Tang Xue-Miao, Chen Hao, Li Qing, Song Yiling, Zhang Shuping, Xu Xiao-Shuan, Xu Yiwei, Chen Shulin
Department of Ultrasound and Electrocardiogram.
State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Onco Targets Ther. 2017 Dec 28;11:123-129. doi: 10.2147/OTT.S149716. eCollection 2018.
The cardiac safety of cetuximab and panitumumab, particularly as single agents, has not been investigated extensively. This trial was designed to specifically evaluate the cardiac safety of cetuximab and panitumumab as single therapy in Chinese chemotherapy-refractory metastatic colorectal cancer (mCRC) patients.
Sixty-one patients received cetuximab at an initial dose of 400 mg/m intravenously over 120 minutes on day 1 (week 1), followed by a maintenance dose of 250 mg/m intravenously over 60 minutes on day 1 of each 7-day cycle. Forty-three patients received panitumumab at a dose of 6 mg/kg intravenously every 14 days. Routine laboratory tests and electrocardiogram (ECG) were performed at baseline, during therapy and after the treatment (4th and 10th months). The incidence of elevation of troponin I ultra (TNI Ultra), abnormal ECGs, cardiac events and noncardiac adverse events (AEs) were recorded and analyzed.
The incidence of elevation of TNI Ultra between the two groups had no significance (=0.681), and TNI Ultra+ was observed more frequently in patients with metastases to more than three organs and they received fourth or above lines of chemotherapy. The most frequent abnormal ECG manifestations were nonspecific ST changes and QTc prolongation in the two groups. At 10 months after treatment, most of the abnormal ECG manifestations were reversed. The most common cardiac AEs of cetuximab and panitumumab included palpitations, dyspnea, chest pain and arrhythmias requiring treatment. Most of the events were mild and transient. The incidence of cardiac AEs had no significant difference between the two groups. Rash was still the most common noncardiac AE in both groups.
Cetuximab and panitumumab showed favorable cardiac safety as single agents for Chinese chemotherapy-refractory mCRC patients. But monitoring for cardiac AEs is still necessary throughout the entire treatment process.
西妥昔单抗和帕尼单抗的心脏安全性,尤其是作为单药治疗时,尚未得到广泛研究。本试验旨在专门评估西妥昔单抗和帕尼单抗作为单药疗法对中国化疗难治性转移性结直肠癌(mCRC)患者的心脏安全性。
61例患者在第1天(第1周)静脉滴注初始剂量为400mg/m²的西妥昔单抗,持续120分钟,随后在每7天周期的第1天静脉滴注维持剂量为250mg/m²,持续60分钟。43例患者每14天静脉滴注剂量为6mg/kg的帕尼单抗。在基线期、治疗期间及治疗后(第4个月和第10个月)进行常规实验室检查和心电图(ECG)检查。记录并分析超敏肌钙蛋白I(TNI Ultra)升高、心电图异常、心脏事件及非心脏不良事件(AE)的发生率。
两组间TNI Ultra升高的发生率无显著性差异(P = 0.681),在转移至三个以上器官且接受过四线及以上化疗的患者中更频繁观察到TNI Ultra升高。两组中最常见的心电图异常表现为非特异性ST段改变和QTc延长。治疗10个月后,大多数心电图异常表现恢复正常。西妥昔单抗和帕尼单抗最常见的心脏AE包括心悸、呼吸困难、胸痛及需要治疗的心律失常。大多数事件为轻度且短暂性。两组间心脏AE的发生率无显著差异。皮疹仍是两组中最常见的非心脏AE。
对于中国化疗难治性mCRC患者,西妥昔单抗和帕尼单抗作为单药显示出良好的心脏安全性。但在整个治疗过程中仍有必要监测心脏AE。