Plasma concentrations of venetoclax and Pharmacogenetics correlated with drug efficacy in treatment naive leukemia patients: a retrospective study.

IF 2.9 3区 医学 Q2 GENETICS & HEREDITY Pharmacogenomics Journal Pub Date : 2024-11-22 DOI:10.1038/s41397-024-00359-6
Yue Li, Qing Wan, Jiaqi Wan, Xiong Xiao, Jinfang Hu, Xintong Yang, Fancong Kong, Jieyu Wang, Baoquan Song, Zhentao Li, Fei Li, Simei Ren, Hongwei Peng
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Abstract

Venetoclax (VEN) was the only Bcl-2 inhibitor approved yet and showed large differences in clinical efficacy. The aim of the study was to explore the relationships between the plasma concentration and efficacy of VEN, and identify potential influencing factors. A retrospective cohort study was conducted and a total of 76 trough (C0h) and 91 6 h post-dose plasma concentration (C6h) blood concentrations of VEN were collected in 54 patients. C6h/D concentration of VEN was found to be significantly correlated with treatment efficacy (p = 0.006) in leukemia patients with good or intermediate prognosis stratification. A ROC curve was then established and the cut-off value was calculated as 0.2868 μg/ml (AUC = 0.7097, p = 0.1081). Besides, patients co-administered with triazoles or carrying CYP3A5 rs776746 AA/AG genotypes were prone to induce higher VEN plasma concentration regardless of whether VEN dosage was reduced or not. Through LASSO-logistic regression and nomogram analysis, chemotherapy regimens and neutrophil percentages were identified as the critical elements that may predict drug response. Above all, in addition to identify prognostic stratification, AML patients taken with VEN were suggested to test plasma concentration routinely so as to achieve desired efficacy, especially when co-administered with triazoles or carried with CYP3A5 rs776746 AA/AG.

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一项回顾性研究:Venetoclax 的血浆浓度和药物遗传学与治疗前白血病患者的疗效相关。
Venetoclax(VEN)是目前唯一获批的Bcl-2抑制剂,其临床疗效差异很大。该研究旨在探讨VEN的血浆浓度与疗效之间的关系,并找出潜在的影响因素。研究采用回顾性队列研究方法,共收集了54名患者的76份谷浓度(C0h)和91份给药后6小时血浆浓度(C6h)。研究发现,在预后分层为良好或中等的白血病患者中,VEN的C6h/D浓度与治疗效果明显相关(p = 0.006)。随后建立了 ROC 曲线,并计算出临界值为 0.2868 μg/ml(AUC = 0.7097,p = 0.1081)。此外,合用三唑类药物或携带 CYP3A5 rs776746 AA/AG 基因型的患者,无论是否减少 VEN 的剂量,均易诱发 VEN 血浆浓度升高。通过LASSO-逻辑回归和提名图分析,化疗方案和中性粒细胞百分比被确定为可能预测药物反应的关键因素。此外,除了确定预后分层外,还建议使用 VEN 的急性髓细胞白血病患者定期检测血浆浓度,以达到预期疗效,尤其是与三唑类药物合用或携带 CYP3A5 rs776746 AA/AG 时。
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来源期刊
Pharmacogenomics Journal
Pharmacogenomics Journal 医学-药学
CiteScore
7.20
自引率
0.00%
发文量
35
审稿时长
6-12 weeks
期刊介绍: The Pharmacogenomics Journal is a print and electronic journal, which is dedicated to the rapid publication of original research on pharmacogenomics and its clinical applications. Key areas of coverage include: Personalized medicine Effects of genetic variability on drug toxicity and efficacy Identification and functional characterization of polymorphisms relevant to drug action Pharmacodynamic and pharmacokinetic variations and drug efficacy Integration of new developments in the genome project and proteomics into clinical medicine, pharmacology, and therapeutics Clinical applications of genomic science Identification of novel genomic targets for drug development Potential benefits of pharmacogenomics.
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