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临床试验/EUCTR2007-003634-42-DE
EUCTR2007-003634-42-DE进行中(未招募)不适用

Prospective phase II trial using Capecitabine and Trastuzumab for therapy of female patients with cerebral metastasizing, HER2-overexpressing breast cancer - HERXE

Klinikum der Universität München, Standort Großhadern0 个研究点开始时间: 2007年8月21日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • - Histological proven metastasizing breast cancer in women
  • - HER2-new-overexpression (IHC3+ or IHC2+/FISH+)
  • - Documented CNS metastases and/or Meningeosis carcinomatosa which are (neurosurgical) inoperable
  • - if no irradiation has been performed before study treatment (chemoimmunotherapy) it will be conducted in
  • - If a previous irridiation took place and it is not clinically indicated to be continued, this chemoimmunotherapy will be conducted analog and squentiell to study treatment after previous irradiation
  • - Besides Capecitabine all prior adjuvant /neoadjuvant chemotherapies possible
  • - Patients have to be treated with taxanes and Trastuzumab (not necessarily in combination) before, excluding cases of primary inoperable CNS metastases
  • - Prior hormone therapy is allowed
  • - Age between 18 and 75 years
  • - Performance status (Karnofsky) >= 70%
  • - Life expectancy >= 16 weeks
  • - Signed informed consent after complete information by the investigator before study specific treatment.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Pregnant or breast-feeding women (women with child-bearing potential must use effective contraception)
  • - Missing informed consent
  • - Prior treatment with Capecitabine
  • - opportunity of neurosurgery
  • - Patients, who took part in a clinical trial within 30 days prior to study entry
  • - Psychological, familiar, sociological or geographic circumstances that prevent follow-up medical treatment or treatment according to protocoll
  • - patients with following cardiovascular diseases/risk factors are excluded:
  • - previous congestive heartfailure
  • - high risk of uncontrolled arrhythmia
  • - angina pectoris which needs medical treatment
  • - clinical significant valvular insufficiency
  • - signs of transmural infarction in ECG
  • - not adjustable hypertension

研究者

发起方
Klinikum der Universität München, Standort Großhadern

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