Therapy-induced cardiotoxicity in breast cancer patients: a well-known yet unresolved problem.

Diana Ruxandra Florescu, Diana Elena Nistor
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Abstract

Breast cancer is the second most commonly diagnosed cancer, being one of the main health issues that needs to be addressed worldwide. New therapies have led to a remarkable increase in survival rates, which is unfortunately overshadowed by their negative impact on cardiac structure and function in disease-free patients. Since anthracyclines and trastuzumab cause the most undesired outcome in breast cancer patients - cardiac-related mortality, they have been widely studied. However, other therapies (such as hormonal therapy, tyrosine kinase inhibitors, anti-VEGF drugs etc.) can also affect the cardiovascular system and lead to ischemia, hypertension or vascular thromboembolism. Even though excessive research has been conducted in thepast decades, there are still no guidelines regarding the most adequate methods neither to detect and prevent severe cardiotoxicity that can finally lead to heart failure and ultimately death nor for the further management of patients after cardiotoxicity is detected. Biomarkers of ischemia (troponins T and I) and of overload (BNP and NT-proBNP) in association with periodic echocardiographies (assessment of the global longitudinal strain) are two of the most important means used by physicians in the evaluation of cardiac disease in this group of patients. Given that no internationally accepted guidelines for screening and surveillance of different populations exist, the cardio-oncology team is crucial in the management of these patients, their collaboration resulting in individualized treatment regimens. After careful evaluation of different variables (treatment effects, malignancy status, and the patient's pre-existing conditions), a decision is made to either reduce the dosage or rate of administration, change the medication or interrupt the treatment and initiate the cardioprotective therapeutic associations. Consequently, it is an absolute necessity the development of customized treatment guidelines and the conduction of multiple clinical studies in order to demonstrate their effect on long-term survival.

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乳腺癌患者治疗引起的心脏毒性:一个众所周知但尚未解决的问题。
乳腺癌是第二大最常诊断出的癌症,也是全世界需要解决的主要健康问题之一。新疗法使患者的存活率显著提高,但不幸的是,这些疗法对无病症患者的心脏结构和功能造成的负面影响却掩盖了这一成果。由于蒽环类和曲妥珠单抗会导致乳腺癌患者最不希望出现的结果--与心脏相关的死亡,因此它们被广泛研究。然而,其他疗法(如激素疗法、酪氨酸激酶抑制剂、抗血管内皮生长因子药物等)也会影响心血管系统,导致缺血、高血压或血管血栓栓塞。尽管在过去几十年中进行了大量研究,但仍然没有关于最适当的方法的指导方针,既不能检测和预防严重的心脏毒性,这种毒性最终会导致心力衰竭和死亡,也不能在检测到心脏毒性后对患者进行进一步管理。缺血生物标志物(肌钙蛋白 T 和 I)和负荷过重生物标志物(BNP 和 NT-proBNP)与定期超声心动图检查(评估总体纵向应变)是医生用于评估这类患者心脏疾病的两种最重要的方法。鉴于目前还没有国际公认的针对不同人群的筛查和监测指南,心脏肿瘤团队在这些患者的管理中起着至关重要的作用,通过他们的合作可以制定出个性化的治疗方案。在对不同的变量(治疗效果、恶性肿瘤状态和患者的原有疾病)进行仔细评估后,决定减少用药剂量或用药速度、更换药物或中断治疗并启动心脏保护治疗联合疗法。因此,绝对有必要制定个性化的治疗指南,并开展多项临床研究,以证明其对长期生存的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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