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Mitoxantrone-induced cardiotoxicity in patients with multiple sclerosis
Ali Hamzehloo1, Masood Etemadifar
1Department of Neurology, Isfahan University of Medical Sciences, Isfahan, Iran. ali-hamzeloo@yahoo.com
Background:
There are few treatment options for patients with secondary progressive and worsening relapsing-remitting multiple sclerosis. Mitoxantrone is an antineoplastic drug, recently approved for treatment of multiple sclerosis. Mitoxantrone is, however, associated with dose-related cardiotoxicity, which limits its use.
Objective:
To investigate the possible cardiotoxicity of mitoxantrone in multiple sclerosis.
Methods:
We studied 96 patients with worsening relapsing-remitting or secondary progressive multiple sclerosis, to evaluate cardiotoxicity within one year of mitoxantrone therapy. This study was performed in the Multiple Sclerosis Clinic of Isfahan University of Medical Sciences from October 2003 through October 2004. Analysis of mitoxantrone therapy (12 mg/m2), in terms of cardiac toxicity, was conducted on patients who received at least 4 doses. Cardiac assessment was carried out every 6 months with electrocardiogram, as well as a spectral and color-flow Doppler echocardiographic examination at the time of enrollment and 6 and 12 months later.
Results:
Ninety-six patients were assessed over 12 months. There was no evidence of clinically-significant cardiac dysfunction. Three patients had a left ventricular ejection fraction of <10% of the base-line value and three had <50%.
Conclusion:
Mitoxantrone (12 mg/m2) is effective and generally well tolerated by patients with worsening relapsing-remitting and secondary progressive multiple sclerosis. Our findings suggest that the risk for developing cardiotoxicity is low in patients with multiple sclerosis within one year of the treatment with mitoxantrone.
Insights
Mitoxantrone is an effective treatment for multiple sclerosis, with a low risk of cardiotoxicity observed in patients over one year. This study indicates the drug is generally well-tolerated in those with progressive forms of the disease.
Area of Science:
- Neurology
- Cardiology
- Pharmacology
Background:
- Limited treatment options exist for secondary progressive and worsening relapsing-remitting multiple sclerosis (MS).
- Mitoxantrone, an antineoplastic agent, is approved for MS treatment but carries a risk of dose-related cardiotoxicity.
- This cardiotoxicity can restrict the clinical utility of mitoxantrone in managing MS.
Purpose of the Study:
- To investigate the potential cardiotoxicity associated with mitoxantrone therapy in multiple sclerosis patients.
- To evaluate cardiac function in MS patients undergoing mitoxantrone treatment over a one-year period.
Main Methods:
- A cohort of 96 patients with worsening relapsing-remitting or secondary progressive MS was studied.
- Cardiac assessments, including electrocardiogram and echocardiography, were performed at baseline and at 6 and 12 months.
- Patients received mitoxantrone at a dose of 12 mg/m², with analysis focused on those receiving at least 4 doses.
Main Results:
- No clinically significant cardiac dysfunction was observed in the 96 patients over 12 months.
- Three patients experienced a decrease in left ventricular ejection fraction (LVEF) of <10% from baseline.
- Three patients had an LVEF below 50%.
Conclusions:
- Mitoxantrone (12 mg/m²) is an effective and generally well-tolerated treatment for progressive MS.
- The risk of developing cardiotoxicity appears low in multiple sclerosis patients within one year of mitoxantrone therapy.
- Mitoxantrone can be considered a viable option for managing specific MS subtypes, with careful cardiac monitoring.
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