Therapeutic Drug Monitoring of Protein Kinase Inhibitors in the Treatment of Non-small Cell Lung Cancer.

Q4 Biochemistry, Genetics and Molecular Biology
Judita Staša, Jana Gregorová, Ondřej Slanař, Martin Šíma
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引用次数: 0

Abstract

Targeted therapy with protein kinase inhibitors (PKIs) represents one of the important treatment options for non-small cell lung cancer (NSCLC). It has contributed to improve patients' survival and quality of life significantly. These anticancer drugs are administrated orally in flat-fixed doses despite the well-known large interpatient pharmacokinetic variability and the possible need for dose individualization. To optimize and individualize dosing of PKIs, and thereby increasing the effectiveness and safety of the treatment, therapeutic drug monitoring (TDM) is the most frequently mentioned method. Unlike other areas of medicine, TDM has been rather exceptional in oncological practise since there is a little evidence or no data for concentration-effect relationships of PKIs. Therefore, the aim of this review is to summarize the pharmacokinetic characteristics of PKIs and provide the evidence supporting the use of TDM for personalised treatment of patients with NSCLC.

蛋白激酶抑制剂治疗非小细胞肺癌癌症的药物监测。
蛋白激酶抑制剂(PKIs)的靶向治疗是癌症(NSCLC)的重要治疗选择之一。它有助于显著提高患者的生存率和生活质量。这些抗癌药物是以固定剂量口服给药的,尽管众所周知,患者间的药代动力学变化很大,可能需要剂量个性化。为了优化和个性化PKIs的给药,从而提高治疗的有效性和安全性,治疗药物监测(TDM)是最常提到的方法。与其他医学领域不同,TDM在肿瘤学实践中相当特殊,因为很少有证据或没有数据表明PKIs的浓度-效应关系。因此,本综述的目的是总结PKIs的药代动力学特征,并提供支持TDM用于NSCLC患者个性化治疗的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Prague medical report
Prague medical report Medicine-Medicine (all)
CiteScore
1.10
自引率
0.00%
发文量
19
审稿时长
20 weeks
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