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表皮生长因子受体2靶向治疗的心脏毒性:我们了解多少?

Cardiac toxicity of ErbB2-targeted therapies: what do we know?

作者信息

Perez Edith A

机构信息

Division of Hematology/Oncology, Mayo Clinic, Jacksonville, FL 32224, USA.

出版信息

Clin Breast Cancer. 2008 Mar;8 Suppl 3:S114-20. doi: 10.3816/cbc.2008.s.007.

Abstract

The potential for cardiac toxicity in association with targeted biologic agents was first observed with trastuzumab, a monoclonal antibody that targets the ErbB2/HER2 receptor. In the pivotal trial of trastuzumab in ErbB2-positive metastatic cancer, an increased incidence of serious cardiac events was observed, particularly when trastuzumab was administered in combination with anthracyclines. The ErbB2 receptor is expressed on cardiomyocytes, in addition to tumor tissue, where it exerts a protective effect on cardiac function; thus, interference with ErbB2-signaling may block this protective effect. However, in contrast to anthracycline-induced cardiac toxicity, trastuzumab-related cardiac dysfunction does not appear to increase with cumulative dose or to be associated with ultrastructural changes in the myocardium and is generally reversible. When used in adjuvant regimens for the treatment of ErbB2-positive early-stage breast cancer, trastuzumab has been shown to significantly improve disease-free and overall survival. The incidence of class III/IV congestive heart failure (CHF) ranged from 0.4%-3.8% in the major adjuvant trastuzumab trials. More recently, small-molecule tyrosine kinase inhibitors such as lapatinib have been investigated for the treatment of ErbB2-positive metastatic breast cancer. In a comprehensive analysis of cardiac safety data from all lapatinib trials completed to date, which included 3558 healthy volunteers and patients with a variety of solid cancers on 43 trials, the overall incidence of left ventricular ejection fraction declines was 1.6%, with 0.2% of patients experiencing symptomatic CHF. Risk factors that might predict for cardiac dysfunction with ErbB2-targeted therapy are actively under investigation and will aid in the identification of at-risk populations and in the development of strategies for risk minimization in the future. It is important to note that, while careful cardiac monitoring is required for all patients receiving ErbB2-targeted therapy in any disease setting, the overall impact of these agents on the outcomes of patients with ErbB2-positive breast cancer has been dramatic and positive.

摘要

与靶向生物制剂相关的心脏毒性潜力最初是在曲妥珠单抗中观察到的,曲妥珠单抗是一种靶向表皮生长因子受体2(ErbB2/HER2)的单克隆抗体。在曲妥珠单抗用于ErbB2阳性转移性癌症的关键试验中,观察到严重心脏事件的发生率增加,尤其是当曲妥珠单抗与蒽环类药物联合使用时。除肿瘤组织外,ErbB2受体在心肌细胞上也有表达,在心肌细胞中它对心脏功能发挥保护作用;因此,干扰ErbB2信号传导可能会阻断这种保护作用。然而,与蒽环类药物引起的心脏毒性不同,曲妥珠单抗相关的心脏功能障碍似乎不会随着累积剂量的增加而增加,也与心肌的超微结构变化无关,并且通常是可逆的。当用于辅助治疗ErbB2阳性早期乳腺癌时,曲妥珠单抗已被证明能显著提高无病生存期和总生存期。在主要的曲妥珠单抗辅助试验中,III/IV级充血性心力衰竭(CHF)的发生率在0.4%-3.8%之间。最近,小分子酪氨酸激酶抑制剂如拉帕替尼已被研究用于治疗ErbB2阳性转移性乳腺癌。在对迄今为止完成的所有拉帕替尼试验的心脏安全性数据进行的综合分析中,这些试验包括3558名健康志愿者和43项试验中的各种实体癌患者,左心室射血分数下降的总体发生率为1.6%,0.2%的患者出现有症状的CHF。可能预测ErbB2靶向治疗心脏功能障碍的危险因素正在积极研究中,这将有助于识别高危人群,并在未来制定风险最小化策略。需要注意的是,虽然在任何疾病背景下接受ErbB2靶向治疗的所有患者都需要仔细的心脏监测,但这些药物对ErbB2阳性乳腺癌患者结局的总体影响是显著且积极的。

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