Cardiotoxicity of Anthracycline-based Chemotherapy in Breast Cancer Patients: A Case Series

Zhenisgul Sh. Tlegenova, Saule K. Balmagambetova, Bekolat K. Zholdin, Gulnara L. Kurmanalina, Iliada Zh. Talipova, Arip K. Koyshybaev, Gulmira A. Sultanbekova, Kulparshan I. Kubenova, Mira B. Baspayeva, Saule S. Madinova, Ayganym Amanova
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Abstract

In Kazakhstan, breast cancer (BC) remains the leading cause of cancer morbidity and mortality among women. The presented case series aims to summarize cardiovascular events that resulted in anthracycline-based chemotherapy discontinuation or suspension during the ongoing project on studying the cardiotoxicity effects. Case 1. Classic acute cardiotoxicity with asystole. Patient Sh., 46 years old, was admitted with a baseline LVEF of 64% and GLS of 22.4%. After the first dose of doxorubicin 60 mg/m2 and cyclophosphamide 600 mg/m2, the patient experienced two episodes of asystole. She was prescribed Trimetazidine at a dose of 80 mg. Eventually, Sh. completed the courses of anthracycline therapy after a 1-month delay at a cumulative dose of 455 mg/m2. Case 2. Subacute cardiotoxicity with ventricular extrasystole. Patient Zh., aged 47, developed single, paired, and group ventricular extrasystoles after the 2nd course of chemotherapy with doxorubicin 200 mg/m2 (23 days after admission). Carvedilol was prescribed at 25 mg twice daily and Trimetazidine at 80 mg once a day. After 1 month of monitoring, ventricular extrasystoles disappeared. With a month’s delay, the patient completed chemotherapy at a cumulative dose of 400 mg/m2. Case 3. Severe cardiotoxicity due to pre-existing cardiovascular disease with discontinuation of chemotherapy. Patient M., aged 58, was referred to the very highrisk group for developed atrial fibrillation and heart failure with LVEF 51%. M. received Enalapril 5 mg two times per day, Bisoprolol 5 mg, Eplerenone 50 mg, Dapagliflozin 10 mg, and Dabigatran 150 mg twice daily. After 3 months, anthracycline therapy was canceled at a cumulative dose of 260 mg/m2 due to the deterioration of the patient’s condition (LVEF 41%.). Discontinuation or the delay of vitally needed chemotherapy in BC patients deteriorate their prognosis for survival. Patients should be constantly monitored during and after anticancer treatment.
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乳腺癌患者接受蒽环类化疗的心脏毒性:病例系列
在哈萨克斯坦,乳腺癌(BC)仍然是妇女癌症发病率和死亡率的主要原因。本系列病例旨在总结在正在进行的心脏毒性影响研究项目中,导致蒽环类化疗中止或暂停的心血管事件。病例 1.典型的急性心脏毒性伴心搏骤停。患者 Sh. 46 岁,入院时基线 LVEF 为 64%,GLS 为 22.4%。在首次服用多柔比星 60 毫克/平方米和环磷酰胺 600 毫克/平方米后,患者出现了两次晕厥。医生给她开了 80 毫克剂量的曲美他嗪。最终,Sh.在推迟了 1 个月后完成了蒽环类药物治疗疗程,累计剂量为 455 毫克/平方米。病例 2.亚急性心脏毒性伴有室性期外收缩。患者 Zh,47 岁,在接受多柔比星 200 毫克/平方米化疗的第 2 个疗程后(入院后 23 天)出现单个、成对和成组室性期外收缩。医生为其开具了卡维地洛(25 毫克,每天两次)和曲美他嗪(80 毫克,每天一次)处方。经过一个月的监测,室性期外收缩消失了。延迟一个月后,患者完成了累积剂量为 400 毫克/平方米的化疗。病例 3.因原有心血管疾病导致严重心脏毒性而停止化疗。患者 M.,58 岁,因出现心房颤动和心力衰竭(LVEF 51%)而被转入极高风险组。M. 接受了依那普利 5 毫克、比索洛尔 5 毫克、依普利酮 50 毫克、达帕利嗪 10 毫克和达比加群 150 毫克的治疗,每天两次。3 个月后,由于患者病情恶化(LVEF 41%),取消了累计剂量为 260 毫克/平方米的蒽环类药物治疗。停止或推迟对 BC 患者进行急需的化疗会使其生存预后恶化。患者在接受抗癌治疗期间和之后都应接受持续监测。
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