Cardiotoxicity following different doses and schedules of 5-fluorouracil administration for malignancy -- a survey of 427 patients
- PMID: 12070449
Cardiotoxicity following different doses and schedules of 5-fluorouracil administration for malignancy -- a survey of 427 patients
Abstract
Background: Although cardiotoxicity associated with 5-Fluorouracil (5-FU) administration is infrequent, there are case reports of acute coronary syndromes. We report on patients undergoing 5-FU chemotherapy who developed cardiac symptoms during its administration.
Material/methods: In patients receiving 5-FU who experienced cardiac-related symptoms, ECG and serum cardiac enzyme determination were performed. If cardiotoxicity was detected, 5-FU infusion was interrupted, and the patients received sublingual nitrates and cardiac monitoring, while patients with more than 2-fold elevated enzyme levels were monitored in a coronary care unit for at least 72 hours. In cases of acute myocardial infarction, 5-FU was terminated.
Results: Of 427 patients entering the study, 17 (4%) developed clinical symptoms and ECG abnormalities indicating 5-FU cardiotoxicity. Patients with continuous infusion (c.i.) of 5-FU had a higher incidence of cardiotoxicity (12/197, 6%) than the remaining (5/235, 2.1%) (p=0.067), but more toxicity was encountered in patients with c.i. of 5-FU+LV for 24 hours for 5 days than in patients with the same regimen of 5-FU without LV (p<0.027) or patients with short 5-FU+LV administration (p=0.024). Seven of the 17 patients with 5-FU cardiotoxicity had an acute myocardial infarction, 4 developed ischemic changes, while 4 more patients had ECG abnormalities consistent with coronary vasospasm, of whom one subsequently died.
Conclusions: The present study supports the toxic effect of 5-FU on myocardium, which is largely schedule-dependent. Considerable vigilance is required when using this drug, and its toxic effect on the coronary endothelium and myocardium merit further investigation.
Similar articles
-
5-fluorouracil cardiotoxicity is a rare, dose and schedule-dependent adverse event: a prospective study.J BUON. 2005 Apr-Jun;10(2):205-11. J BUON. 2005. PMID: 17343330
-
Cardiotoxicity of fluoropyrimidines in different schedules of administration: a prospective study.J Cancer Res Clin Oncol. 2008 Jan;134(1):75-82. doi: 10.1007/s00432-007-0250-9. Epub 2007 Jul 17. J Cancer Res Clin Oncol. 2008. PMID: 17636329
-
Cardiotoxicity of de Gramont's regimen: incidence, clinical characteristics and long-term follow-up.Jpn J Clin Oncol. 2005 May;35(5):265-70. doi: 10.1093/jjco/hyi071. Epub 2005 Apr 26. Jpn J Clin Oncol. 2005. PMID: 15855175
-
Cardiotoxicity of 5-fluorouracil.Cancer Treat Rep. 1987 Jul-Aug;71(7-8):733-6. Cancer Treat Rep. 1987. PMID: 3300968 Review.
-
Fluoropyrimidine-associated cardiotoxicity: revisited.Expert Opin Drug Saf. 2009 Mar;8(2):191-202. doi: 10.1517/14740330902733961. Expert Opin Drug Saf. 2009. PMID: 19309247 Review.
Cited by
-
Cardio-oncology: a new and developing sector of research and therapy in the field of cardiology.Heart Fail Rev. 2019 Jan;24(1):91-100. doi: 10.1007/s10741-018-9731-y. Heart Fail Rev. 2019. PMID: 30073443 Review.
-
What the Cardiologist Needs to Consider in the Management of Oncologic Patients with STEMI-Like Syndrome: A Case Report and Literature Review.Pharmaceuticals (Basel). 2021 Jun 12;14(6):563. doi: 10.3390/ph14060563. Pharmaceuticals (Basel). 2021. PMID: 34204714 Free PMC article.
-
A systematic review of the pathophysiology of 5-fluorouracil-induced cardiotoxicity.BMC Pharmacol Toxicol. 2014 Sep 4;15:47. doi: 10.1186/2050-6511-15-47. BMC Pharmacol Toxicol. 2014. PMID: 25186061 Free PMC article. Review.
-
Treatment-Related Coronary Disorders of Fluoropyrimidine Administration: A Systematic Review and Meta-Analysis.Front Pharmacol. 2022 May 13;13:885699. doi: 10.3389/fphar.2022.885699. eCollection 2022. Front Pharmacol. 2022. PMID: 35645806 Free PMC article.
-
Penicillin allergy in cancer patients manifesting as Kounis syndrome.Heart Vessels. 2005 Jul;20(4):159-63. doi: 10.1007/s00380-004-0804-6. Heart Vessels. 2005. PMID: 16025365
MeSH terms
Substances
LinkOut - more resources
Full Text Sources