Lennard L, Rees C A, Lilleyman J S, Maddocks J L
Br J Clin Pharmacol. 1983 Oct;16(4):359-63. doi: 10.1111/j.1365-2125.1983.tb02178.x.
6-Mercaptopurine is extensively used in the treatment of childhood lymphoblastic leukaemia to prolong the duration of remission achieved with other drugs. The response to remission maintenance therapy varies widely. We investigated the relationship between red blood cell 6-thioguanine nucleotide, a metabolite of 6-mercaptopurine, and myelosuppression in 22 children with acute lymphoblastic leukaemia in remission. The peripheral neutrophil count was used as an index of myelosuppression. 6-Mercaptopurine dose was related to 6-thioguanine nucleotide concentration (r = 0.4; P less than 0.001; n = 90; y = 18.51 + 0.36 x). Large individual variations around the regression line are observed. Neither 6-mercaptopurine dose nor 6-thioguanine nucleotide concentration was related to the neutrophil count at the time of sampling (day 0) or 7 days later. Both 6-mercaptopurine dose and 6-thioguanine nucleotide concentration correlated with the neutrophil count at day 14 (r = -0.33; P less than 0.01; n = 90 and r = -0.3; P less than 0.01; n = 90 respectively). This delay is compatible with a cytotoxic action on bone marrow stem cells. Excluding children with other, uncontrolled, potentially myelosuppressive influences the correlation between 6-thioguanine nucleotide concentration and neutropenia improved (r = -0.6; P less than 0.001; n = 37). A significant degree of neutropenia was observed by day 14 if the 6-thioguanine nucleotide concentration (day 0) was greater than 210 pmol/8 X 10(8) RBCs. The assay of 6-thioguanine nucleotide may highlight those individuals with pharmacokinetic resistance. Two children on continuous high dose 6-mercaptopurine, had low red blood cell 6-thioguanine nucleotide concentrations and neutropenia was not observed.
6-巯基嘌呤被广泛用于治疗儿童淋巴细胞白血病,以延长使用其他药物所达到的缓解期。缓解维持治疗的反应差异很大。我们调查了22例急性淋巴细胞白血病缓解期儿童红细胞6-硫鸟嘌呤核苷酸(6-巯基嘌呤的一种代谢产物)与骨髓抑制之间的关系。外周血中性粒细胞计数用作骨髓抑制的指标。6-巯基嘌呤剂量与6-硫鸟嘌呤核苷酸浓度相关(r = 0.4;P小于0.001;n = 90;y = 18.51 + 0.36x)。观察到回归线周围存在较大的个体差异。6-巯基嘌呤剂量和6-硫鸟嘌呤核苷酸浓度均与采样时(第0天)或7天后的中性粒细胞计数无关。6-巯基嘌呤剂量和6-硫鸟嘌呤核苷酸浓度均与第14天的中性粒细胞计数相关(r分别为-0.33;P小于0.01;n = 90和r = -0.3;P小于0.01;n = 90)。这种延迟与对骨髓干细胞的细胞毒性作用相符。排除受其他未控制的潜在骨髓抑制影响的儿童后,6-硫鸟嘌呤核苷酸浓度与中性粒细胞减少之间的相关性有所改善(r = -0.6;P小于0.oo丨;n = 37)。如果6-硫鸟嘌呤核苷酸浓度(第0天)大于210 pmol/8×10⁸红细胞,则在第14天观察到明显程度的中性粒细胞减少。6-硫鸟嘌呤核苷酸检测可能会凸显那些具有药代动力学抗性的个体。两名持续接受高剂量6-巯基嘌呤治疗的儿童,其红细胞6-硫鸟嘌呤核苷酸浓度较低,未观察到中性粒细胞减少。