Geisberg Carrie, Pentassuglia Laura, Sawyer Douglas B
Division of Cardiovascular Medicine, Department of Medicine, Vanderbilt University Medical Center, 2220 Pierce Avenue, Room #383, Preston Research Building, Nashville, TN 37232, USA.
Curr Heart Fail Rep. 2012 Sep;9(3):211-8. doi: 10.1007/s11897-012-0098-4.
Damage to heart cells leading to heart failure is a known complication of well-established cancer therapies including anthracycline antibiotics and radiation therapy, and the cardiovascular complications of these therapies has been controlled in large part through dose limitations and modifications of delivery methods. Recent research into the cellular and molecular mechanisms for the cardiovascular effects of these therapies may lead to other cardioprotective strategies that improve effectiveness of cancer treatments. Newer cancer therapies that have been developed based upon specifically targeting oncogene signaling also have been associated with heart failure. Rapid development of a detailed understanding of how these agents cause cardiac dysfunction promises to improve outcomes in cancer patients, as well as stimulate concepts of cardiovascular homeostasis that will likely accelerate development of cardiovascular therapies.
导致心力衰竭的心脏细胞损伤是包括蒽环类抗生素和放射治疗在内的成熟癌症疗法的已知并发症,这些疗法的心血管并发症在很大程度上已通过剂量限制和给药方式的改变得到控制。最近对这些疗法心血管效应的细胞和分子机制的研究可能会带来其他心脏保护策略,从而提高癌症治疗的效果。基于特异性靶向癌基因信号传导而开发的新型癌症疗法也与心力衰竭有关。迅速深入了解这些药物如何导致心脏功能障碍,有望改善癌症患者的治疗结果,并激发心血管稳态的概念,这可能会加速心血管治疗的发展。