Hasnie Ammar, Neace Zachary, Ellison Kristin, Hesselson Aaron, Ayoub Karam, Al-Yafi Mohammed, Arbune Amit
Department of Cardio-Oncology, Gill Heart & Vascular Institute, University of Kentucky, Lexington, KY, United States.
Front Cardiovasc Med. 2025 Sep 9;12:1594338. doi: 10.3389/fcvm.2025.1594338. eCollection 2025.
Intravenous 5-fluorouracil (5-FU), in combination with oxaliplatin and folinic acid, makes up a chemotherapy regimen commonly referred to as FOLFOX. It is well-established for its efficacy in patients with advanced colorectal cancer; however, the benefits are accompanied by potential side effects that warrant careful consideration. Common toxicities can range from nausea and vomiting to neuropathy. Cardiotoxicities related to FOLFOX and fluoropyrimidines in general are extremely rare but can easily be fatal.
A 41-year-old woman who was recently diagnosed with stage IIIc colorectal cancer after she underwent a subtotal colectomy was admitted to the Oncology clinic for further treatment. Given her excellent performance status and lack of comorbidities, she was started on adjuvant FOLFOX therapy. Three days after her first dose, she presented to the emergency room with several episodes of self-limited substernal chest pain. An electrocardiogram was performed, which showed ST-segment elevation concerning for acute myocardial infarction. She was taken emergently for a coronary angiogram, which revealed no evidence of obstructive coronary artery disease or spontaneous coronary artery dissection. Her presentation was most consistent with coronary vasospasm secondary to her recently started chemotherapy regimen. She was monitored in the cardiac critical care unit; the next day, she developed a breakthrough chest pain and subsequently developed polymorphic ventricular tachycardia with loss of consciousness. It was found that she had suffered a breakthrough coronary vasospasm precipitating a life-threatening arrhythmia. She was started on calcium channel blockers and nitrates with the aim of preventing further episodes of her hypersensitivity-induced vasospasm, and she was eventually successfully rechallenged with a Nordic FLOX bolus-based regimen.
In an unusual fashion, our patient developed ST-segment elevation myocardial infarction (STEMI) caused by coronary vasospasm, followed by delayed polymorphic ventricular tachycardia approximately 24 h later. This dual-phase presentation and subsequent successful rechallenge with bolus-based 5-FU chemotherapy have not been previously reported.
静脉注射5-氟尿嘧啶(5-FU)联合奥沙利铂和亚叶酸组成了一种通常称为FOLFOX的化疗方案。其在晚期结直肠癌患者中的疗效已得到充分证实;然而,这些益处伴随着一些需要仔细考虑的潜在副作用。常见毒性从恶心、呕吐到神经病变不等。一般而言,与FOLFOX和氟嘧啶相关的心脏毒性极为罕见,但可能轻易致命。
一名41岁女性,在接受次全结肠切除术后最近被诊断为IIIc期结直肠癌,入住肿瘤门诊接受进一步治疗。鉴于其良好的身体状况且无合并症,她开始接受辅助FOLFOX治疗。首次给药三天后,她因多次发作自限性胸骨后胸痛前往急诊室。进行了心电图检查,显示ST段抬高,提示急性心肌梗死。她被紧急送往进行冠状动脉造影,结果显示没有阻塞性冠状动脉疾病或自发性冠状动脉夹层的证据。她的表现最符合继发于其最近开始的化疗方案的冠状动脉痉挛。她在心脏重症监护病房接受监测;第二天,她出现了突破性胸痛,随后发展为多形性室性心动过速并伴有意识丧失。发现她发生了突破性冠状动脉痉挛,引发了危及生命的心律失常。她开始使用钙通道阻滞剂和硝酸盐,以预防其超敏反应性血管痉挛的进一步发作,最终她成功地再次接受了基于北欧FLOX推注的方案治疗。
以一种不同寻常的方式,我们的患者发生了由冠状动脉痉挛引起的ST段抬高型心肌梗死(STEMI),随后在大约24小时后出现了延迟性多形性室性心动过速。这种双相表现以及随后成功再次接受基于推注的5-FU化疗此前尚未见报道。