Podlesnikar Tomaž, Berlot Boštjan, Dolenc Jure, Goričar Katja, Marinko Tanja
Department of Cardiology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Department of Cardiac Surgery, University Medical Centre Maribor, Maribor, Slovenia.
Front Cardiovasc Med. 2022 Jul 28;9:887705. doi: 10.3389/fcvm.2022.887705. eCollection 2022.
Radiotherapy (RT) is one of the pillars of cancer therapy. High-dose radiation exposure on the thorax is mainly used in the context of adjuvant RT after breast surgery, in lung and esophageal cancer, and as a complement to systemic treatment in lymphoma. Due to the anatomical proximity, the heart inevitably receives some radiation that can result in acute and chronic cardiotoxicity, leading to heart failure, coronary artery disease, pericardial and valvular heart disease. Current evidence suggests there is no safe radiation dose to the heart, which poses a need for early recognition of RT-induced cardiac injury to initiate cardioprotective treatment and prevent further damage. Multimodality cardiac imaging provides a powerful tool to screen for structural and functional abnormalities secondary to RT. Left ventricular ejection fraction, preferably with three-dimensional echocardiography or cardiovascular magnetic resonance (CMR), and global longitudinal strain with speckle-tracking echocardiography are currently the key parameters to detect cardiotoxicity. However, several novel imaging parameters are tested in the ongoing clinical trials. CMR parametric imaging holds much promise as T1, T2 mapping and extracellular volume quantification allow us to monitor edema, inflammation and fibrosis, which are fundamental processes in RT-induced cardiotoxicity. Moreover, the association between serum biomarkers, genetic polymorphisms and the risk of developing cardiovascular disease after chest RT has been demonstrated, providing a platform for an integrative screening approach for cardiotoxicity. The present review summarizes contemporary evidence of RT-induced cardiac injury obtained from multimodality imaging-echocardiography, cardiovascular computed tomography, CMR and nuclear cardiology. Moreover, it identifies gaps in our current knowledge and highlights future perspectives to screen for RT-induced cardiotoxicity.
放射治疗(RT)是癌症治疗的支柱之一。胸部高剂量辐射暴露主要用于乳腺癌手术后的辅助放疗、肺癌和食管癌治疗,以及作为淋巴瘤全身治疗的补充。由于解剖位置相邻,心脏不可避免地会受到一些辐射,这可能导致急性和慢性心脏毒性,进而引发心力衰竭、冠状动脉疾病、心包和瓣膜性心脏病。目前的证据表明,不存在对心脏安全的辐射剂量,这就需要早期识别放疗引起的心脏损伤,以便启动心脏保护治疗并防止进一步损害。多模态心脏成像为筛查放疗继发的结构和功能异常提供了有力工具。目前,左心室射血分数(最好采用三维超声心动图或心血管磁共振成像(CMR)测量)以及斑点追踪超声心动图测量的整体纵向应变是检测心脏毒性的关键参数。然而,一些新的成像参数正在正在进行的临床试验中进行测试。CMR参数成像很有前景,因为T1、T2映射和细胞外容积定量可让我们监测水肿、炎症和纤维化,这些是放疗引起心脏毒性的基本过程。此外,血清生物标志物、基因多态性与胸部放疗后发生心血管疾病风险之间的关联已得到证实,这为心脏毒性的综合筛查方法提供了一个平台。本综述总结了从多模态成像(超声心动图、心血管计算机断层扫描、CMR和核心脏病学)获得的关于放疗引起心脏损伤的当代证据。此外,它还指出了我们目前知识中的空白,并强调了筛查放疗引起心脏毒性的未来前景。