米托坦
加药
药代动力学
生物利用度
药物遗传学
医学
肾上腺皮质癌
药理学
肿瘤科
个性化医疗
血浆浓度
内科学
生物信息学
化学
生物
生物化学
基因型
基因
作者
Rebecca V. Steenaard,Madeleine H. T. Ettaieb,Thomas Kerkhofs,Harm R. Haak
标识
DOI:10.1080/17425255.2021.1921146
摘要
Mitotane is the only drug registered specifically for adrenocortical carcinoma. Finding the optimal dose for a patient is difficult due to large differences in bioavailability, toxicity and effect. We therefore look to improve personalized dosing of mitotane.We searched PubMed for studies related to mitotane dosing, pharmacokinetics, pharmacogenetics and combination therapy. Comparison of different dosing strategies have not resulted in an optimal advice. Several computerized pharmacokinetic models have been proposed to predict plasma levels. The current pharmacokinetic models do not explain the full variance in plasma levels. Pharmacogenetics have been proposed to find the unexplained variance. Studies on combination therapy have not yet led to a potential dose adjustment for mitotane.Computerized pharmacokinetics models are promising tools to predict plasma levels, further validation is needed. Pharmacogenetics are introduced in these models, but more research is required before clinical application. We believe that in the near future, personalized mitotane dosage will be aided by a validated web-based pharmacokinetic model with good predictive ability based primarily on clinical characteristics, adjustable for actual plasma levels and dosage.
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