ACTRN12611000013965招募中未知
Exploration of differences in tolerance between Caucasian and Asian non-small cell lung cancer patients receiving palliative chemotherapy with carboplatin and paclitaxel
Sydney Cancer Centre0 个研究点目标入组 120 人开始时间: 2011年1月6日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •Asian or Caucasian patients.
- •- Histologically confirmed advanced non-small cell lung cancer patients
- •- receiving chemotherapy with carboplatin AUC 6 and paclitaxel 175 mg/m2
- •- Age greater than or equal to 18.
- •- Eastern Cooperative Oncology Group (ECOG)Performance Status of 0-2.
- •- Ability to comply with the planned procedures and provide written evidence of informed consent.
- •- Adequate haematology and biochemistry. (Haemoglobin>100 g/L, White blood cell count >4.0 x 109/L, neutrophil count > 1.5 × 109, platelets >100 x 109/L; Aspartate transaminase (AST), Alanine transaminase (ALT) and bilirubin < 1.5 x ULN (AST, ALT < 5 x upper limit of normal in case liver metastases); calculated creatinine clearance according to Corkroft formula > 60 ml/min.
排除标准
- •- Patients who require dose adjustment.
- •- Clinical evidence of active brain metastases.
- •- Suspected or documented bone marrow involvement.
- •- Significant intercurrent illness including active infection, inflammatory bowel disease or other uncontrolled autoimmune disease.
- •- The requirement for ongoing systemic treatment with corticosteroids or other immunosuppressive therapy.
- •- Patients who have had chemotherapy 4 weeks prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier.
- •- Ongoing major side effects from radiology.
- •- Other active malignancy.
- •- Known allergy to any of the investigational agents.
研究者
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