跳至主要内容
临床试验/NCT00014274
NCT00014274已完成2 期

Randomized Phase II/III Study Assessing Gemcitabine/Carboplatin And Methotrexate/Carboplatin/Vinblastine In Previously Untreated Patients With Advanced Urothelial Cancer Ineligible For Cisplatin Based Chemotherapy

European Organisation for Research and Treatment of Cancer - EORTC58 个研究点 分布在 11 个国家目标入组 238 人开始时间: 2001年1月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
238
试验地点
58
主要终点
Duration of survival

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. It is not yet known which combination chemotherapy regimen is most effective for transitional cell cancer of the urothelium.

PURPOSE: Randomized phase II/III trial to compare different combination chemotherapy regimens in treating patients who have transitional cell cancer of the urothelium.

详细描述

OBJECTIVES:

  • Compare the antitumor activity of gemcitabine and carboplatin vs methotrexate, carboplatin, and vinblastine in patients with transitional cell cancer of the urothelium who are ineligible for cisplatin-based chemotherapy.
  • Compare the toxicity and acute and intermediate (1-2 years) side effects of these regimens in these patients.
  • Compare the complete response rates, progression-free survival, and overall survival of patients treated with these regimens.
  • Compare the symptoms and quality of life of patients treated with these regimens.

OUTLINE: This is a randomized, multicenter study. Patients are randomized to one of two treatment arms.

  • Arm I: Patients receive methotrexate* IV and vinblastine IV on days 1, 15, and 22 and carboplatin IV over 1 hour on day 1. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
  • Arm II: Patients receive gemcitabine IV over 30 minutes on days 1 and 8 and carboplatin IV over 1 hour on day 1. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

NOTE: * Methotrexate is omitted for patients with pleural effusion or ascites until complete resolution and for patients with a glomerular filtration rate less than 30 mL/min or creatinine greater than 2 mg/dL

研究设计

研究类型
Interventional
分配方式
Randomized
主要目的
Treatment

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Duration of survival

次要结局

  • Response as assessed by RECIST criteria
  • Toxicity as assessed by CTC v2

研究者

申办方类型
Network
责任方
Sponsor

研究点 (58)

Loading locations...

相似试验

Combination Chemotherapy in Treating Patients With... | 临床试验