Wang Y F, Curtis J E, Lipton J, Minkin S, McCulloch E A
Ontario Cancer Institute, University of Toronto, Ontario, Canada.
Leukemia. 1991 Jun;5(6):522-7.
Cytosine arabinoside (ara-C) and cis-dichlorodiammineplatinum II (cisplatin) are lethal to mammalian cells by very different mechanisms; however, they share interactions with the biology of blast cells in acute myelogeneous leukemia (AML). Both agents are more toxic to AML blasts in suspension than when a clonogenic assay in methyl cellulose is used; both agents are more toxic in suspension in the presence of rG-CSF than with rGM-CSF. Accordingly, preclinical tests were undertaken of cisplatin and ara-C in combination. At the same time, a phase I/II clinical trial of the combination was conducted, using AML patients refractory to treatment or in relapse. In the laboratory, blasts from eight AML patients were tested against each agent singly and in combination. The observed survival values for the mixture were compared with those predicted by assuming either an additive effect or a more general effect that allows synergism or antagonism. Blasts from two patients were tested with this design in the presence of rG-CSF or rGM-CSF. In most instances the toxic effects of ara-C and cisplatin were additive. Evidence of synergism was seen in blasts from three patients.
阿糖胞苷(ara-C)和顺二氯二氨铂(II)(顺铂)通过截然不同的机制对哺乳动物细胞具有致死性;然而,它们在急性髓性白血病(AML)中与原始细胞生物学存在共同的相互作用。这两种药物对悬浮状态的AML原始细胞的毒性均高于在甲基纤维素中进行克隆形成试验时的毒性;在重组人粒细胞集落刺激因子(rG-CSF)存在的情况下,这两种药物在悬浮状态下的毒性均高于在重组人粒细胞巨噬细胞集落刺激因子(rGM-CSF)存在时的毒性。因此,开展了顺铂和阿糖胞苷联合用药的临床前试验。与此同时,针对难治性或复发的AML患者进行了该联合用药的I/II期临床试验。在实验室中,对8例AML患者的原始细胞分别进行了单一药物及联合用药测试。将混合物的观察到的存活值与通过假设为相加效应或允许协同或拮抗作用的更一般效应所预测的值进行比较。在rG-CSF或rGM-CSF存在的情况下,采用该设计对2例患者的原始细胞进行了测试。在大多数情况下,阿糖胞苷和顺铂的毒性作用是相加的。在3例患者的原始细胞中观察到了协同作用的证据。