Congestive heart failure in patients treated with doxorubicin: a retrospective analysis of three trials
- PMID: 12767102
- DOI: 10.1002/cncr.11407
Congestive heart failure in patients treated with doxorubicin: a retrospective analysis of three trials
Abstract
Background: Doxorubicin is a highly effective and widely used cytotoxic agent with application that is limited by cardiotoxicity related to the cumulative dose of the drug. A large-scale study that retrospectively evaluated the cardiotoxicity of doxorubicin reported that an estimated 7% of patients developed doxorubicin-related congestive heart failure (CHF) after a cumulative dose of 550 mg/m(2). To assess whether this estimate is reflective of the incidence in the broader clinical oncology setting, the authors evaluated data from three prospective studies to determine both the incidence of doxorubicin-related CHF and the accumulated dose of doxorubicin at which CHF occurs.
Methods: A group of 630 patients who were randomized to a doxorubicin-plus-placebo arm of three Phase III studies, two studies in patients with breast carcinoma and one study in patients with small cell lung carcinoma, were included in the analysis.
Results: Thirty-two of 630 patients had a diagnosis of CHF. Analysis indicated that an estimated cumulative 26% of patients would experience doxorubicin-related CHF at a cumulative dose of 550 mg/m(2). Age appeared to be an important risk factor for doxorubicin-related CHF after a cumulative dose of 400 mg/m(2), with older patients (age > 65 years) showing a greater incidence of CHF compared with younger patients (age < or = 65 years). In addition, > 50% of the patients who experienced doxorubicin-related CHF had a reduction < 30% in left ventricular ejection fraction (LVEF) while they were on study.
Conclusions: Doxorubicin-related CHF occurs with greater frequency and at a lower cumulative dose than previously reported. These findings further indicate that LVEF is not an accurate predictor of CHF in patients who receive doxorubicin.
Copyright 2003 American Cancer Society.
Similar articles
-
Subclinical late cardiomyopathy after doxorubicin therapy for lymphoma in adults.J Clin Oncol. 2004 May 15;22(10):1864-71. doi: 10.1200/JCO.2004.06.033. J Clin Oncol. 2004. PMID: 15143078
-
Role of hypertension on new onset congestive heart failure in patients receiving trastuzumab therapy for breast cancer.J Cardiovasc Med (Hagerstown). 2014 Feb;15(2):141-6. doi: 10.2459/JCM.0b013e328365afb5. J Cardiovasc Med (Hagerstown). 2014. PMID: 24534802
-
[Changes in left ventricular function during chemotherapy with doxorubicin].Vnitr Lek. 1999 Jul;45(7):395-402. Vnitr Lek. 1999. PMID: 11045157 Czech.
-
Adriamycin (doxorubicin) cardiotoxicity: a review.West J Med. 1979 Nov;131(5):364-8. West J Med. 1979. PMID: 394479 Free PMC article. Review.
-
Radionuclide ventriculography for evaluation and prevention of doxorubicin cardiotoxicity.Clin Ther. 1985;7(6):660-7. Clin Ther. 1985. PMID: 3907840 Review.
Cited by
-
Premedication with pioglitazone prevents doxorubicin-induced left ventricular dysfunction in mice.BMC Pharmacol Toxicol. 2021 May 7;22(1):27. doi: 10.1186/s40360-021-00495-w. BMC Pharmacol Toxicol. 2021. PMID: 33962676 Free PMC article.
-
Circulating Levels of Epirubicin Cause Endothelial Senescence While Compromising Metabolic Activity and Vascular Function.Front Cell Dev Biol. 2020 Aug 19;8:799. doi: 10.3389/fcell.2020.00799. eCollection 2020. Front Cell Dev Biol. 2020. PMID: 32974345 Free PMC article.
-
Late Cardiotoxicity: Issues for Childhood Cancer Survivors.Curr Treat Options Cardiovasc Med. 2016 Jul;18(7):47. doi: 10.1007/s11936-016-0466-6. Curr Treat Options Cardiovasc Med. 2016. PMID: 27230282 Review.
-
Transcriptome profiling of peripheral blood cells identifies potential biomarkers for doxorubicin cardiotoxicity in a rat model.PLoS One. 2012;7(11):e48398. doi: 10.1371/journal.pone.0048398. Epub 2012 Nov 27. PLoS One. 2012. PMID: 23209553 Free PMC article.
-
Weekly pegylated liposomal doxorubicin and paclitaxel in patients with metastatic breast carcinoma: A phase II study.Oncol Lett. 2010 Jul;1(4):749-753. doi: 10.3892/ol_00000131. Epub 2010 Jul 1. Oncol Lett. 2010. PMID: 22966374 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical