Khan Muhammad F, Gottesman Silvija, Boyella Ravichandra, Juneman Elizabeth
Department of Medicine, Southern Arizona VA Health Care System, 3601 South 6th Avenue (SAVAHCS, 1-11C), Tucson, AZ 85723, USA.
J Med Case Rep. 2014 Jun 23;8:220. doi: 10.1186/1752-1947-8-220.
Newly developed antineoplastic drugs have resulted in improvements in morbidity and mortality from many forms of cancers. However, some of these new chemotherapeutic agents have potentially lethal side effects, which are now being exposed with their widespread use. Gemcitabine is a nucleoside analog, which is a commonly used agent for various solid organ malignancies. Phase 1 and 2 trials with gemcitabine did not show significant risk for cardiotoxicity; however, with its widespread clinical use over the last decade, a few cases of cardiotoxicity related to gemcitabine use have been reported. Cardiomyopathy after the use of gemcitabine monotherapy is extremely rare; and only one such case has been reported in detail previously.
We report a case of a 56-year-old African American man with pancreatic cancer who presented with signs and symptoms of congestive heart failure after being treated with gemcitabine for two cycles (six doses). A two-dimensional echocardiography showed left ventricular ejection fraction of 15 to 20 percent with global hypokinesia. With the absence of significant risk factors for coronary artery disease and a strong temporal relationship with the initiation of chemotherapy, it was concluded that our patient's cardiomyopathy was related to the use of gemcitabine. Gemcitabine was discontinued and our patient responded well to standard heart failure therapy. Two months later, a repeat echocardiogram showed significant improvements in left ventricular systolic function.
Gemcitabine should be considered as a potential cause of cardiomyopathy in patients receiving chemotherapy with this drug. We need further studies to look into potential mechanisms and treatments of gemcitabine-induced cardiac dysfunction.
新研发的抗肿瘤药物已使多种癌症的发病率和死亡率有所改善。然而,其中一些新型化疗药物具有潜在的致命副作用,随着它们的广泛使用,这些副作用如今正逐渐显现出来。吉西他滨是一种核苷类似物,是用于治疗各种实体器官恶性肿瘤的常用药物。吉西他滨的1期和2期试验未显示出明显的心脏毒性风险;然而,在过去十年其临床广泛应用后,已有一些与使用吉西他滨相关的心脏毒性病例报道。使用吉西他滨单药治疗后发生的心肌病极为罕见;此前仅详细报道过1例此类病例。
我们报告1例56岁非裔美国男性胰腺癌患者,在用吉西他滨治疗两个周期(六剂)后出现充血性心力衰竭的体征和症状。二维超声心动图显示左心室射血分数为15%至20%,伴有整体运动减弱。由于不存在冠状动脉疾病的显著危险因素,且与化疗开始有很强的时间关联,得出结论认为我们患者的心肌病与使用吉西他滨有关。停用吉西他滨后,我们的患者对标准心力衰竭治疗反应良好。两个月后,重复超声心动图显示左心室收缩功能有显著改善。
对于接受吉西他滨化疗的患者,应将吉西他滨视为心肌病的潜在病因。我们需要进一步研究以探究吉西他滨诱导的心脏功能障碍的潜在机制和治疗方法。