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Cardiotoxicity due to targeted anticancer agents: a growing challenge

机译:由于靶向抗癌代理引起的心脏毒性:越来越大的挑战

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The emergence of various targeted anticancer agents has led us to uncharted territory secondary to their cardiotoxic potential with many burning questions, which in turn has led to the evolution of the cardio-oncology field. These targeted agents differ in their cardiovascular complication (CVC) potential even within the same class and it is very difficult to design screening tests that can predict CVCs. Moreover, there is a need for more research to answer many crucial questions, since these toxicities are unanticipated and can lead to poor overall survival of cancer patients. We still do not clearly understand the mechanism for such toxicity, risk factors, and natural history. A better understanding of the underlying risk factors and identification of biomarkers would help us develop protocols for appropriate monitoring strategies which in turn would help capture these toxicities at early stages. In this succinct review, we try to focus on CVC definition, summarize some published research, and point to areas of unmet need in this new field.
机译:各种靶向抗癌代理的出现使我们引起了次要的恐怖潜力的未知领域,其中许多燃烧的问题,这反过来导致了心动肿瘤学领域的演变。即使在同一类内,这些靶向剂的潜在含量差异(CVC)潜力也很差异,并且设计可以预测CVC的筛选测试是非常困难的。此外,需要更多的研究来回答许多关键问题,因为这些毒性被意识到并且可以导致癌症患者的整体存活差。我们仍然没有明确了解这种毒性,危险因素和自然历史的机制。更好地了解潜在的危险因素和生物标志物的识别将有助于我们制定适当的监测策略的协议,这反过来又会有助于捕获早期阶段的这些毒性。在这个简洁的评论中,我们尝试专注于CVC定义,总结一些已发表的研究,并指出了在这一新领域的未满足地区。

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