Cardiac magnetic resonance imaging consistently identified early declines in left ventricular ejection fraction and subclinical dysfunction before changes were detectable on echocardiography.
Systematic Review
Does cardiac magnetic resonance imaging detect early and late cardiotoxic changes in cancer patients treated with anthracyclines?
CMR is a sensitive noninvasive tool capable of detecting subclinical anthracycline-induced cardiotoxicity through early changes in strain, tissue mapping (T1, T2, ECV), and volumetric indices, often before overt LVEF declines.
Anthracyclines are a cornerstone of cancer therapy, yet they carry a significant risk of cardiotoxicity, which may present as subclinical myocardial injury or overt heart failure. Timely detection is essential to prevent irreversible cardiac dysfunction and safeguard long-term quality of life. Cardiac magnetic resonance (CMR) imaging—capable of quantifying myocardial structure, function, and tissue characteristics—has emerged as a leading modality in this context. This systematic review evaluates the role of CMR in detecting both early and late cardiotoxic changes after anthracycline exposure. We conducted a systematic search in accordance with PRISMA 2020 guidelines, searching PubMed, Embase, Scopus and Web of Science for studies involving CMR assessment in patients treated with anthracyclines. We extracted data on changes in functional parameters, volumetric indices, strain measurements, and tissue characterization before, during, and after anthracycline therapy in patients receiving active chemotherapy, and differences of these parameters compare to healthy adults or their pretreatment CMR scan in long term cancer survivors. Across the 26 eligible studies, CMR consistently identified early declines in left ventricular ejection fraction, often before changes were detectable on echocardiography. More sensitive markers, including increases in the left ventricular end-systolic volume and alterations in strain parameters, provided early signs of subclinical dysfunction. Tissue mapping techniques revealed significant increases in native T1, T2, and extracellular volume (ECV), correlating with diffuse myocardial injury, even in the absence of late gadolinium enhancement. In long-term survivors, persistent abnormalities in strain and ECV were observed, highlighting the enduring nature of anthracycline induced cardiotoxicity. Right ventricular and left atrial remodeling, while less frequently assessed, emerged as clinically relevant and prognostically significant. CMR is a promising noninvasive tool that enables early detection and monitoring of anthracycline-induced cardiotoxicity, aiding risk stratification and timely cardioprotective interventions in cancer patients.
Motevalli et al. (Wed,) conducted a systematic review in Anthracycline-induced cardiotoxicity. Cardiac magnetic resonance imaging (CMR) vs. Echocardiography or baseline/healthy controls was evaluated on Detection of early and late cardiotoxic changes. Cardiac magnetic resonance imaging consistently identified early declines in left ventricular ejection fraction and subclinical dysfunction before changes were detectable on echocardiography.