Raza Hina, Javaid Mariyam, Rehman Wajiha, Rafiq Sana, Rashid Zermina, Shamim Rahat, Jaradat Abdolelah, Yousif Mohamed Deifallah
Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan.
Department of Health Informatics, Jazan University, Jazan, Saudi Arabia.
J Oncol Pharm Pract. 2024 Oct 3:10781552241275948. doi: 10.1177/10781552241275948.
5-Fluorouracil (5-FU) is a chemotherapeutic agent used to treat various types of cancers. Although widely used, it has consistently been attributed to cardiotoxicities after administration. The purpose of this study was to assess the parameters and predictors of cardiotoxicities associated with various 5-FU-based chemotherapeutic protocols in patients with GI/colorectal cancer, as well as the correlation of these cardiotoxic events with age, sex, cumulative dose, and risk factors such as obesity, hypertension, and family history of cardiac diseases.
A prospective study consisting of 396 patients of both sexes was conducted in the oncology ward of Nishtar Hospital in Multan, Pakistan. Patients were grouped according to the therapeutic protocol they received (5-FU monotherapy or in combination, with different dosing regimens). Electrocardiography and serum troponin levels were used to assess 5-FU-induced cardiotoxicity. In cases where cardiotoxicity was detected, 5-FU treatment was interrupted; nitroglycerin, nitrates, and calcium channel blockers were administered; and cardiac monitoring was initiated. 5-FU was discontinued in all cases of acute myocardial infarction.
Of the 396 patients, 28.5% reported different cardiotoxic symptoms after receiving various 5-FU-containing protocols. 35% had anginal pain, 13% suffered a myocardial infarction, 11% developed hypertension, and 10% presented heart failure. Patients receiving 5-FU combination therapy showed cardiotoxic events that were significantly different from those on 5-FU monotherapy. Based on the ECG results, only the QTc-d interval increased significantly (p < 0.001) after therapy. 68% of the patients had troponin levels > 2 ng/mL at the end of treatment.
Pre-existing cardiac diseases, treatment duration, smoking, and obesity were found to be influential components in the development of cardiotoxicity, and patients with cancer should be closely monitored during 5-FU chemotherapy.
5-氟尿嘧啶(5-FU)是一种用于治疗多种癌症的化疗药物。尽管其应用广泛,但给药后一直被认为会导致心脏毒性。本研究的目的是评估胃肠道/结直肠癌患者中与各种基于5-FU的化疗方案相关的心脏毒性参数和预测因素,以及这些心脏毒性事件与年龄、性别、累积剂量和肥胖、高血压、心脏病家族史等危险因素之间的相关性。
在巴基斯坦木尔坦尼什塔尔医院的肿瘤科病房对396名男女患者进行了一项前瞻性研究。患者根据所接受的治疗方案(5-FU单药治疗或联合治疗,采用不同的给药方案)进行分组。采用心电图和血清肌钙蛋白水平评估5-FU诱导的心脏毒性。在检测到心脏毒性的病例中,中断5-FU治疗;给予硝酸甘油、硝酸盐和钙通道阻滞剂,并开始心脏监测。在所有急性心肌梗死病例中停用5-FU。
在396名患者中,28.5%在接受各种含5-FU的方案后报告了不同的心脏毒性症状。35%有胸痛,13%发生心肌梗死,11%出现高血压,10%出现心力衰竭。接受5-FU联合治疗的患者出现的心脏毒性事件与接受5-FU单药治疗的患者有显著差异。根据心电图结果,治疗后仅QTc-d间期显著增加(p<0.001)。68%的患者在治疗结束时肌钙蛋白水平>2 ng/mL。
发现既往存在的心脏病、治疗持续时间、吸烟和肥胖是心脏毒性发生的影响因素,癌症患者在5-FU化疗期间应密切监测。