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A novel 6-mercaptopurine oral liquid formulation for pediatric acute lymphoblastic leukemia patients - Results of a randomized clinical trial

机译:小儿急性淋巴细胞白血病患者的新型6-巯基嘌呤口服液制剂-一项随机临床试验的结果

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Objective: Pediatric patients with acute lymphoblastic leukemia (ALL) are treated with oral 6-mercaptopurine (6MP) for nearly 2 years, but no pediatric formulation has been available. In this study, an oral 6MP liquid suitable for pediatric use was developed and tested in the target population. Method: A randomized cross-over study was performed in 20 pediatric ALL patients (age 1.9 - 14.6 years), comparing pharmacokinetics and pharmacodynamics of a newly developed 6MP liquid formulation to 6MP capsules, both taken orally for 4 weeks. Results: Based upon trough levels of the principal active metabolite, 6-thioguanine nucleotides (6-TGN), a relative bioavailability of the liquid vs. capsules of 1.01 was found (90% CI 0.86 - 1.20), demonstrating bioequivalence. This was supported by the similarly observed 6MP dosages needed for leucocyte depletion, for both formulations (35 mg/day (range 10 - 115 mg)). 75% of the parents/patients (p = 0.005) preferred the oral liquid over the capsules because of the ease of administration. Conclusion: We conclude that the novel 6MP liquid is a promising treatment for ALL.
机译:目的:小儿急性淋巴细胞白血病(ALL)患者接受口服6-巯基嘌呤(6MP)治疗近两年,但尚无小儿用药。在这项研究中,开发了适合儿童使用的口服6MP液体,并在目标人群中进行了测试。方法:对20名小儿ALL患者(年龄1.9-14.6岁)进行了一项随机交叉研究,比较了新开发的6MP液体制剂与6MP胶囊的药代动力学和药效学,均口服4周。结果:基于主要活性代谢物6-硫鸟嘌呤核苷酸(6-TGN)的谷值,发现液体与胶囊的相对生物利用度为1.01(90%CI 0.86-1.20),证明了生物等效性。对于两种制剂,白细胞耗竭所需的相似观察到的6MP剂量(35 mg /天(10-115 mg))支持了这一点。 75%的父母/患者(p = 0.005)由于易于服用,因此比口服胶囊更喜欢口服液。结论:我们得出结论,新型6MP液体是ALL的有希望的治疗方法。

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