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Exposure-Response Analyses of the Effects of Venetoclax, a Selective BCL-2 Inhibitor, on B-Lymphocyte and Total Lymphocyte Counts in Women with Systemic Lupus Erythematosus

机译:venetoclax,一种选择性Bcl-2抑制剂,B淋巴细胞和全身淋巴细胞总淋巴细胞计数的曝光 - 反应分析及全身性红斑狼疮

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摘要

Background Venetoclax is a selective inhibitor of B-cell lymphoma-2, which plays a role in the development of various autoimmune diseases including systemic lupus erythematosus. The aim of these analyses was to quantify the exposure-response relationship for venetoclax effects on B-lymphocyte and total lymphocyte counts as pharmacodynamic markers of efficacy and safety, respectively, in women with systemic lupus erythematosus. The developed modeling framework was also used to evaluate venetoclax effects following cyclic, continuous, or induction/maintenance dosing paradigms as potential dosing alternatives in systemic lupus erythematosus. Methods Serial pharmacokinetic and lymphocyte count data from 73 women enrolled in a phase I study of venetoclax (single doses of 10-500 mg or two cycles of 30-600 mg or placebo once daily for 7 days followed by a 21-day washout) were analyzed using a sequential population pharmacokinetic/pharmacodynamic modeling approach. Simulations to evaluate changes in B-lymphocyte and total lymphocyte counts following different venetoclax dosing scenarios were conducted. Results Effect of venetoclax plasma exposures on B lymphocytes was described using an indirect linear response model and on total lymphocytes using a maximal response (E-max) with an effect site compartment. Baseline lymphocyte counts were significant covariates on the slope and half maximal inhibitory concentration parameter estimates for the respective models; with higher baseline counts associated with a greater reduction upon treatment with venetoclax. Model simulations showed that continuous dosing with lower doses of venetoclax (e.g., 150 mg daily) are predicted to achieve similar maximal effects on B-lymphocyte counts compared to cyclic dosing with higher doses (e.g., 400 mg 1 week on/3 weeks off); with better recovery of total lymphocyte counts during off-treatment weeks for the cyclic regimens. Conclusions Venetoclax treatment in women with systemic lupus erythematosus was associated with exposure-dependent reductions in B lymphocytes, and to a lesser extent, total lymphocyte counts. Results from this study support evaluation of B-cell lymphoma-2 inhibitors as potential therapies for the treatment of systemic lupus erythematosus. Clinicaltrials.gov NCT01686555.
机译:背景技术Venetoclax是B细胞淋巴瘤-2的选择性抑制剂,其在各种自身免疫疾病的发展中起着作用,包括Systemic Lupus红斑狼疮。这些分析的目的是量化对B淋巴细胞和总淋巴细胞总淋巴细胞作为药效学和安全性的药效记录的曝光 - 反应关系,分别是系统性狼疮红斑狼疮的妇女。开发的建模框架还用于评估循环,连续或诱导/维持剂量范式以下作为系统性红斑狼疮的潜在配料替代品后的威尼癌患者。方法串行药代动力学和淋巴细胞计数来自73名女性的血液研究,I阶段研究venetoclax(单剂量为10-500毫克或每日30-600mg或安慰剂7天,其次是21天的冲洗)是使用顺序种群药代动力学/药效学建模方法进行分析。进行了评价B淋巴细胞和总淋巴细胞数量的变化的仿真进行了不同的威尼替肽给药情景。结果使用间接线性响应模型和使用最大响应(E-MAX)的间接线性响应模型和总淋巴细胞对B淋巴细胞对B淋巴细胞曝光的影响。基线淋巴细胞计数对各个模型的斜坡和半最大抑制浓度参数估计有显着的协变量;在用嘌呤醛糖处理时,具有更高的基线计数与更大的减少相关。模拟模拟表明,与具有较高剂量的循环计量相比,预计具有较低剂量的尿蛋白(例如150mg日)的连续给药,以实现对B淋巴细胞计数的类似的最大效应(例如,截止/ 3周/ 3周400mg 1周) ;在循环方案的离处理周内更好地恢复总淋巴细胞计数。结论患有全身性狼疮红斑狼疮的威尼肽治疗与B淋巴细胞的暴露依赖性减少有关,以及较小程度,总淋巴细胞计数。该研究支持评估B细胞淋巴瘤-2抑制剂作为治疗系统性红斑狼疮的潜在疗法。 ClinicalTrials.gov NCT01686555。

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  • 来源
    《Clinical pharmacokinetics》 |2020年第3期|共13页
  • 作者单位

    AbbVie Inc Clin Pharmacol &

    Pharmacometr 1 North Waukegan Rd N Chicago IL 60064 USA;

    AbbVie Inc Clin Pharmacol &

    Pharmacometr 1 North Waukegan Rd N Chicago IL 60064 USA;

    AbbVie Inc Clin Pharmacol &

    Pharmacometr 1 North Waukegan Rd N Chicago IL 60064 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药理学;
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