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临床试验/NCT00388089
NCT00388089已完成1 期

Phase I Study of Weekly Bortezomib (VELCADE, PS-341) and Weekly Topotecan (HYCAMTIN) in Solid Tumor Patients With an Emphasis on Small Cell Lung Cancer (SCLC)

University of California, Davis2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2004年12月最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
24
试验地点
2
主要终点
Safety

研究概览

简要总结

RATIONALE: Bortezomib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as topotecan, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving bortezomib together with topotecan may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of bortezomib and topotecan in treating patients with advanced solid tumors.

详细描述

OBJECTIVES:

Primary

  • Evaluate the safety and feasibility of bortezomib and topotecan hydrochloride in patients with advanced solid tumors.

Secondary

  • Determine the maximum tolerated dose (MTD) of bortezomib and topotecan hydrochloride in these patients.
  • Determine, preliminarily, the efficacy of this regimen in these patients.
  • Perform laboratory correlative studies on tumor tissue and blood samples from these patients to investigate potential predictors of response.
  • Obtain fresh tumor tissue for correlative studies from a subset of patients with small cell lung cancer treated at the MTD.

研究设计

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

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

Safety

时间窗: Monitored on an ongoing basis during the study

If cumulative toxicities are seen in subsequent treatment cycles, a decision regarding modification or discontinuation of the study drug and/or patient enrollment will be made by the sponsor in conjunction with the investigator.

次要结局

  • Toxicity(On Day 8 and at beginning of subsequent cycles)
  • Response rate(At baseline and every 2 courses during treatment)
  • Best response(From start of treatment until disease progression/recurrence)
  • Survival(From registration to time of death due to any cause)
  • Progression-free survival(From registration to the first observation of disease progression or death due to any cause)
  • Topoisomerase levels as assessed by western blot and tumor tissue biopsy(From pre-treatment to post-treatment)
  • NF-kB and BCL-2 family activity as assessed by immunohistochemistry(From pre-treatment to post-treatment)
  • Loss of p27 as assessed by immunohistochemistry(From pre-treatment to post-treatment)
  • Hypoxia-induced plasma proteins as measured by enzyme-linked immunosorbent assay (ELISA)(From pre-treatment to post-treatment)
  • Shed tumor DNA in plasma(From pre-treatment to post-treatment)
  • Biological activity of bortezomib as measured by flow cytometry(From pre-treatment to post-treatment)

研究者

申办方类型
Other

研究点 (2)

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