Medicinal Safety Research Laboratories, Daiichi Sankyo Co, Ltd, Tokyo, Japan.
J Cardiovasc Pharmacol. 2022 Jan 1;79(1):e41-e49. doi: 10.1097/FJC.0000000000001157.
Treatment with trastuzumab, an antihuman epidermal growth factor receptor type 2 humanized monoclonal antibody, has been associated with heart failure in certain patients with cancer; however, the mechanism underlying trastuzumab-induced cardiac dysfunction remains unclear. This study was conducted to clarify the cardiac effects of trastuzumab in cynomolgus monkeys, which are commonly used as cross-reactive species in preclinical safety evaluation. Monkeys were treated with trastuzumab weekly for 1 month (5 doses in total). At first and fifth doses for pressure-volume loop analysis, trastuzumab at 20 mg·kg-1·10 min-1, equivalent to the human therapeutic dose, was administered intravenously to isoflurane-anesthetized animals, followed by 60 mg·kg-1·10 min-1 at a 30-minute interval. The other doses were fixed at 80 mg·kg-1·10 min-1 under unanesthetized conditions. After the first dose, reduced heart rate, decreases in maximal rate of fall of left ventricular pressure, and prolonged time constant for isovolumic relaxation, which are predictors of drug-induced changes in lusitropy, were observed at 20 and 60 mg·kg-1. The changes after the fifth dose were comparable with those after the first dose, indicating trastuzumab did not show exacerbation of cardiac function during the 1-month trial. No significant changes in slope of preload recruitable stroke work, which is a load-independent inotropic parameter, were observed at either dose. In conclusion, trastuzumab-induced little inotropic effect but induced negative chronotropic or lusitropic effects in monkeys, which might be associated with impaired left ventricular diastolic function.
曲妥珠单抗(一种抗人表皮生长因子受体 2 人源化单克隆抗体)的治疗与某些癌症患者的心力衰竭有关;然而,曲妥珠单抗诱导的心脏功能障碍的机制尚不清楚。本研究旨在阐明曲妥珠单抗在恒河猴中的心脏效应,恒河猴通常被用作临床前安全性评估中的交叉反应物种。猴子每周接受曲妥珠单抗治疗 1 个月(共 5 剂)。在压力-容积环分析的第一和第五剂量时,以 20mg·kg-1·10min-1(相当于人类治疗剂量)的速度静脉内给予异氟烷麻醉动物曲妥珠单抗,然后在 30 分钟间隔时给予 60mg·kg-1·10min-1。在未麻醉条件下,其他剂量固定在 80mg·kg-1·10min-1。在第一剂量后,在 20 和 60mg·kg-1 时观察到心率降低、左心室压力最大下降率降低以及等容舒张时间常数延长,这是药物引起的舒张性变化的预测指标。第五剂量后的变化与第一剂量后的变化相当,表明曲妥珠单抗在 1 个月的试验中没有表现出心脏功能的恶化。在任一剂量下,前负荷可诱导的射血工作斜率(一种非负荷性正性肌力参数)均无显著变化。总之,曲妥珠单抗对猴子的心肌收缩力影响较小,但引起负性变时或变力效应,这可能与左心室舒张功能受损有关。