Department of Pediatric Oncology, Emma Children's Hospital/Academic Medical Center, Amsterdam, the Netherlands.
Pediatr Blood Cancer. 2010 Apr;54(4):579-84. doi: 10.1002/pbc.22371.
Exercise echocardiography reveals abnormalities in asymptomatic childhood cancer survivors who previously have been treated with anthracyclines. We determined the added value of monitoring childhood cancer survivors with exercise echocardiography compared to monitoring with resting echocardiography alone to predict anthracycline-induced cardiotoxicity. Secondary aims were to evaluate change in resting cardiac function over 10 years and to determine risk factors for late cardiotoxicity.
We invited a cohort of 110 originally asymptomatic anthracycline-treated childhood cancer survivors, who had undergone cardiac tests including exercise echocardiography 10.5 years earlier, for new cardiac evaluation. Each subject underwent a resting echocardiogram at both evaluations. At first evaluation a repeat echocardiogram was performed following peak exercise. Resting echocardiographic parameters were converted to z-character.
Ninety-two of 110 survivors (mean anthracycline dose 307 mg/m(2), mean follow-up time from start of treatment 8.2 years at first and 18.8 years at second evaluation) were evaluated prospectively. Mean resting fractional shortening z-character (RFSz) decreased from -0.18 to -0.93. Higher cumulative anthracycline dose was a risk factor for a lower RFSz at late follow-up (P = 0.0002). Adding exercise fractional shortening (XFS) to a model containing RFSz did not improve prediction of abnormal RFSz at late follow-up.
Monitoring with exercise echocardiography has no added value to monitoring with resting echocardiography alone in predicting late anthracycline-induced cardiotoxicity in childhood cancer survivors. RFSz deteriorates over time, even in originally asymptomatic patients. Previous treatment with higher cumulative anthracycline dose is the main risk factor for a lower RFSz at late follow-up.
运动超声心动图揭示了既往接受蒽环类药物治疗的无症状儿童癌症幸存者的异常。我们确定了运动超声心动图监测与单独静息超声心动图监测相比,预测蒽环类药物诱导的心脏毒性的附加价值。次要目的是评估 10 年内静息心功能的变化,并确定晚期心脏毒性的危险因素。
我们邀请了一组 110 名原本无症状的蒽环类药物治疗的儿童癌症幸存者,他们在 10.5 年前接受了包括运动超声心动图在内的心脏检查,进行新的心脏评估。每位患者在两次评估时都接受了静息超声心动图检查。在第一次评估时,在达到峰值运动后进行重复超声心动图检查。将静息超声心动图参数转换为 z 特征。
在 110 名幸存者中,有 92 名(平均蒽环类药物剂量为 307mg/m2,从开始治疗到第一次和第二次评估的平均随访时间分别为 8.2 年和 18.8 年)进行了前瞻性评估。平均静息分数缩短 z 特征(RFSz)从-0.18 降至-0.93。较高的累积蒽环类药物剂量是晚期随访时 RFSz 较低的危险因素(P=0.0002)。在包含 RFSz 的模型中添加运动分数缩短(XFS)并不能改善晚期预测异常 RFSz 的能力。
在预测儿童癌症幸存者晚期蒽环类药物诱导的心脏毒性方面,运动超声心动图监测与单独静息超声心动图监测相比没有额外价值。RFSz 随时间恶化,即使在最初无症状的患者中也是如此。以前接受较高累积蒽环类药物剂量是晚期随访时 RFSz 较低的主要危险因素。