or uncompensated respiratory, cardiac, renal or hepatic disease) as judged by the investigator.
- •8.Other co-existing malignancies or malignancies diagnosed within the last 5 years (except non-melanoma skin cancer or in-situ cervical cancer).
- •9.Life expectancy of less than 3 months
- •10.Pregnant females
研究者
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