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变形指标对曲妥珠单抗诱导心脏毒性预测的独立和增量价值。

Independent and incremental value of deformation indices for prediction of trastuzumab-induced cardiotoxicity.

机构信息

Heart and Vascular Institute, Cleveland Clinic, Cleveland, Ohio, USA.

出版信息

J Am Soc Echocardiogr. 2013 May;26(5):493-8. doi: 10.1016/j.echo.2013.02.008. Epub 2013 Apr 3.

Abstract

BACKGROUND

Assessment of left ventricular systolic function is necessary during trastuzumab-based chemotherapy because of potential cardiotoxicity. Deformation indices have been proposed as an adjunct to clinical risk factors and ejection fraction (EF), but the optimal parameter and optimal cutoffs are undefined. The aim of this study was to determine the best means of early detection of subsequent reduction of EF in patients with breast cancer treated with trastuzumab.

METHODS

Eighty-one consecutive women (mean age, 50 ± 11 years) receiving trastuzumab were prospectively studied, 37 of whom received concurrent anthracyclines. Conventional echocardiographic indices (mitral annular systolic [s'] and diastolic [e'] velocities) and myocardial deformation indices (global longitudinal peak systolic strain [GLS], global longitudinal peak systolic strain rate [GLSR-S], and global longitudinal early diastolic strain rate [GLSR-E]) were measured at baseline and at 6 and 12 months. Cardiotoxicity was defined as a >10% decline as a percentage of baseline EF in 12 months.

RESULTS

In the 24 patients (30%) who later developed cardiotoxicity, myocardial deformation indices decreased at 6 months (GLS, P < .001; GLSR-S, P = .009; GLSR-E, P = .002 vs baseline), but e' was unchanged. The strongest predictor of cardiotoxicity was ΔGLS (area under the curve, 0.84); an 11% reduction (95% confidence interval, 8.3%-14.6%) was the optimal cutoff, with sensitivity of 65% and specificity of 94%. In sequential models, the clinical model (χ(2) = 10.2) was improved by GLSR-S (χ(2) = 14.7, P = .03) and even more so by GLSR-E (χ(2) = 18.0, P = .005) or GLS (χ(2) = 21.3, P = .0008). Discrimination improvement by adding GLS was confirmed by an integrated discrimination improvement of 18.6% (95% confidence interval, 8.6%-28.6%; P = .0003). A net 29% of the patients without events were reclassified into lower risk categories, and a net 48% of the patients with events were reclassified into higher risk categories, resulting in a total continuous net reclassification improvement (>0) of 0.77 (95% confidence interval, 0.33-1.22; P = .036).

CONCLUSIONS

GLS is an independent early predictor of later reductions in EF, incremental to usual predictors in patients at risk for trastuzumab-induced cardiotoxicity.

摘要

背景

由于潜在的心毒性,曲妥珠单抗为基础的化疗期间需要评估左心室收缩功能。变形指数已被提议作为临床危险因素和射血分数(EF)的辅助手段,但最佳参数和最佳截断值尚未确定。本研究旨在确定在接受曲妥珠单抗治疗的乳腺癌患者中,早期检测 EF 随后降低的最佳方法。

方法

81 例连续接受曲妥珠单抗治疗的女性(平均年龄 50±11 岁)前瞻性研究,其中 37 例同时接受蒽环类药物治疗。在基线和 6 个月和 12 个月时测量常规超声心动图指标(二尖瓣环收缩期[s']和舒张期[e']速度)和心肌变形指数(整体纵向峰值收缩应变[GLS]、整体纵向峰值收缩应变率[GLSR-S]和整体纵向早期舒张应变率[GLSR-E])。心脏毒性定义为 12 个月内 EF 较基线下降>10%。

结果

在 24 例(30%)随后发生心脏毒性的患者中,心肌变形指数在 6 个月时下降(GLS,P<0.001;GLSR-S,P=0.009;GLSR-E,P=0.002 与基线相比),但 e'不变。心脏毒性的最强预测因子是ΔGLS(曲线下面积,0.84);11%的降幅(95%置信区间,8.3%-14.6%)为最佳截断值,其敏感性为 65%,特异性为 94%。在连续模型中,临床模型(χ²=10.2)通过 GLSR-S(χ²=14.7,P=0.03)得到改善,通过 GLSR-E(χ²=18.0,P=0.005)或 GLS(χ²=21.3,P=0.0008)得到的改善更为明显。通过增加 GLS 来改善鉴别力得到了确认,其综合鉴别力提高了 18.6%(95%置信区间,8.6%-28.6%;P=0.0003)。无事件的患者中有 29%被重新分类为低风险类别,有事件的患者中有 48%被重新分类为高风险类别,导致总连续净重新分类改善(>0)为 0.77(95%置信区间,0.33-1.22;P=0.036)。

结论

GLS 是 EF 随后降低的独立早期预测因子,在曲妥珠单抗诱导的心脏毒性风险患者中,增加了常规预测因子。

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