Cannizzaro Maria Teresa, Inserra Maria Cristina, Passaniti Giulia, Celona Antonio, D'Angelo Tommaso, Romeo Placido, Basile Antonio
CAST Radiology Department, A.U.O. Policlinico "G.Rodolico-San Marco", Catania, Italy.
University of Catania, CAST Policlinico Hospital, Italy.
Heliyon. 2023 Apr 5;9(4):e15226. doi: 10.1016/j.heliyon.2023.e15226. eCollection 2023 Apr.
The development of cardiotoxicity induced by cancer treatments has emerged as a significant clinical problem, both in the short run, as it may influence drug administration in chemotherapeutic protocols, and in the long run, because it may determine adverse cardiovascular outcomes in survivors of various malignant diseases. Therefore, early detection of anticancer drug-related cardiotoxicity is an important clinical target to improve prevention of adverse effects and patient care. Today, echocardiography is the first-line cardiac imaging techniques used for identifying cardiotoxicity. Cardiac dysfunction, clinical and subclinical, is generally diagnosed by the reduction of left ventricular ejection fraction (LVEF) and global longitudinal strain (GLS). However, myocardial injury detected by echocardiography is preceded by other alterations, such as myocardial perfusion and mitochondrial and metabolic dysfunction, that can only be recognized by second-level imaging techniques, like cardiac magnetic resonance (CMR) and nuclear imaging, which, using targeted radiotracers, may help to provide information on the specific mechanisms of cardiotoxicity. In this review, we focus on the current and emerging role of CMR, as a critical diagnostic tool of cardiotoxicity in the very early phase, due to its availability and because it allows the contemporary detection of functional alterations, tissue alterations (mainly performed using T1, T2 mapping with the evaluation of extracellular volume-ECV) and perfusional alteration (evaluated with rest-stress perfusion) and, in the next future, even metabolic changes. Moreover, in the subsequent future, the use of Artificial Intelligence and big data on imaging parameters (CT, CMR) and oncoming molecular imaging datasets, including differences for gender and countries, may help predict cardiovascular toxicity at its earliest stages, avoiding its progression, with precise tailoring of patients' diagnostic and therapeutic pathways.
癌症治疗引起的心脏毒性的发展已成为一个重大的临床问题,短期内,它可能影响化疗方案中的药物给药;从长远来看,因为它可能决定各种恶性疾病幸存者的不良心血管结局。因此,早期检测抗癌药物相关的心脏毒性是改善不良反应预防和患者护理的重要临床目标。如今,超声心动图是用于识别心脏毒性的一线心脏成像技术。心脏功能障碍,无论是临床的还是亚临床的,通常通过左心室射血分数(LVEF)和整体纵向应变(GLS)的降低来诊断。然而,超声心动图检测到的心肌损伤之前会有其他改变,如心肌灌注、线粒体和代谢功能障碍,这些只能通过二级成像技术识别,如心脏磁共振(CMR)和核成像,它们使用靶向放射性示踪剂,可能有助于提供有关心脏毒性具体机制的信息。在本综述中,我们重点关注CMR作为心脏毒性早期关键诊断工具的当前和新兴作用,这是由于其可用性,并且它能够同时检测功能改变、组织改变(主要使用T1、T2映射并评估细胞外容积-ECV)和灌注改变(通过静息-负荷灌注评估),并且在未来,甚至还能检测代谢变化。此外,在后续的未来,利用人工智能以及关于成像参数(CT、CMR)和即将到来的分子成像数据集的大数据,包括性别和国家差异,可能有助于在心血管毒性最早阶段进行预测,避免其进展,从而精确制定患者的诊断和治疗路径。