Schütte J, Niederle N, Seeber S
J Cancer Res Clin Oncol. 1983;105(2):162-5. doi: 10.1007/BF00406927.
Aclacinomycin A (ACM) is a new anthracycline antibiotic with a reduced cardiac toxicity in animal models. A phase II study was performed in a total of 25 patients, 23 of whom are evaluable for response. All suffered from recurrent and advanced tumors. Pretreatment consisted of at least four different chemotherapeutic agents (range: 4-9). Lung cancer patients (3/9) were irradiated to the mediastinum. Eighteen patients were pretreated with doxo- or daunomycin. The dose for solid tumors was 2-3 mg/kg given on 3 consecutive days every 3 weeks. Leukemia patients received a daily dose of 20 mg/m2, and standard response criteria were used. Marked reductions of leukocyte counts were achieved in leukemia patients. The overall response rate was about 15% in solid tumors, but major objective responses (CR + PR) have not been observed. Myelosuppression was commonly moderate in solid tumor patients, nausea and vomiting were rare, and alopecia was not induced. Cumulative cardiotoxicity was not evaluated in this trial. Treatment with ACM requires further investigation in acute leukemias and solid tumors, not pretreated with anthracycline antibiotics.
阿克拉霉素A(ACM)是一种新型蒽环类抗生素,在动物模型中具有较低的心脏毒性。对总共25例患者进行了II期研究,其中23例可评估疗效。所有患者均患有复发性和晚期肿瘤。预处理包括至少四种不同的化疗药物(范围:4 - 9种)。肺癌患者(3/9)接受了纵隔照射。18例患者接受过阿霉素或柔红霉素预处理。实体瘤患者的剂量为每3周连续3天给予2 - 3 mg/kg。白血病患者的日剂量为20 mg/m²,并采用标准的疗效标准。白血病患者的白细胞计数显著降低。实体瘤的总体缓解率约为15%,但未观察到主要客观缓解(CR + PR)。实体瘤患者的骨髓抑制通常为中度,恶心和呕吐少见,且未诱导脱发。本试验未评估累积心脏毒性。对于未用蒽环类抗生素预处理的急性白血病和实体瘤患者,ACM治疗需要进一步研究。