Ades Felipe, Zardavas Dimitrios, Pinto Ana Catarina, Criscitiello Carmen, Aftimos Philippe, de Azambuja Evandro
Department of Medical Oncology, Jules Bordet Institute, Université Libre de Bruxelles, Brussels, Belgium.
Division of Early Drug Development for Innovative Therapies, Istituto Europeo di Oncologia, Via Ripamonti 435, 20133 Milano, Italy.
Breast. 2014 Aug;23(4):317-28. doi: 10.1016/j.breast.2014.04.002. Epub 2014 May 1.
Several breast cancer therapies can lead to cardiovascular toxicity: drugs such anthracyclines can cause permanent damage, anti-HER2 agents may cause transitory and reversible cardiac dysfunction and others, such as those used in endocrine therapy, primarily disturb lipid metabolism. Considering the seriousness of these complications, trials are now being conducted to address cardiotoxicity associated with new drugs; however, to fully understand their toxicity profiles, longer follow-up is needed. In this review, we compile the information available about cardiac toxicity related to well-established systemic breast cancer treatments, as well as newer drugs, including antiangiogenics, mTOR inhibitors and novel anti-HER2 agents. We also describe current and next generation cardiac biomarkers and functional tests that can optimize treatment and reduce and prevent the incidence of treatment-related cardiotoxicity.
如蒽环类药物可造成永久性损伤,抗HER2药物可能引起短暂且可逆的心脏功能障碍,而其他药物,如内分泌治疗中使用的药物,主要干扰脂质代谢。鉴于这些并发症的严重性,目前正在进行试验以解决与新药相关的心脏毒性问题;然而,为了全面了解它们的毒性特征,还需要更长时间的随访。在本综述中,我们汇总了有关与成熟的全身性乳腺癌治疗以及新药(包括抗血管生成药物、mTOR抑制剂和新型抗HER2药物)相关的心脏毒性的现有信息。我们还描述了当前和下一代心脏生物标志物以及功能测试,这些可以优化治疗并降低和预防治疗相关心脏毒性的发生率。