Sezaki T, Adachi T, Ishii H, Asano K, Takahashi I, Kimura I
Jpn J Clin Oncol. 1984 Sep;14(3):353-8.
Fourteen patients with multiple myeloma received aclarubicin (ACR) intravenous drip infusion at a dose of 15-25 mg/m2/day for 7 days every 3 weeks. Nine of the patients achieved more than a 25% reduction in M-protein. In two of the nine the reduction was more than 50% and the duration of their responses was 2.0 and 2.8 months, respectively. In the nine cases of previous combination chemotherapy-resistant multiple myeloma, five showed more than a 25% reduction and one of them showed more than a 50% reduction in M-protein. One of the two patients with tumors achieved a marked regression of the tumor mass and two of the 14 patients showed marked improvement in subjective symptoms. Hematological toxicity, anorexia, nausea and vomiting occurred frequently. However, no cardiac toxicity obviously attributable to ACR was detected, and alopecia was generally mild. Thus, the above results indicate that ACR may be useful in combination chemotherapy for multiple myeloma because of its effectiveness and relatively low dose-limiting factors.
14例多发性骨髓瘤患者接受阿柔比星(ACR)静脉滴注,剂量为15 - 25mg/m²/天,每3周连续给药7天。其中9例患者的M蛋白降低超过25%。在这9例患者中有2例降低超过50%,其缓解持续时间分别为2.0个月和2.8个月。在之前接受联合化疗耐药的9例多发性骨髓瘤患者中,5例M蛋白降低超过25%,其中1例降低超过50%。2例肿瘤患者中有1例肿瘤肿块明显消退,14例患者中有2例主观症状明显改善。血液学毒性、厌食、恶心和呕吐频繁发生。然而,未检测到明显归因于ACR的心脏毒性,脱发一般较轻。因此,上述结果表明,由于ACR的有效性和相对较低的剂量限制因素,其可能在多发性骨髓瘤的联合化疗中有用。