Carmo-Pereira J, Costa F O, Henriques E, Cantinho-Lopes M G, Godinho F, Sales-Luis A
Instituto Portugues de Oncologia Francisco Gentil, Lisboa.
Eur J Cancer Clin Oncol. 1988 Mar;24(3):473-6. doi: 10.1016/s0277-5379(98)90019-0.
Thirty-seven evaluable patients with progressive disseminated breast carcinoma were treated with a combination of mitoxantrone 14 mg/m2 i.v. every 3 weeks plus prednisone 20 mg/m2 p.o. daily with a reducing dose over several weeks. Thirteen of 37 patients (35%) achieved an objective response with two complete regressions. The median duration of response was 7 months and the median duration of survival 14 months. The cardiac function of all patients was monitored by serial left ventricular ejection fraction, at rest and after stress, and 3-monthly thereafter. Ten patients showed a deterioration in the ejection fraction after a minimum cumulative dose of 86 mg/m2 (six cycles), but only four developed clinical cardiac failure which was easily reversible after stopping mitoxantrone. Leucopenia was the dose-limiting toxicity. Nausea and/or vomiting were generally mild and transient. Alopecia was minimal. These results confirmed that this combination is effective and well tolerated in the treatment of disseminated breast carcinoma, and cardiotoxicity can be avoided with adequate monitoring of the left ventricular ejection fraction after six cycles of therapy (86 mg/m2).
37例可评估的进展性播散性乳腺癌患者接受了米托蒽醌14mg/m²静脉注射,每3周1次,联合泼尼松20mg/m²口服,每日1次,并在数周内逐渐减量的治疗。37例患者中有13例(35%)获得客观缓解,其中2例完全缓解。缓解的中位持续时间为7个月,中位生存期为14个月。所有患者的心脏功能通过连续监测静息和应激状态下的左心室射血分数进行监测,此后每3个月监测1次。10例患者在累积最小剂量达86mg/m²(六个周期)后出现射血分数恶化,但只有4例发生临床心力衰竭,停用米托蒽醌后心力衰竭易于逆转。白细胞减少是剂量限制性毒性。恶心和/或呕吐一般较轻且为一过性。脱发极少。这些结果证实,该联合方案在治疗播散性乳腺癌方面有效且耐受性良好,并且在六个周期治疗(86mg/m²)后通过充分监测左心室射血分数可避免心脏毒性。