药物管理的替代途径:暴露伊马替尼使用不同的配方。

IF 2.7 4区 医学 Q3 ONCOLOGY
H B Fiebrich-Westra, O Visser, A B Francken, E J Smolders
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引用次数: 0

摘要

目的:探讨伊马替尼替代制剂治疗患者的可能性。方法:对2例患者采用不同的肠内直肠伊马替尼制剂进行治疗。在治疗期间,测量血浆浓度以确保充分暴露。结果:1例患者经十二指肠管给予伊马替尼混悬液。使用400 mg BID时,患者的伊马替尼血药浓度为750µg/L。将剂量增加到BID 600 mg后,伊马替尼血药浓度为1500µg/L (GIST治疗目标浓度为1100µg/L)。直肠给药没有导致足够的血浆浓度。第二组在口服混悬液和通过试管服用时都有足够的伊马替尼暴露(目标CML治疗为1000 μ g/L)。结论:对于能够吞咽液体的患者,我们更倾向于使用悬浮剂伊马替尼片(与药品说明书相当)。如果患者有十二指肠管,则可选择使用含有粉状片剂的悬浮液基座。基于病例1中发现的极低暴露,我们不建议直肠给药。我们建议使用标签外给药形式时监测血浆浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alternative routes of drug administration: exposure of imatinib using different formulations.

Purpose: To explore the possibility of treating patients with alternative imatinib formulations.

Methods: Two patients were treated with different enteral en rectal imatinib formulations. During treatment plasma concentrations where measured to assure adequate exposure.

Results: The first patient received imatinib suspension through the duodenum tube. With a dose of 400 mg BID the patient had an imatinib plasma concentration of 750 µg/L. After increasing the dose to 600 mg BID the imatinib plasma concentration was 1500 µg/L (target GIST treatment > 1100 µg/L). Rectal administration of the tablet did not lead to sufficient plasma concentrations. The second had adequate exposure of imatinib both when the suspension was taken orally and through the tube (target CML treatment are > 1000 µg/L).

Conclusion: For patients able to swallow liquids, we prefer the suspended imatinib tablets (comparable to drug label). If patients have a duodenum tube the use of a suspension base with pulverized tablets could be an alternative. Based on the extremely low exposure found in case 1, we do not recommend rectal administration of tablets. We recommend the monitor plasma concentrations when off label dosing forms are used.

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来源期刊
CiteScore
6.10
自引率
3.30%
发文量
116
审稿时长
2.5 months
期刊介绍: Addressing a wide range of pharmacologic and oncologic concerns on both experimental and clinical levels, Cancer Chemotherapy and Pharmacology is an eminent journal in the field. The primary focus in this rapid publication medium is on new anticancer agents, their experimental screening, preclinical toxicology and pharmacology, single and combined drug administration modalities, and clinical phase I, II and III trials. It is essential reading for pharmacologists and oncologists giving results recorded in the following areas: clinical toxicology, pharmacokinetics, pharmacodynamics, drug interactions, and indications for chemotherapy in cancer treatment strategy.
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