Stewart D J, Perrault D J, Maroun J A, Lefebvre B M
Am J Clin Oncol. 1987 Aug;10(4):335-40. doi: 10.1097/00000421-198708000-00016.
Twenty-three patients with advanced breast cancer were treated with the combination of mitoxantrone and doxorubicin. This study was conducted since there is incomplete cross-resistance between the two drugs, and since data in vitro suggested that mitoxantrone might decrease the cardiotoxicity of concurrently administered doxorubicin by decreasing doxorubicin-induced membrane lipid peroxidation. Of 20 patients who were evaluable for response, 10 (50%) responded. Myelosuppression was pronounced with mitoxantrone doses ranging from 6 to 10 mg/m2 and doxorubicin doses ranging from 30 to 50 mg/m2, but granulocytopenia-related infections were uncommon. Three of 14 patients who had repeated gated cardiac radionuclide scans had reductions in their ejection fractions of 26% or more at relatively small total cumulative doses of the drugs; one patient developed reversible congestive heart failure after having received high cumulative doses of the two drugs. Preliminary clinical data suggest that mitoxantrone does not protect patients from doxorubicin-induced cardiotoxicity. Other toxicity was generally mild.
23例晚期乳腺癌患者接受了米托蒽醌和阿霉素联合治疗。开展这项研究是因为这两种药物之间存在不完全交叉耐药性,且体外数据表明米托蒽醌可能通过减少阿霉素诱导的膜脂质过氧化来降低同时使用的阿霉素的心脏毒性。在可评估疗效的20例患者中,10例(50%)有反应。当米托蒽醌剂量为6至10mg/m²、阿霉素剂量为30至50mg/m²时,骨髓抑制明显,但粒细胞减少相关感染并不常见。14例接受重复门控心脏放射性核素扫描的患者中,有3例在相对较小的药物总累积剂量下射血分数降低了26%或更多;1例患者在接受高累积剂量的两种药物后出现可逆性充血性心力衰竭。初步临床数据表明,米托蒽醌不能保护患者免受阿霉素诱导的心脏毒性。其他毒性一般较轻。