跳至主要内容
临床试验/NCT00127049
NCT00127049Unknown2 期

A Prospective Multicenter Phase II Trial of Gemcitabine, Cisplatin, and Ifosfamide (GIP) in Patients With Relapsed Non-Seminomatous Germ-Cell Tumors (NSGCT) and a Predicted Favorable Prognosis

Gustave Roussy, Cancer Campus, Grand Paris1 个研究点 分布在 1 个国家目标入组 37 人开始时间: 2004年12月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
入组人数
37
试验地点
1
主要终点
Complete response rate

研究概览

简要总结

This is a prospective multicenter phase II trial of gemcitabine, cisplatin, and ifosfamide (GIP) in patients with relapsed non-seminomatous germ-cell tumors (NSGCT) and a predicted favorable prognosis.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
16 Years 至 —(Child, Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •Patients older than 16 years
  • •Histologically-proven disseminated (non stage I) NSGCT, or diagnosis of NSGCT based on very elevated serum human chorionic gonadotropin (HCG) and/or alpha fetoprotein (AFP)
  • •Relapsed disease classified as good prognosis according to the Memorial Sloan-Kettering Cancer Center (MSKCC) classification criteria:
  • •Testicular primary site
  • •Prior treatment limited to one program (or 6 or fewer cycles of cisplatin)
  • •Either a complete response or a partial response with normal serum AFP and HCG
  • •Relapse documented by rising AFP and/or HCG or by a biopsy
  • •No previous carcinoma, except basal-cell carcinoma of the skin
  • •Adequate renal function: measured or calculated creatinine clearance> 60 ml/min
  • •Absolute granulocyte count >= 1,500/mm3, platelets >= 100,000 mm3, bilirubin < 1.5 fold the upper normal value
  • •Signed informed consent.

排除标准

  • •Patients infected by the human immunodeficiency virus (HIV)
  • •Patients who do not fit inclusion criteria

结局指标

主要结局

Complete response rate

次要结局

  • Toxicity
  • Progression free survival
  • Overall survival

研究者

申办方类型
Other

研究点 (1)

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