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首页> 外文期刊>The breast journal >Trastuzumab‐related cardiotoxicity in patients with nonlimiting cardiac comorbidity
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Trastuzumab‐related cardiotoxicity in patients with nonlimiting cardiac comorbidity

机译:非限制性心脏合并症患者的曲妥珠猴与相关的心脏毒性

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Abstract Background Significant and symptomatic cardiac comorbidity is a contraindication to adjuvant trastuzumab in breast cancer patients. However, some patients with asymptomatic, nonlimiting cardiac comorbidity and normal baseline left ventricular ejection fraction (LVEF) receive adjuvant trastuzumab in the clinical practice. We sought to describe the tolerability of trastuzumab in these patients. Patients and Methods Retrospective analysis of patients with baseline asymptomatic, nonlimiting cardiac comorbidity receiving adjuvant trastuzumab at six Institutions between July 2007 and January 2016. Results Thirty‐seven patients with HER2‐positive, surgery treated breast cancer at high risk of relapse were studied. Median age was 64?years (range 36‐82), median baseline LVEF 61% (range 50%‐85%). Thirteen patients (35%) received trastuzumab with adjuvant anthracycline and taxane‐based regimens, 19 (51%) with taxane‐based, three (8%) with off‐label vinorelbine and two (5%) with off‐label endocrine therapy. Most frequent cardiac comorbidities were ischemic heart disease (35%), valvular disease (30%), atrial fibrillation (19%), and conduction disorders (14%). Nine patients (24.3%) experienced a cardiac event: congestive heart failure (one patient, 3%), asymptomatic LVEF reduction (six patients, 16%), and rhythm disturbances (two patients, 5%). Trastuzumab had to be discontinued either permanently (five patients, 14%) or temporarily (two patients, 5%). At the time of last follow‐up visit, all patients showed LVEF within normal limits, except one who had experienced a symptomatic cardiac event (LVEF value at last follow‐up 46%). Conclusions Caution is needed in patients with significant ongoing cardiovascular risk factors, but when adjuvant trastuzumab is deemed beneficial on breast cancer outcomes, nonlimiting cardiac comorbidity should not preclude treatment.
机译:摘要背景显着症状心脏合并是乳腺癌患者佐剂曲妥珠单抗的禁忌症。然而,一些无症状,非限制性的心脏合并和正常基线左心室喷射部分(LVEF)的患者在临床实践中接受佐剂曲据。我们试图描述这些患者中曲妥珠单抗的可耐受性。 2007年7月和2016年1月六个机构基线无线性,非限制性心脏合并患者患者的患者及方法回顾性分析。结果,研究了三十七名HER2阳性,患有高拷贝风险的乳腺癌患者。中位年龄为64岁?年(范围36-82),中位数基线LVEF 61%(范围50%-85%)。 13名患者(35%)接受了曲妥珠单抗与佐剂的蒽环类,19名(51%),19(51%),以紫杉烷的三(8%),其中偏离标记的血列和两(5%),具有偏离标签内分泌治疗。最常见的心脏伴有缺血性心脏病(35%),瓣膜疾病(30%),心房颤动(19%)和导电疾病(14%)。九名患者(24.3%)经历了心脏事件:充血性心力衰竭(一名患者,3%),无症状的持平(六名患者,16%)和节奏干扰(两名患者,5%)。曲妥珠单抗必须永久停产(五名患者,14%)或暂时(两名患者,5%)。在上次进行后续访问时,所有患者均在正常限制内显示出LVEF,除了经历症状心脏事件的人(最后一次随访46%的LVEF值)。结论患者患有明显的心血管危险因素的患者需要注意,但是当佐剂曲妥珠单抗被视为对乳腺癌结果有益时,非目的心脏合并症不宜妨碍治疗。

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