首页> 外文OA文献 >EACVI/HFA Cardiac Oncology Toxicity Registry in breast cancer patients: rationale, study design, and methodology (EACVI/HFA COT Registry)-EURObservational Research Program of the European Society of Cardiology.
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EACVI/HFA Cardiac Oncology Toxicity Registry in breast cancer patients: rationale, study design, and methodology (EACVI/HFA COT Registry)-EURObservational Research Program of the European Society of Cardiology.

机译:乳腺癌患者的EACVI / HFA心脏肿瘤毒性注册表:原理,研究设计和方法(EACVI / HFA COT注册表)-欧洲心脏病学会EUR观测研究计划。

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摘要

The goal of adjuvant anti-cancer therapies is cure with limited or no side effects, in particular long-term side effects with negative impact on quality of life. In the palliative setting disease control, quality of life and overall survival are important end points. Partly due to improvements in treatment, the population of cancer survivors is large and growing. However, anti-cancer drug-related cardiotoxicity (ADRC) is the leading cause of treatment-associated mortality in cancer survivors. It is one of the most common post-treatment problems among 5- to 10-year survivors of adult cancer. This is particularly true for breast cancer, the most common cancer in women. The EACVI/HFA COT registry is designed for comprehensive data collection and evaluation of the current European practice in terms of diagnosis and management of ADRC in breast cancer patients. The COT registry will be carried out in two continuing phases, the pilot study phase involving 13 countries followed by the long-term registry in which all the 56 ESC countries will be invited to participate. With the COT registry, several critical information will be obtained: on predisposing factors for the development of ADRC, the rate of subclinical LV dysfunction and its transition to overt heart failure, the clinical impact and outcome of ADRC.
机译:辅助抗癌治疗的目标是治愈,且副作用有限或没有副作用,尤其是长期副作用,会对生活质量造成负面影响。在姑息性疾病控制中,生活质量和整体生存是重要的终点。部分由于治疗的改善,癌症幸存者的人数庞大且正在增长。但是,抗癌药物相关的心脏毒性(ADRC)是癌症幸存者中与治疗相关的死亡率的主要原因。它是成年癌症5至10岁幸存者中最常见的治疗后问题之一。对于女性中最常见的癌症-乳腺癌尤其如此。 EACVI / HFA COT注册中心旨在针对乳腺癌患者中ADRC的诊断和管理全面收集和评估当前欧洲实践的数据。 COT注册将在两个连续的阶段中进行,先期研究阶段涉及13个国家,随后是长期注册,将邀请所有56个ESC国家参加。通过COT注册中心,将获得一些关键信息:关于ADRC发展的诱因,亚临床LV功能障碍的发生率及其向明显心力衰竭的过渡,ADRC的临床影响和结果。

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