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临床试验/ACTRN12611000013965
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

发起方
Sydney Cancer Centre

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