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临床试验/NCT00107484
NCT00107484已完成2 期

Phase II Study of Combidex in Axillary Node Staging in Breast Cancer

Virginia Commonwealth University1 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2005年9月1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
3
试验地点
1
主要终点
Utility of magnetic resonance imaging using ferumoxtran-10 in identifying metastases to axillary lymph nodes

研究概览

简要总结

RATIONALE: Diagnostic procedures, such as magnetic resonance imaging (MRI) using ferumoxtran-10, may help find and diagnose breast cancer that may have spread to the axillary lymph nodes and may help in planning breast cancer treatment.

PURPOSE: This phase II trial is studying how well MRI using ferumoxtran-10 works in finding metastases to the axillary lymph nodes in patients with invasive breast cancer.

详细描述

OBJECTIVES:

Primary

  • Determine the utility of magnetic resonance (MR) imaging using ferumoxtran-10 in identifying metastases to the axillary lymph nodes in patients with invasive breast cancer.

Secondary

  • Determine the changes in MR T1 and T2 signal intensity in primary breast tumors after administration of this drug to these patients.
  • Determine the potential of delayed imaging, in terms of defining tumor boundaries, in these patients.

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
Diagnostic
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
否

入选标准

  • •DISEASE CHARACTERISTICS:
  • •Histologically or cytologically confirmed invasive breast cancer
  • •Candidate for sentinel lymph node biopsy and/or axillary lymph node dissection
  • •Hormone receptor status:
  • •Not specified
  • •PATIENT CHARACTERISTICS:
  • •18 and over
  • •Male or female
  • •Menopausal status
  • •Not specified
  • •Performance status
  • •Not specified
  • •Life expectancy
  • •Not specified
  • •Hematopoietic
  • •WBC ≥ 3,000/mm^3
  • •Absolute neutrophil count ≥ 1,500/mm^3
  • •Platelet count > 100,000/mm^3
  • •Ferritin ≤ 350 ng/mL*
  • •Transferrin saturation level ≤ 40%* NOTE: *Patients with lab values above these limits may be eligible provided there is no hemochromatosis by hematology consultation
  • •Bilirubin normal
  • •AST and ALT ≤ 2.5 times upper limit of normal
  • •Alkaline phosphatase normal
  • •PT normal
  • •Albumin normal
  • •No history of cirrhosis
  • •Creatinine normal OR
  • •Creatinine clearance > 60 mL/min
  • •Cardiovascular
  • •No symptomatic congestive heart failure
  • •No unstable angina pectoris
  • •No cardiac arrhythmia
  • •Not pregnant or nursing
  • •Negative pregnancy test
  • •Medically stable
  • •No ongoing or active infection
  • •No history of allergic reaction attributed to compounds of similar chemical or biological composition to ferumoxtran-10 (e.g., iron preparations, parenteral iron, parenteral dextran, parenteral iron-dextran, or parenteral iron-polysaccharide preparations)
  • •No history of allergic reaction to any contrast media
  • •No immunodeficiency that would predispose patient to a specific or non-specific mediator release
  • •No contraindication to MRI, including any of the following:
  • •Severe claustrophobia
  • •Pacemaker
  • •Aneurysm clips
  • •Defibrillators
  • •Certain types of replacement joints
  • •Other institutional contraindication to MRI
  • •No psychiatric illness or social situation that would preclude study compliance
  • •No other uncontrolled illness
  • •PRIOR CONCURRENT THERAPY:
  • •Biologic therapy
  • 另有 10 项未显示

排除标准

  • 未提供

结局指标

主要结局

Utility of magnetic resonance imaging using ferumoxtran-10 in identifying metastases to axillary lymph nodes

时间窗: 2 years

次要结局

  • Changes in MR T1 and T2 signal intensity(2 years)

研究者

申办方类型
Other

研究点 (1)

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