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聚乙二醇化重组人粒细胞集落刺激因子给药后转移性乳腺癌患者中纳武紫杉醇的群体药代动力学和暴露-毒性分析。

Population pharmacokinetic and exposure-toxicity analyses of nab-paclitaxel after pegylated recombinant human granulocyte colony-stimulating factor administration in patients with metastatic breast cancer.

机构信息

Department of Pharmacy, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, 1 East Banshan Road, Hangzhou, Zhejiang, 310022, China.

Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery System, Department of Pharmaceutics, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China.

出版信息

Cancer Chemother Pharmacol. 2024 Oct;94(4):523-534. doi: 10.1007/s00280-024-04702-3. Epub 2024 Jul 31.

Abstract

PURPOSE

This study aimed to establish a population pharmacokinetic (PK) model to evaluate the dynamic relationship between the concentrations of total and unbound paclitaxel, and the exposure-response analysis of albumin-bound paclitaxel (nab-paclitaxel) after pegylated recombinant human granulocyte colony-stimulating factor (PEG-G-CSF) administration in patients with metastatic breast cancer.

METHODS

A total of 653 concentrations corresponding to total paclitaxel and 334 concentrations corresponding to unbound paclitaxel were analyzed in 24 subjects who randomized received a single 260 mg/m dose of two nab-paclitaxel formulations with a 21-35-day washout period. PEG-G-CSF was administered to all the patients in each cycle to prevent neutropenia. The exposure-response relationships were evaluated using the exposure to total, albumin-coated, and unbound paclitaxel, as well as the reduction in neutrophil count. The exposure data were analyzed using nonlinear mixed-effect modeling. A linear regression model was used to test the statistical significance of the correlation between percentage of reduction in neutrophil count and exposure.

RESULTS

The PK characteristics of total paclitaxel were described using a three-compartment model with first-order elimination, and a mechanism-based model incorporating linear release of nab-paclitaxel and the saturated binding of unbound paclitaxel to plasma components was established. The release ratio of paclitaxel from nab-paclitaxel was estimated to be 4.60% and the maximum unbound fraction (2.76%) was reached at the end of the infusion. The study found that a longer duration of total paclitaxel concentration > 0.19 µmol/L was significantly correlated with a reduction in neutrophil count (r = 0.23, P = 0.00062). Specifically, a duration of > 8.6 h was a predictor of a decreased neutrophil count.

CONCLUSION

The decrease in neutrophils induced by nab-paclitaxel was significantly correlated with the duration above a total paclitaxel concentration of 0.19 µmol/L despite the use of PEG-G-CSF.

摘要

目的

本研究旨在建立群体药代动力学(PK)模型,以评估聚乙二醇化重组人粒细胞集落刺激因子(PEG-G-CSF)给药后转移性乳腺癌患者总紫杉醇和游离紫杉醇浓度之间的动态关系,并进行白蛋白结合紫杉醇(nab-紫杉醇)的暴露-反应分析。

方法

对 24 名受试者进行了分析,这些受试者随机接受了两种 nab-紫杉醇制剂单次 260mg/m 剂量,洗脱期为 21-35 天。每个周期均给所有患者使用 PEG-G-CSF 以预防中性粒细胞减少症。使用总紫杉醇、白蛋白包裹紫杉醇和游离紫杉醇的暴露以及中性粒细胞计数减少来评估暴露-反应关系。使用非线性混合效应模型分析暴露数据。线性回归模型用于检验中性粒细胞计数减少百分比与暴露之间相关性的统计学意义。

结果

采用三房室模型和一级消除描述总紫杉醇的 PK 特征,并建立了一种包含 nab-紫杉醇线性释放和游离紫杉醇与血浆成分饱和结合的机制模型。从 nab-紫杉醇中释放的紫杉醇的释放比例估计为 4.60%,在输注结束时达到最大游离分数(2.76%)。研究发现,总紫杉醇浓度>0.19μmol/L 的持续时间与中性粒细胞计数减少呈显著相关(r=0.23,P=0.00062)。具体来说,持续时间>8.6 h 是中性粒细胞计数减少的预测因子。

结论

尽管使用了 PEG-G-CSF,但 nab-紫杉醇引起的中性粒细胞减少与总紫杉醇浓度>0.19μmol/L 以上的持续时间显著相关。

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