Chong Esther G, Lee Eric H, Sail Reena, Denham Laura, Nagaraj Gayathri, Hsueh Chung-Tsen
Department of Medicine, Loma Linda University, Loma Linda, CA 92350, United States.
Department of Hematology/Oncology, Compassionate Cancer Care Medical Group, Fountain Valley, CA 92708, United States.
World J Cardiol. 2021 Jan 26;13(1):28-37. doi: 10.4330/wjc.v13.i1.28.
Doxorubicin and other anthracycline derivatives inhibit topoisomerase II and is an important class of cytotoxic chemotherapy in cancer treatment. The use of anthracycline is limited by dose-dependent cardiotoxicity, which may manifest initially as asymptomatic cardiac dysfunction with subsequent progression to congestive heart failure. Despite baseline assessment and periodic monitoring of cardiac function for patients receiving anthracycline agents, there are unmet needs in prediction and prevention of anthracycline-induced cardiotoxicity (AIC).
A 35-year-old African American female was found to have a 9-cm high-grade osteosarcoma of right femur and normal baseline cardiac function with left ventricular ejection fraction of approximately 60%-70% determined by transthoracic and dobutamine stress echocardiogram. She underwent perioperative doxorubicin and cisplatin chemotherapy with 3 cycles before surgery and 3 cycles after surgery, and received a total of 450 mg/m doxorubicin at the end of her treatment course. She was evaluated regularly during chemotherapy without any cardiac or respiratory symptoms. Approximately two months after her last chemotherapy, the patient presented to the emergency department with dyspnea for one week and was intubated for acute hypoxic respiratory failure. Echocardiogram showed an ejection fraction of 5%-10% with severe biventricular failure. Despite attempts to optimize cardiac function, the patient's hemodynamic status continued to decline, and resuscitation was not successful on the seventh day of hospitalization. The autopsy showed no evidence of osteosarcoma, and the likely cause of death was cardiac failure with the evidence of pulmonary congestion, liver congestion, and multiple body cavity effusions.
We present a case of 35-year-old African American female developing cardiogenic shock shortly after receiving a cumulative dose of 450 mg/m doxorubicin over 9 mo. Cardiac monitoring and management of patients receiving anthracycline chemotherapy have been an area of intense research since introduction of these agents in clinical practice. We have reviewed literature and recent advances in the prediction and prevention of AIC. Although risk factors currently identified can help stratify patients who need closer monitoring, there are limitations to our current understanding and further research is needed in this field.
多柔比星及其他蒽环类衍生物可抑制拓扑异构酶II,是癌症治疗中一类重要的细胞毒性化疗药物。蒽环类药物的使用受剂量依赖性心脏毒性的限制,其最初可能表现为无症状性心脏功能障碍,随后进展为充血性心力衰竭。尽管对接受蒽环类药物治疗的患者进行了心脏功能的基线评估和定期监测,但在预测和预防蒽环类药物所致心脏毒性(AIC)方面仍存在未满足的需求。
一名35岁非裔美国女性被发现患有右股骨9厘米高分级骨肉瘤,经胸及多巴酚丁胺负荷超声心动图测定其基线心脏功能正常,左心室射血分数约为60%-70%。她在围手术期接受了多柔比星和顺铂化疗,术前3个周期,术后3个周期,治疗疗程结束时共接受了450mg/m²的多柔比星。化疗期间她接受了定期评估,未出现任何心脏或呼吸症状。在她最后一次化疗后约两个月,患者因呼吸困难一周就诊于急诊科,因急性低氧性呼吸衰竭行气管插管。超声心动图显示射血分数为5%-10%,伴有严重的双心室衰竭。尽管尝试优化心脏功能,但患者的血流动力学状态持续下降,住院第七天复苏未成功。尸检未发现骨肉瘤证据,可能的死亡原因是心力衰竭,伴有肺充血、肝充血和多浆膜腔积液的证据。
我们报告了一例35岁非裔美国女性在9个月内累积接受450mg/m²多柔比星后不久发生心源性休克的病例。自从这些药物引入临床实践以来,接受蒽环类化疗患者的心脏监测和管理一直是一个深入研究的领域。我们回顾了关于AIC预测和预防的文献及最新进展。尽管目前确定的危险因素有助于对需要密切监测的患者进行分层,但我们目前的认识存在局限性,该领域需要进一步研究。