Goffette Sophie, van Pesch Vincent, Vanoverschelde Jean Louis, Morandini Emmanuel, Sindic Christian J M
Service de Neurologie, Cliniques Universitaires Saint Luc, Université catholique de Louvain, Brussels, Belgium.
J Neurol. 2005 Oct;252(10):1217-22. doi: 10.1007/s00415-005-0839-3. Epub 2005 Apr 18.
Mitoxantrone is an approved drug for patients with worsening relapsing-remitting, secondary progressive and progressive relapsing multiple sclerosis (MS). From a cohort of 820 MS patients, 52 (6%) were treated with this drug between December 1991 and April 2003. Mitoxantrone was administered at a dose of 12 mg/m(2) once a month for three months and then at three-month intervals to reach a total cumulative dose of 144 mg/m(2). The left ventricular ejection fraction was checked by radionuclide ventriculography prior to treatment and every six months. Treatment was stopped if the ejection fraction was below 50% in two consecutive ventriculographies performed one to three months apart. Cardiotoxicity during the course of the treatment was not observed. However, three patients developed congestive heart failure 24, 39 and 80 months after the last dose of mitoxantrone. Other cardiac causes were excluded. Two of these patients had been treated previously with cyclophosphamide. All patients first recovered on medical treatment, but two worsened a few months later. One patient remained severely symptomatic in spite of optimal medical treatment. Although mitoxantrone is generally well tolerated and reduces progression of disability and clinical exacerbations, our observation of a delayed cardiotoxicity makes necessary a long-term follow-up of MS patients treated with this drug.
米托蒽醌是一种已获批用于治疗复发缓解型、继发进展型和进展复发型多发性硬化症(MS)病情恶化患者的药物。在1991年12月至2003年4月期间,从820名MS患者队列中,有52名(6%)接受了该药物治疗。米托蒽醌的给药剂量为12 mg/m²,每月一次,共三个月,然后每三个月给药一次,直至累积总剂量达到144 mg/m²。在治疗前及每六个月通过放射性核素心室造影检查左心室射血分数。如果在间隔一至三个月进行的两次连续心室造影中射血分数低于50%,则停止治疗。在治疗过程中未观察到心脏毒性。然而,三名患者在最后一剂米托蒽醌给药后24、39和80个月出现充血性心力衰竭。排除了其他心脏病因。其中两名患者此前曾接受环磷酰胺治疗。所有患者最初经药物治疗后病情好转,但有两名患者在几个月后病情恶化。尽管接受了最佳药物治疗,仍有一名患者症状严重。虽然米托蒽醌通常耐受性良好,可减少残疾进展和临床病情加重,但我们观察到的迟发性心脏毒性使得有必要对接受该药物治疗的MS患者进行长期随访。