EUCTR2006-001707-11-NL进行中(未招募)不适用
Prospective, randomized, pharmacological intervention study; evaluating the effect of the angiotensin II-receptor (AT1) blocker candesartan versus placebo in prevention of trastuzumab-associated cardiotoxicity in patients with primary breast cancer treated with trastuzumab - M06HER
KI-Av0 个研究点开始时间: 2007年10月26日最近更新:
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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
- •Women aged =18 years
- •2.WHO: 0-2
- •3.Strongly HER2-positive breast cancer, defined as an immunohistochemistry score of 3+ using the HercepTestTM or gene amplification by fluorescence in situ hybridization, or chromogenic in situ hybridization (CISH)
- •4.Serum creatinine <140 umol/l or creatinine clearance > 50 ml/min (by Cockcroft-Gault formula)
- •5.Thyroid stimulating hormone between 0.5-3.9 MU/l
- •6.Blood pressure systolic = 140 mmHg diastolic = 90 mmHg is acceptable at randomization. However prior to the first administration of trastuzumab blood pressure should be regulated and should be systolic = 100 mmHg and = 180 mmHg and diastolic = 60 mmHg and = 100 mmHg (blood pressure should be regulated according to the guidelines of appendix 5).
- •7.LVEF ? 50% assessed by multigated angiography (MUGA) or cardiac ultrasound.
- •8.(Neo-) adjuvant regimen: trastuzumab start = 3 weeks after day 1 of the last anthracycline chemotherapy cycle
- •9.Trastuzumab treatment according standard medical care
- •10.Written informed consent to participate in the study
- •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
- •1.Prior anthracycline chemotherapy regimen or anti-HER2 therapy, or other prior biologic or immunotherapy for breast cancer treatment or any malignancy
- •2.Previous malignancy requiring chemotherapy or radiotherapy
- •3.Uncontrolled serious concurrent illness
- •4.Patients with New York Heart Association (NYHA) class III/IV congestive heart failure
- •5.Myocardial infarction < 6 months before randomization
- •6.Treatment with ACE inhibitors, ATII blockers, or lithium. Patients treated with ACE inhibitors or ATII blockers can switch (after randomization and during the chemotherapy period) to alternative antihypertensive therapy; see appendix 5.
- •7.History of hypersensitivity to the study medication
- •8.Pregnancy or breast feeding
研究者
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