Suppression of mitoxantrone cardiotoxicity in multiple sclerosis patients by dexrazoxane

Ann Neurol. 2006 Jan;59(1):206-9. doi: 10.1002/ana.20747.

Abstract

Objective: To explore the potential of dexrazoxane to suppress subclinical cardiotoxicity in MS patients receiving mitoxantrone.

Methods: An open-label study was performed to evaluate possible subclinical cardiotoxicity in multiple sclerosis patients treated quarterly with mitoxantrone (48 mg/m(2) cumulative), with and without concomitant dexrazoxane, using blinded serial radionucleide ventriculography.

Results: No patient experienced symptoms of heart failure. Patients receiving dexrazoxane, which is cardioprotective for anthracyclines, exhibited a significantly lesser decline in left ventricular ejection fraction (mean change, -3.80% vs -8.55%, p < 0.001).

Interpretation: These results support a cardioprotective effect of dexrazoxane in mitoxantrone treated multiple sclerosis patients.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Antineoplastic Agents* / therapeutic use
  • Antineoplastic Agents* / toxicity
  • Cardiovascular Agents / metabolism
  • Cardiovascular Agents / therapeutic use
  • Female
  • Heart Failure / chemically induced*
  • Humans
  • Male
  • Middle Aged
  • Mitoxantrone* / therapeutic use
  • Mitoxantrone* / toxicity
  • Multiple Sclerosis / drug therapy*
  • Razoxane / metabolism
  • Razoxane / therapeutic use
  • Stroke Volume
  • Troponin I / metabolism

Substances

  • Antineoplastic Agents
  • Cardiovascular Agents
  • Troponin I
  • Razoxane
  • Mitoxantrone