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

威尼斯人 药物遗传学 肿瘤科 医学 药品 药理学 回顾性队列研究 内科学 白血病 生物 遗传学 基因型 基因 慢性淋巴细胞白血病
作者
Hongwei Peng,Yue Li,Qing Wan,Jinfang Hu,Xiong Xiao,Xintong Yang,Fancong Kong,Jieyu Wang,Baoquan Song,Zhentao Li,Simei Ren
出处
期刊:Research Square - Research Square
标识
DOI:10.21203/rs.3.rs-4565192/v1
摘要

Abstract Introduction: Venetoclax (VEN) was the only Bcl-2 inhibitor approved by FDA and showed desired efficacy. However, VEN showed large differences in clinical efficacy, which may due to pharmacokinetic variability. Objectives:The purpose of the study was to explore the relationships between the plasma concentration and efficacy of VEN, and identify potential influencing factors. Methods: A retrospective cohort study was conducted in the First Affiliated Hospital of Nanchang University from March 2022 to March 2024. LC-MS/MS was used to monitor the concentration of VEN. Pharmacogenetics was determined by DNA sequence. Results: A total of 76 trough (C0h) and 91 6h post-dose plasma concentration (C6h) blood concentrations of VEN were collected in 54 patients. C6h/D concentration of VEN was significantly correlated with treatment efficacy (P = 0.006) in Leukemia patients with good or intermediate prognosis. A ROC curve was then established and the cut-off value was calculated as 0.2868 µg/ml.kg.mg-1(AUC = 0.7097, P = 0.1081). Furthermore, the research uncovered correlations among the co-administration of triazoles, CYP3A5 rs776746 and ABCB1 genotypes with VEN plasma concentrations. Through LASSO-logistic regression and nomagram analysis, ELN prognostic stratification and neutrophil percentages were determined as the critical elements that may predict drug response. Conclusions: Our results confirmed that ELN stratification was applicable in predicting drug response in treatment native unfit AML patients. C6h/D level may correlate with drug response especially in good and moderate stratification patients. Patients co-administered with triazoles or carried with AA/AG CYP3A5 rs776746 should be paid more attention in order to attain sustainable efficacy with limited toxicity.
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