Boldt D H, Von Hoff D D, Kuhn J G, Hersh M
Cancer Res. 1984 Oct;44(10):4661-6.
9-beta-D-Arabinofuranosyl-2-fluoroadenine-5'-monophosphate (NSC 312887) (2-F-ara-AMP) is a new purine antimetabolite with documented preclinical activity against a number of animal tumors. Data from in vitro studies and preclinical animal toxicology trials indicated that 2-F-ara-AMP might be lymphocytotoxic. We studied effects of 2-F-ara-AMP on peripheral lymphocytes of patients receiving the agent in a Phase I clinical trial. Eleven patients received 13 courses given by i.v. bolus daily for 5 days. Mononuclear cells were isolated, and lymphocyte subsets were quantitated by immunofluorescence and flow cytometry 1 day before treatment and 4 hr after the final infusion. Lymphocytopenia developed rapidly (median time to nadir, 6 days) and was reversible. Standard leukocyte counts, differential counts, and percentages of isolated mononuclear cells reactive with monoclonal antibodies were used to calculate numbers of peripheral cells in each major lymphocyte subpopulation. Total T-lymphocyte counts fell during all treatment courses, with calculated mean absolute T-cell counts decreasing by 90%. Decreases were observed in all major T-lymphocyte subsets. By contrast, calculated B-lymphocyte counts decreased an average of 50% and were noted to increase during two treatment cycles. We also compared in vitro recoveries of cells from each major lymphocyte subpopulation before and after administration of 2-F-ara-AMP. Recoveries of total mononuclear cells, total T-cells, and non-T-, non-B-cells all were reduced substantially by 2-F-ara-AMP, but B-cell recovery was not reduced. These in vivo data, the first in human subjects, are in agreement with in vitro studies of halopurine nucleotide analogues which have demonstrated that T-cells are more sensitive than are B-cells to the cytotoxic effects of these compounds.
9-β-D-阿拉伯呋喃糖基-2-氟腺嘌呤-5'-单磷酸(NSC 312887)(2-F-ara-AMP)是一种新型嘌呤抗代谢物,已证明其在临床前对多种动物肿瘤具有活性。体外研究和临床前动物毒理学试验的数据表明,2-F-ara-AMP可能具有淋巴细胞毒性。我们在一项I期临床试验中研究了2-F-ara-AMP对接受该药物治疗的患者外周淋巴细胞的影响。11名患者接受了13个疗程的治疗,通过静脉推注,每天1次,共5天。在治疗前1天和最后一次输注后4小时,分离单核细胞,并通过免疫荧光和流式细胞术对淋巴细胞亚群进行定量分析。淋巴细胞减少迅速出现(降至最低点的中位时间为6天)且是可逆的。使用标准白细胞计数、分类计数以及与单克隆抗体反应的分离单核细胞百分比来计算每个主要淋巴细胞亚群中的外周细胞数量。在所有治疗疗程中,总T淋巴细胞计数均下降,计算得出的平均绝对T细胞计数减少了90%。在所有主要T淋巴细胞亚群中均观察到减少。相比之下,计算得出的B淋巴细胞计数平均下降了50%,并在两个治疗周期中出现增加。我们还比较了2-F-ara-AMP给药前后各主要淋巴细胞亚群细胞的体外恢复情况。2-F-ara-AMP使总单核细胞、总T细胞以及非T、非B细胞的恢复均大幅降低,但B细胞的恢复未受影响。这些在人类受试者中的体内数据是首次报道,与对卤嘌呤核苷酸类似物的体外研究结果一致,这些研究表明T细胞比B细胞对这些化合物的细胞毒性作用更敏感。