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临床试验/NCT00482755
NCT00482755已完成2 期

A Feasibility Study of Pre-Operative Sunitinib (SU11248) With Multiple Pharmacodynamic Endpoints in Patients With T1c-T3 Operable Carcinoma of the Breast

NCIC Clinical Trials Group4 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2009年4月8日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
4
试验地点
4
主要终点
Feasibility

研究概览

简要总结

RATIONALE: Sunitinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Giving sunitinib before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

PURPOSE: This phase II trial is studying how well sunitinib works in treating patients with newly diagnosed stage II or stage IIIA breast cancer that can be removed by surgery.

详细描述

OBJECTIVES:

Primary

  • Determine the feasibility of neoadjuvant sunitinib malate in patients with newly diagnosed, resectable stage II-IIIA breast cancer.

Secondary

  • Determine the nature, severity, and frequency of adverse events in patients treated with this drug.
  • Determine the response rate in patients treated with this drug.
  • Evaluate markers of angiogenesis (e.g., VEGF receptor, platelet-derived growth factor receptor, circulating plasma VEGF, sVEGFR-2, sVEGFR-3, sKIT, and tumor vascularity) both pre- and post-treatment.
  • Examine the role of both host- and tumor-specific genes pertaining to response and toxicity.
  • Compare tumor vascular parameters pre- and post-treatment using DCE-MRI.
  • Compare cell death and tumor microcirculation pre- and post-treatment using contrast-enhanced spectroscopic and microbubble contrast-enhanced ultrasound.
  • Compare tumor metabolic activity pre- and post-treatment using fludeoxyglucose F 18-PET.

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
18 Years 至 120 Years(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

Feasibility

次要结局

  • Nature, severity, and frequency of adverse events
  • Activity (response rate)
  • Markers of angiogenesis pre- and post-treatment
  • Role of both host- and tumor-specific genes pertaining to response and toxicity
  • Comparison of tumor vascular parameters pre- and post-treatment
  • Comparison of cell death and tumor microcirculation pre- and post-treatment
  • Comparison of tumor metabolic activity pre- and post-treatment

研究者

申办方类型
Network
责任方
Sponsor

研究点 (4)

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