此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Phase II Study to Evaluate Tariquidar (XR9576), a Selective MDR-1 Inhibitor, in Chemotherapy Resistant Advanced Breast Cancer

2012年5月22日 更新者:QLT Inc.

The primary objective of this phase II study is to assess if XR9576, a selective MDR-1 inhibitor, is able to reverse primary doxorubicin or taxane resistance in advanced breast cancer. Clinical activity will be measured by objective tumor response rates observed after treatment with XR9576 in combination with taxane or anthracycline containing chemotherapy in patients previously resistant to the same agent(s).

The secondary objectives of the study are to assess the biological activity of XR9576 and evaluate MDR-1 expression in these tumors. The MDR-1 inhibitory activity of XR9576 will be evaluated by serial sestamibi scans of the tumor. MDR-1 expression will be detected by immunohistochemistry.

研究概览

地位

完全的

条件

干预/治疗

研究类型

介入性

注册

30

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Florida
      • Jacksonville、Florida、美国、32207-5905
        • Florida Oncology Associates
    • Indiana
      • Vincennes、Indiana、美国、47591
        • Medical Center of Vincennes
    • Texas
      • Arlington、Texas、美国、76012
        • Arlington Cancer Center
      • Houston、Texas、美国、77030-4009
        • MD Anderson Cancer Center

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人
  • 年长者

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion criteria:

  • Histologically proven breast cancer with primary resistance to anthracyclines (doxorubicin, epirubicin) or taxane (paclitaxel, docetaxel) or both. Primary chemotherapy resistance is defined for the purpose of this protocol as any of the following:

    1. Progression after a minimum of 1 cycles of therapy, or
    2. Stable disease after a minimum of 2 cycles of therapy or,
    3. Relapse within 6 months after completion of an anthracycline or/and taxane containing chemotherapy regimen.
  • Patients with anthracycline/taxane resistance INOPERABLE, locally advanced breast cancer are eligible.
  • Patients must have measurable disease as defined by the RECIST criteria in their breast/nodal regions or at a distant organ site(s).
  • There is no limit on prior hormonal therapies but only one prior chemotherapy for metastatic breast cancer is allowed.
  • Patients may receive concomitant bisphosphonate therapy for bone metastasis.
  • Patients may continue Herceptin if it has previously been started. Herceptin cannot be added to the chemotherapy regimen as a new agent at the same time when XR9576 is initiated.
  • Patients much have recovered from acute toxic effects of any prior therapy.
  • Zubrod performance status less than or equal to 2.
  • Adequate bone marrow function: platelets greater than or equal to 100,000/mm3, ANC greater than or equal to 1500 cells/mm3, hemoglobin greater than or equal to 8g/dl.
  • Normal renal function: creatinine less than or equal to 2.0 mg/dl. Adequate liver function: bilirubin less than or equal to 1.5 mg/dl. Transaminase (SGOT) and alkaline phosphatase must be less than or equal to 1.5 x of the upper limit of normal in the absence of bone or liver metastasis, or less than or equal to 2.5 x of the upper limit of normal in the presence of radiologically apparent liver metastasis or bone metastasis, respectively.
  • Female patients must be of non-lactating and using adequate contraception if premenopausal. Beta-HCG will be checked in premenopausal patients if clinically indicated.
  • Patients with brain metastases whose disease remained stable for more than 3 months after completing therapy to the brain are eligible.
  • Written informed consent.

Exclusion criteria:

  • More than 1 chemotherapy regimen for metastatic breast cancer.
  • Patients who relapsed more than 6 months after completion of anthracycline or taxane therapy.
  • Current treatment with a non-taxane, non-anthracycline based chemotherapy.
  • Uncontrolled psychiatric, or social (addictive) disorders that would preclude obtaining informed consent or patient participation in the study.
  • Clinical contraindication of continued anthracycline or taxane therapy. For patients who show primary resistance to anthracyclines this includes greater than 300 mg/m2 maximum life-time cumulative dose of doxorubicin, symptomatic heart failure, history of heart failure, recent myocardial infarction (less than 6 months) or left ventricular ejection fraction below normal range. For patients with primary resistance to taxanes, persistent grade 2 or greater neuropathy (neuropathy that interferes with function).
  • Patients with operable primary breast cancer are not eligible.
  • Patients who have developed primary resistance to the chemotherapy combination of doxorubicin/docetaxel.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:非随机化
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Tariquidar

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

调查人员

  • 研究主任:Graeme R Boniface、Sponsor GmbH

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2001年11月1日

初级完成 (实际的)

2003年6月1日

研究完成 (实际的)

2003年6月1日

研究注册日期

首次提交

2002年11月4日

首先提交符合 QC 标准的

2002年11月5日

首次发布 (估计)

2002年11月6日

研究记录更新

最后更新发布 (估计)

2012年5月23日

上次提交的符合 QC 标准的更新

2012年5月22日

最后验证

2012年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • TQD BRST 001

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅