首页> 外文期刊>BMC Cancer >Rationale and design of the Multidisciplinary Approach to Novel Therapies in Cardiology Oncology Research Trial (MANTICORE 101 - Breast): a randomized, placebo-controlled trial to determine if conventional heart failure pharmacotherapy can prevent trastuzumab-mediated left ventricular remodeling among patients with HER2+ early breast cancer using cardiac MRI
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Rationale and design of the Multidisciplinary Approach to Novel Therapies in Cardiology Oncology Research Trial (MANTICORE 101 - Breast): a randomized, placebo-controlled trial to determine if conventional heart failure pharmacotherapy can prevent trastuzumab-mediated left ventricular remodeling among patients with HER2+ early breast cancer using cardiac MRI

机译:心脏病学肿瘤研究试验中新疗法的多学科方法的原理和设计(MANTICORE 101-乳房):一项随机安慰剂对照试验,用于确定常规心力衰竭药物治疗是否可以预防曲妥珠单抗介导的HER2 +早期乳腺癌患者的左心室重构心脏核磁共振检查

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Background MANTICORE 101 - Breast (Multidisciplinary Approach to Novel Therapies in Cardiology Oncology Research) is a randomized trial to determine if conventional heart failure pharmacotherapy (angiotensin converting enzyme inhibitor or beta-blocker) can prevent trastuzumab-mediated left ventricular remodeling, measured with cardiac MRI, among patients with HER2+ early breast cancer. Methods/Design One hundred and fifty-nine patients with histologically confirmed HER2+ breast cancer will be enrolled in a parallel 3-arm, randomized, placebo controlled, double-blind design. After baseline assessments, participants will be randomized in a 1:1:1 ratio to an angiotensin-converting enzyme inhibitor (perindopril), beta-blocker (bisoprolol), or placebo. Participants will receive drug or placebo for 1 year beginning 7 days before trastuzumab therapy. Dosages for all groups will be systematically up-titrated, as tolerated, at 1 week intervals for a total of 3 weeks. The primary objective of this randomized clinical trial is to determine if conventional heart failure pharmacotherapy can prevent trastuzumab-mediated left ventricular remodeling among patients with HER2+ early breast cancer, as measured by 12 month change in left ventricular end-diastolic volume using cardiac MRI. Secondary objectives include 1) determine the evolution of left ventricular remodeling on cardiac MRI in patients with HER2+ early breast cancer, 2) understand the mechanism of trastuzumab mediated cardiac toxicity by assessing for the presence of myocardial injury and apoptosis on serum biomarkers and cardiac MRI, and 3) correlate cardiac biomarkers of myocyte injury and extra-cellular matrix remodeling with left ventricular remodeling on cardiac MRI in patients with HER2+ early breast cancer. Discussion Cardiac toxicity as a result of cancer therapies is now recognized as a significant health problem of increasing prevalence. To our knowledge, MANTICORE will be the first randomized trial testing proven heart failure pharmacotherapy in the prevention of trastuzumab-mediated cardiotoxicity. We expect the findings of this trial to provide important evidence in the development of guidelines for preventive therapy. Trial Registration ClinicalTrials.gov: NCT01016886
机译:背景技术101-乳腺癌(心脏病学研究中新疗法的多学科方法)是一项随机试验,用于确定常规心力衰竭药物治疗(血管紧张素转化酶抑制剂或β受体阻滞剂)是否可以预防曲妥珠单抗介导的左心室重构,采用心脏MRI进行测量在患有HER2 +早期乳腺癌的患者中。方法/设计将对经组织学证实为HER2 +乳腺癌的159例患者进行3臂平行,随机,安慰剂对照,双盲设计。在进行基线评估后,参与者将以1:1:1的比例随机分配至血管紧张素转化酶抑制剂(培哚普利),β受体阻滞剂(比索洛尔)或安慰剂。在曲妥珠单抗治疗前7天开始,参与者将接受1年的药物或安慰剂治疗。所有组的剂量将按耐受性系统地调整剂量,间隔1周,共3周。这项随机临床试验的主要目的是确定常规心力衰竭药物治疗是否可以预防曲妥珠单抗介导的HER2 +早期乳腺癌患者的左心室重构,这是通过心脏MRI检查左心室舒张末期容积12个月的变化来衡量的。次要目标包括:1)在HER2 +早期乳腺癌患者的心脏MRI上确定左心室重构的演变,2)通过评估血清生物标志物和心脏MRI的心肌损伤和细胞凋亡的存在,了解曲妥珠单抗介导的心脏毒性的机制, 3)在HER2 +早期乳腺癌患者的心脏MRI上将心肌细胞损伤和细胞外基质重塑的心脏生物标志物与左心室重塑相关联。讨论癌症治疗引起的心脏毒性现已被认为是患病率上升的重要健康问题。据我们所知,MANTICORE将是第一个经证实的心力衰竭药物治疗预防曲妥珠单抗介导的心脏毒性的随机试验。我们希望该试验的结果为预防性治疗指南的制定提供重要证据。试验注册ClinicalTrials.gov:NCT01016886

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