Clinical pharmacokinetics and drug-drug interactions of tyrosine-kinase inhibitors in chronic myeloid leukemia: A clinical perspective

被引:4
作者
Cheng, Fang [1 ,2 ]
Wang, Hongxiang [3 ]
Li, Weiming [4 ]
Zhang, Yu [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Pharm, Wuhan 430022, Peoples R China
[2] Hubei Prov Clin Res Ctr Precis Med Crit Illness, Wuhan 430022, Peoples R China
[3] Cent Hosp Wuhan, Dept Hematol, Wuhan 430014, Peoples R China
[4] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Hematol, Wuhan 430022, Peoples R China
关键词
Tyrosine kinase inhibitors; Clinical pharmacokinetics; Drug-drug interactions; Chronic myeloid leukemia; Drug metabolism; CHRONIC HEPATIC IMPAIRMENT; ST-JOHNS-WORT; IMATINIB MESYLATE; P-GLYCOPROTEIN; PRECLINICAL PHARMACOKINETICS; PHILADELPHIA-CHROMOSOME; MULTIDRUG-RESISTANCE; CYTOCHROME-P450; 3A4; BRAIN ACCUMULATION; MAIN METABOLITE;
D O I
10.1016/j.critrevonc.2024.104258
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the past decade, numerous tyrosine kinase inhibitors (TKIs) have been introduced in the treatment of chronic myeloid leukemia. Given the significant interpatient variability in TKIs pharmacokinetics, potential drug-drug interactions (DDIs) can greatly impact patient therapy. This review aims to discuss the pharmacokinetic characteristics of TKIs, specifically focusing on their absorption, distribution, metabolism, and excretion profiles. Additionally, it provides a comprehensive overview of the utilization of TKIs in special populations such as the elderly, children, and patients with liver or kidney dysfunction. We also highlight known or suspected DDIs between TKIs and other drugs, highlighting various clinically relevant interactions. Moreover, specific recommendations are provided to guide haemato-oncologists, oncologists, and clinical pharmacists in managing DDIs during TKI treatment in daily clinical practice.
引用
收藏
页数:14
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