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临床试验/NL-OMON35127
NL-OMON35127已完成2 期

A randomized phase II trial of docetaxel plus carboplatin versus docetaxel in hormone refractory prostate cancer patients who have progressed after response to prior docetaxel chemotherapy: RECARDO STUDY - RECARDO

Vrije Universiteit Medisch Centrum0 个研究点目标入组 150 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
入组人数
150

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

年龄范围
18 至 99(—)

入选标准

  • 1. 18 years and above.
  • 2. Histologically proven hormone refractory prostate adenocarcinoma.
  • 3. PSA and/or clinical response on prior docetaxel-based chemotherapy with a progression free interval of over 3 months.
  • 4. Last PSA value * 5 ng/ml within 2 weeks prior to registration (HYBRITECH equivalent)
  • 5. Patients without surgical castration must continue on LHRH agonist therapy
  • 6. ECOG performance status * 2
  • 7. Gleason score 8-10
  • 8. Adequate haematological, liver and renal function.

排除标准

  • 1. More than 1 line of chemotherapy.
  • 2. Prior platinum chemotherapy.
  • 3. Radiotherapy within 2 weeks prior to treatment start.
  • 4. Uncontrolled hypercalcemia.
  • 5. Evidence of symptomatic brain and leptomeningeal metastatic disease.
  • 6. Previous or concurrent malignancies at other sites (except basal squamous cell carcinoma of the skin).

研究者

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A randomized phase II trial of docetaxel plus... | 临床试验