Department of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Department of Oncology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Acta Oncol. 2021 Apr;60(4):475-481. doi: 10.1080/0284186X.2020.1842904. Epub 2020 Nov 16.
Overall survival has improved significantly in patients with human epidermal growth receptor 2 (HER2)-positive breast cancer due to the use of the monoclonal antibody trastuzumab blocking HER2. However, patients may develop trastuzumab-induced cardiotoxicity (TIC) leading to congestive heart failure. Here we assessed whether analysing NT-proBNP and assessment of electrocardiography (ECG) could detect TIC during trastuzumab therapy.
One hundred thirty-six patients undergoing adjuvant, neoadjuvant or palliative chemotherapy and HER2 blockade for HER2-positive breast cancer were prospectively assessed with echocardiography, ECG and N-terminal - pro hormone B-type natriuretic peptide (NT-proBNP) testing at baseline and at 6 and 12 months of trastuzumab therapy. TIC was defined as a left ventricular ejection fraction (LVEF) of less than 50% and a decline from baseline of ≥10 units.
Six patients developed TIC under 12 months of trastuzumab therapy (incidence 4.4%). NT-proBNP increased from 198.8 ± 64.0 pg/ml to 678.7 ± 132.4 pg/ml ( < .05) in TIC patients. With a cut-off point of 276.5 pg/ml for NTproBNP and increase in NT-proBNP by 75.8 pg/ml from baseline the sensitivity was 100% and the specificity 95% to detect TIC. Compared with controls, TIC patients were older (68.3 ± 1.1 years and 56.2 ± 1.4 years, respectively; < .01), had more often diabetes mellitus (OR = 63.5, 95% CI: 5.63-915, < .01) and atrial fibrillation (OR = 12.3; 95% CI: 1.89-74.62; < .05) and had lower baseline LVEF (57.1 ± 1.4% and 61.4 ± 0.3%, respectively; < .001). Abnormal ECGs were common in patients developing TIC.
Measuring changes in NTproBNP may be used to monitor patients for TIC under trastuzumab therapy. Patients with a cardiovascular risk profile are more at risk of developing TIC.
由于使用单克隆抗体曲妥珠单抗阻断 HER2,人表皮生长因子受体 2(HER2)阳性乳腺癌患者的总生存率显著提高。然而,患者可能会发生曲妥珠单抗诱导的心脏毒性(TIC),导致充血性心力衰竭。在这里,我们评估了分析 NT-proBNP 和心电图(ECG)是否可以在曲妥珠单抗治疗期间检测 TIC。
136 名接受辅助、新辅助或姑息化疗和曲妥珠单抗治疗 HER2 阳性乳腺癌的患者接受前瞻性评估,包括基线和曲妥珠单抗治疗 6 个月和 12 个月时的超声心动图、心电图和 N 端 - 前激素 B 型利钠肽(NT-proBNP)检测。TIC 定义为左心室射血分数(LVEF)<50%和基线下降≥10 个单位。
6 名患者在曲妥珠单抗治疗 12 个月内发生 TIC(发生率 4.4%)。TIC 患者的 NT-proBNP 从 198.8±64.0pg/ml 增加到 678.7±132.4pg/ml( < .05)。NT-proBNP 的截断点为 276.5pg/ml,NT-proBNP 从基线增加 75.8pg/ml,其敏感性为 100%,特异性为 95%,以检测 TIC。与对照组相比,TIC 患者年龄更大(分别为 68.3±1.1 岁和 56.2±1.4 岁; < .01),更常患有糖尿病(OR=63.5,95%CI:5.63-915; < .01)和心房颤动(OR=12.3;95%CI:1.89-74.62; < .05),且基线 LVEF 较低(分别为 57.1±1.4%和 61.4±0.3%; < .001)。心电图异常在发生 TIC 的患者中很常见。
测量 NT-proBNP 的变化可用于监测曲妥珠单抗治疗期间 TIC 的发生。具有心血管风险特征的患者更有可能发生 TIC。