Bria Emilio, Cuppone Federica, Milella Michele, Verma Sunil, Carlini Paolo, Nisticò Cecilia, Vaccaro Vanja, Rossi Antonio, Tonini Giuseppe, Cognetti Francesco, Terzoli Edmondo
Regina Elena National Cancer Institute, Department of Medical Oncology, Via Elio Chianesi 53, 00144, Rome, Italy.
Expert Opin Biol Ther. 2008 Dec;8(12):1963-71. doi: 10.1517/14728220802517935.
Trastuzumab has significantly improved the prognosis of breast cancer patients overexpressing the human epidermal growth factor receptor 2 (HER2). This result has been achieved in all disease settings, by increasing overall survival in early stage and advanced disease and by increasing pathological complete responses in neoadjuvant disease.
Although the greatest impact of this monoclonal antibody has been seen in the adjuvant setting, by increasing disease-free survival and overall survival rates an increased rate of both symptomatic and non-symptomatic cardiac toxicity has also been observed.
In the following review, the different mechanisms of trastuzumab cardiac toxicity are described and, in addition, the clinical data coming from both trials and meta-analyses is discussed.
While there is strong evidence for the incidence of trastuzumab-related cardiac toxicity, there is still little known on the exact pathogenesis of this toxicity. Interestingly, both experimental and clinical data suggest that trastuzumab may sensitize cardiomyocytes to injuries and stress from administration of anthracyclines. This has led to a proposed novel mechanism of cardiotoxicity that appears to be quite different from the anthracycline-associated cardiotoxicity. Trastuzumab does not seem to cause any overt ultrastructural abnormality; it does, however, lead to myocardial dysfunction.
Most of the proposed hypotheses seems to be related to the activity of trastuzumab in interfering with the ERBB-2 receptor. Indeed, data from clinical trials in the adjuvant setting report increased cardiac toxicity in those patients who previously received anthracyclines.
曲妥珠单抗显著改善了过表达人表皮生长因子受体2(HER2)的乳腺癌患者的预后。在所有疾病阶段均取得了这一成果,包括提高早期和晚期疾病的总生存率以及增加新辅助治疗疾病的病理完全缓解率。
尽管这种单克隆抗体在辅助治疗中产生了最大影响,提高了无病生存率和总生存率,但也观察到有症状和无症状心脏毒性的发生率有所增加。
在以下综述中,描述了曲妥珠单抗心脏毒性的不同机制,此外,还讨论了来自试验和荟萃分析的临床数据。
虽然有充分证据证明曲妥珠单抗相关心脏毒性的发生率,但对这种毒性的确切发病机制仍知之甚少。有趣的是,实验和临床数据均表明,曲妥珠单抗可能使心肌细胞对蒽环类药物给药引起的损伤和应激敏感。这导致了一种新提出的心脏毒性机制,该机制似乎与蒽环类药物相关的心脏毒性有很大不同。曲妥珠单抗似乎不会引起任何明显的超微结构异常;然而,它确实会导致心肌功能障碍。
大多数提出的假设似乎与曲妥珠单抗干扰ERBB-2受体的活性有关。事实上,辅助治疗临床试验的数据报告显示,先前接受过蒽环类药物治疗的患者心脏毒性增加。