Milks M Wesley, Velez Michael R, Mehta Nishaki, Ishola Abiodun, Van Houten Thomas, Yildiz Vedat O, Reinbolt Raquel, Lustberg Maryam, Smith Sakima A, Orsinelli David A
Division of Cardiovascular Medicine, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Columbus Cardiology Consultants, Mount Carmel Health System, Columbus, Ohio.
Am J Cardiol. 2018 Apr 1;121(7):867-873. doi: 10.1016/j.amjcard.2017.12.022. Epub 2018 Jan 12.
The prediction of cancer therapeutics-related cardiac dysfunction (CTRCD) is an essential aspect of care for individuals who receive potentially cardiotoxic oncologic treatments. Certain clinical risk factors have been described for incident CTRCD, and measurement of left ventricular (LV) longitudinal strain by speckle tracking 2-dimensional echocardiography (2DE) is the best-validated myocardial mechanical imaging assessment to detect subtle changes in LV function during cancer treatment. However, the direct integration of clinical and imaging risk factors to predict CTRCD has not yet been extensively examined. This was a retrospective study of 183 women with breast cancer aged 50.9 ± 10.8 years who received treatment with anthracyclines (doxorubicin dose of 422 ± 69 mg/m, with 41.2% of subjects also receiving trastuzumab) and underwent 2DE at clinically determined intervals. CTRCD was diagnosed when LV ejection fraction dropped ≥10% to a subnormal (<53%) value by 2DE. Left ventricular global longitudinal strain (LV-GLS) was assessed offline. The risk prediction tool based only on clinical factors previously described by Ezaz et al was applied to our cohort and accurately stratified these subjects into low-, intermediate-, and high-risk groups, with incident CTRCD in 7.4%, 26.9%, and 54.6%, respectively (chi-square = 20.7, p <0.0001). We developed novel multivariate models to predict CTRCD using (1) demographic variables only (c = 0.8674), (2) echocardiographic (peak LV-GLS) variables only (c = 0.8440), or (3) a combination of demographic and echocardiographic variables, with the combined model exhibiting superior receiver-operating characteristics (c = 0.9629). In conclusion, estimation of CTRCD risk should integrate all available data, including both clinical variables and an imaging assessment.
癌症治疗相关心脏功能障碍(CTRCD)的预测是接受潜在心脏毒性肿瘤治疗患者护理的重要方面。已描述了某些CTRCD发病的临床风险因素,通过斑点追踪二维超声心动图(2DE)测量左心室(LV)纵向应变是检测癌症治疗期间LV功能细微变化的最佳验证心肌机械成像评估方法。然而,临床和成像风险因素直接整合以预测CTRCD尚未得到广泛研究。这是一项对183名年龄为50.9±10.8岁的乳腺癌女性进行的回顾性研究,这些女性接受了蒽环类药物治疗(多柔比星剂量为422±69mg/m,41.2%的受试者还接受了曲妥珠单抗治疗),并在临床确定的间隔时间接受了2DE检查。当2DE显示LV射血分数下降≥10%至低于正常(<53%)值时,诊断为CTRCD。离线评估左心室整体纵向应变(LV-GLS)。将Ezaz等人先前描述的仅基于临床因素的风险预测工具应用于我们的队列,并将这些受试者准确分层为低、中、高风险组,CTRCD发病率分别为7.4%、26.9%和54.6%(卡方检验=20.7,p<0.0001)。我们开发了新的多变量模型来预测CTRCD,使用(1)仅人口统计学变量(c=0.8674),(2)仅超声心动图(LV-GLS峰值)变量(c=0.8440),或(3)人口统计学和超声心动图变量的组合,联合模型表现出更好的受试者操作特征(c=0.9629)。总之,CTRCD风险评估应整合所有可用数据,包括临床变量和成像评估。