Lipshultz Steven E
Department of Pediatrics, and the Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
Semin Oncol. 2006 Jun;33(3 Suppl 8):S8-14. doi: 10.1053/j.seminoncol.2006.04.019.
The use of anthracyclines in the treatment of acute lymphoblastic leukemia is limited by associated cardiotoxic effects, which can result in cardiomyopathy and congestive heart failure, and may be irreversible. Anthracycline-induced cardiotoxicity in long-term survivors of childhood cancer is characterized by reduced left ventricular wall thickness and mass, which is indicative of decreased cardiac muscle and depressed left ventricular contractility which is indicative of unhealthy heart muscle. Risk factors for anthracycline-induced cardiotoxicity include high cumulative anthracycline doses, high anthracycline dose intensity, and radiotherapy. Radiotherapy in patients with cancer treated with anthracyclines can exacerbate anthracycline-induced cardiac tissue damage. Several studies have shown that cardiomyopathy disease progression can be delayed in adults by using angiotensin-converting enzyme inhibitors such as enalapril. Studies in long-term survivors of pediatric cancer showed that enalapril has significant benefits in preventing cardiac functional deterioration on a short-term basis, but this is not sustained. Anthracycline-associated cardiotoxic effects can be combatted by preventing cardiac injury during chemotherapy administration. There is evidence that dexrazoxane significantly reduces the cardiotoxicity associated with anthracyclines such as daunorubicin, doxorubicin, and epirubicin in adult patients with a wide range of tumor types. A study of the efficacy of dexrazoxane in reducing doxorubicin-induced cardiotoxicity in children and adolescents with high-risk acute lymphoblastic leukemia, showed that significantly fewer dexrazoxane-treated patients (21%) had elevated serum cardiac troponin (a biomarker of acute myocardial injury) levels than patients treated with chemotherapy alone (50%; P <.001). Dexrazoxane was also shown to have no effect on the event-free survival rate at 2.5 years, emphasizing that it does not detrimentally affect the efficacy of anthracycline therapy.
蒽环类药物在急性淋巴细胞白血病治疗中的应用受到相关心脏毒性作用的限制,这种毒性作用可导致心肌病和充血性心力衰竭,且可能是不可逆的。儿童癌症长期幸存者中蒽环类药物诱导的心脏毒性表现为左心室壁厚度和质量降低,这表明心肌减少,左心室收缩力降低,提示心肌不健康。蒽环类药物诱导的心脏毒性的危险因素包括高累积蒽环类药物剂量、高蒽环类药物剂量强度和放疗。接受蒽环类药物治疗的癌症患者进行放疗会加重蒽环类药物诱导的心脏组织损伤。多项研究表明,使用依那普利等血管紧张素转换酶抑制剂可延缓成人心肌病疾病进展。对儿科癌症长期幸存者的研究表明,依那普利在短期内预防心脏功能恶化方面有显著益处,但这种益处无法持续。在化疗给药期间预防心脏损伤可对抗蒽环类药物相关的心脏毒性作用。有证据表明,右丙亚胺可显著降低多种肿瘤类型的成年患者中与柔红霉素、多柔比星和表柔比星等蒽环类药物相关的心脏毒性。一项关于右丙亚胺在降低高危急性淋巴细胞白血病儿童和青少年中多柔比星诱导的心脏毒性疗效的研究表明,接受右丙亚胺治疗的患者(21%)血清心肌肌钙蛋白(急性心肌损伤的生物标志物)水平升高的人数明显少于单纯接受化疗的患者(50%;P<.001)。右丙亚胺还被证明对2.5年无事件生存率没有影响,这强调了它不会对蒽环类药物治疗的疗效产生不利影响。