Ibrahim El-Sayed H, Chaudhary Lubna, Cheng Yee-Chung, Sosa Antonio, An Dayeong, Charlson John
1Medical College of Wisconsin, Milwaukee, USA.
2Northwestern University, Evanston, USA.
Radiol Oncol. 2025 Feb 27;59(1):79-90. doi: 10.2478/raon-2025-0012. eCollection 2025 Mar 1.
Over the past few decades, many studies have focused on anthracyclines effect on the heart (cardiotoxicity), but only a few have focused on sarcoma. In this study, we harness the capabilities of advanced cardiac magnetic resonance imaging (MRI) for characterizing anthracyclines-induced cardiotoxicity in sarcoma and compare the results to those from breast cancer patients.
The patients receive an MRI exam at three timepoints: baseline (pre-treatment), posttreatment, and at 6-months follow-up.
The results demonstrated a differential response in sarcoma, characterized by increasing left-ventricular (LV) mass and decreasing right ventricular ejection fraction (RVEF). In all patients, left ventricular ejection fraction (LVEF) remained > 50% at all timepoints. Myocardial strain was always lower than the normal threshold values and showed small changes between different timepoints. Myocardial T2 and extracellular volume (ECV) showed increasing and decreasing patterns, respectively, in sarcoma, which were the opposite patterns of those in breast cancer. While myocardium T1 showed increasing values in breast cancer, T1 in sarcoma increased post-treatment and then decreased at the 6-months follow-up. The results showed inverse correlation between dose and different strain components in sarcoma, which was not the case in breast cancer. Certain myocardial segments showed high correlation coefficients with dose, which may reflect their increased sensitivity to cardiotoxicity.
Cardiac MRI proved to be a valuable technique for determining anthracycline-induced changes in cardiac function and myocardial tissue composition in sarcoma and differentiating it against breast cancer. It also provides a comprehensive assessment of heart health at baseline, which is important for risk stratification.
在过去几十年中,许多研究聚焦于蒽环类药物对心脏的影响(心脏毒性),但仅有少数研究关注肉瘤。在本研究中,我们利用先进的心脏磁共振成像(MRI)技术来表征蒽环类药物诱发的肉瘤心脏毒性,并将结果与乳腺癌患者的结果进行比较。
患者在三个时间点接受MRI检查:基线(治疗前)、治疗后以及6个月随访时。
结果显示肉瘤存在不同的反应,其特征为左心室(LV)质量增加和右心室射血分数(RVEF)降低。在所有患者中,左心室射血分数(LVEF)在所有时间点均保持>50%。心肌应变始终低于正常阈值,且在不同时间点之间变化较小。肉瘤患者的心肌T2和细胞外容积(ECV)分别呈现增加和减少的模式,这与乳腺癌患者的模式相反。乳腺癌患者中,心肌T1值升高,而肉瘤患者的T1值在治疗后升高,随后在6个月随访时降低。结果显示肉瘤中剂量与不同应变成分之间呈负相关,而乳腺癌并非如此。某些心肌节段与剂量的相关系数较高,这可能反映了它们对心脏毒性的敏感性增加。
心脏MRI被证明是一种有价值的技术,可用于确定蒽环类药物诱发的肉瘤心脏功能和心肌组织成分变化,并与乳腺癌进行区分。它还能在基线时对心脏健康进行全面评估,这对风险分层很重要。