Division of Cardiology, Johns Hopkins Hospital, Baltimore, MD 21287, USA.
J Clin Oncol. 2010 Jul 20;28(21):3416-21. doi: 10.1200/JCO.2009.23.6950. Epub 2010 Jun 7.
An independent Adjuvant Cardiac Review and Evaluation Committee (ACREC) systematically reviewed cases of symptomatic heart failure events to uniformly define the cardiac event rate across two large trials (National Surgical Adjuvant Breast and Bowel Project [NSABP] B-31 and North Central Cancer Treatment Group [NCCTG] N9831) that assessed the addition of trastuzumab to standard adjuvant chemotherapy.
The committee was composed of six independent oncologists and cardiologists. A retrospective review of patients with a cardiac event was performed by the primary investigators of the trials. The ACREC prospectively established criteria for determining a symptomatic heart failure event. Recovery status was determined from documented resolution of signs and symptoms. Potential risk factors were also assessed.
Medical records for a total of 173 patients were reviewed: 40 in the chemotherapy-alone arm and 133 in the trastuzumab arm. Trastuzumab-treated patients had a 2.0% incidence of symptomatic heart failure events compared with 0.45% in the chemotherapy-alone arm. Complete or partial recovery was observed in 86.1% of trastuzumab-treated patients with symptomatic heart failure events. Of five patients who died, only one patient had received trastuzumab. Independent predictors for cardiac events were age older than 50 years, a low ejection fraction at the start of paclitaxel treatment, and trastuzumab treatment.
The incidence of symptomatic heart failure events is 2.0% in patients treated with adjuvant trastuzumab, and the majority of these patients recover with appropriate treatment.
独立的辅助心脏审查和评估委员会(ACREC)系统地审查了有症状心力衰竭事件的病例,以统一定义两个大型试验(国家外科辅助乳腺和肠道项目[NSABP] B-31 和中北部癌症治疗组[NCCTG] N9831)中曲妥珠单抗联合标准辅助化疗的心脏事件发生率。
该委员会由六名独立的肿瘤学家和心脏病学家组成。通过试验的主要研究者对发生心脏事件的患者进行了回顾性审查。ACREC 前瞻性地制定了确定有症状心力衰竭事件的标准。恢复状态根据记录的体征和症状的缓解来确定。还评估了潜在的危险因素。
共审查了 173 名患者的病历:化疗组 40 例,曲妥珠单抗组 133 例。与化疗组的 0.45%相比,曲妥珠单抗组有 2.0%的患者发生有症状的心力衰竭事件。接受曲妥珠单抗治疗的有症状心力衰竭事件患者中有 86.1%完全或部分恢复。在因心力衰竭事件死亡的五名患者中,只有一名患者接受了曲妥珠单抗治疗。心脏事件的独立预测因素是年龄大于 50 岁、紫杉醇治疗开始时射血分数低和曲妥珠单抗治疗。
接受辅助曲妥珠单抗治疗的患者发生有症状心力衰竭事件的发生率为 2.0%,大多数患者经适当治疗后可恢复。