Bakowski M T, Prentice H G, Lister T A, Malpas J S, McElwain T J, Powles R L
Cancer Treat Rep. 1979 Jan;63(1):127-9.
Twenty-eight patients with advanced acute nonlymphocytic leukemia, 16 with acute lymphoblastic leukemia, and two with acute undifferentiated leukemia were treated with ICRF-159. No patient achieved a complete remission and only three patients (6%) achieved a partial bone marrow remission. The only significant toxic effect was myelosuppression which probably contributed to the death of six patients. Five patients with acute nonlymphocytic leukemia and one with acute lymphoblastic leukemia received a combination of ICRF-159 and low-dose cytosine arabinoside. There were no remissions in this group and the toxic effects were more marked than with ICRF-159 alone. This study confirms the limited activity of ICRF-159 as a single agent in acute leukemia demonstrated in smaller series, and shows that, when used in combination with low-dose cytosine arabinoside, it was ineffective and resulted in increased toxicity. ICRF-159 alone or in combination with cytosine arabinoside has very limited activity in advanced adult acute leukemia.
28例晚期急性非淋巴细胞白血病患者、16例急性淋巴细胞白血病患者和2例急性未分化白血病患者接受了ICRF - 159治疗。无患者达到完全缓解,仅3例患者(6%)达到部分骨髓缓解。唯一显著的毒性作用是骨髓抑制,这可能导致了6例患者死亡。5例急性非淋巴细胞白血病患者和1例急性淋巴细胞白血病患者接受了ICRF - 159与小剂量阿糖胞苷的联合治疗。该组无缓解,且毒性作用比单独使用ICRF - 159时更明显。本研究证实了ICRF - 159作为单一药物在急性白血病中的活性有限,这在较小系列研究中已得到证明,并且表明,当与小剂量阿糖胞苷联合使用时,它无效且导致毒性增加。单独使用ICRF - 159或与阿糖胞苷联合使用在晚期成人急性白血病中的活性非常有限。