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多西他赛及其三种主要代谢产物在蒽环类药物治疗难治的晚期乳腺癌患者中的药代动力学:一项欧洲癌症中心(ECC)试验(多西他赛采用3小时输注)

Pharmacokinetics of paclitaxel and three major metabolites in patients with advanced breast carcinoma refractory to anthracycline therapy treated with a 3-hour paclitaxel infusion: a European Cancer Centre (ECC) trial.

作者信息

Huizing M T, Vermorken J B, Rosing H, ten Bokkel Huinink W W, Mandjes I, Pinedo H M, Beijnen J H

机构信息

Department of Medical Oncology, Free University Hospital, Amsterdam, The Netherlands.

出版信息

Ann Oncol. 1995 Sep;6(7):699-704. doi: 10.1093/oxfordjournals.annonc.a059287.

Abstract

BACKGROUND

Hepatic metabolism and biliary clearance play pivotal roles in the disposition of the anticancer drug paclitaxel. 6-alpha-hydroxypaclitaxel, 3'-p-hydroxypaclitaxel and 6-alpha,3'-p-dihydroxypaclitaxel were the major metabolic products of paclitaxel found in human bile. Recently, these metabolic products were detected in human plasma. The pharmacokinetics of paclitaxel and its metabolites were investigated in anthracycline-resistant breast cancer patients treated with high-dose paclitaxel and granulocyte colony-stimulating factor (G-CSF) support.

PATIENTS AND METHODS

Nine patients were entered into this study in which paclitaxel was administered at the relatively high dose of 250 mg/m2 during a 3-hour infusion. G-CSF was administered daily subcutaneously (s.c.)on days 2 to 19 following chemotherapy. Analysis of paclitaxel and metabolite concentrations was performed by a new highly sensitive reversed-phase high performance liquid chromatographic (HPLC) assay.

RESULTS

The dose-limiting toxicity in this study was cumulative neurotoxicity. One patient had a partial response and 2 patients had mixed responses of their skin metastases. Relatively low peak plasma concentration (Cmax), with mean values of 6.91 micromol/L (range 3.08 to 8.98) and area under the plasma concentration time curve (AUC), with mean values of 27.04 micromol/L.h (range 14.88 to 40.57), were observed. The total body clearance was 16.99 L/h (range, 10.25 to 27.39). The pharmacokinetic parameter for the prediction of leuko-neutropenia, the duration of the plasma concentration above the threshold of 0.1 micromol/L.h (T > or = 0.1 microM), was 19.72 h (range 10.54 to 26.31). The three major metabolites detected in human plasma were identified as 6-alpha-hydroxypaclitaxel, 3'-p-hydroxypaclitaxel and 6-alpha,3'-p-dihydroxypaclitaxel. Cmax and AUC values of these metabolites are reported.

CONCLUSIONS

The three main metabolic products of paclitaxel in human plasma are 6-alpha-hydroxypaclitaxel, 3'-p-hydroxypaclitaxel and the dihydroxymetabolite 6-alpha,3'-p-dihydroxypaclitaxel. Two patients with liver function disturbances showed a tendency to higher paclitaxel and 6-alpha-hydroxypaclitaxel AUC levels, with more pronounced neuropathy.

摘要

背景

肝脏代谢和胆汁清除在抗癌药物紫杉醇的处置过程中起着关键作用。6-α-羟基紫杉醇、3'-对羟基紫杉醇和6-α,3'-对二羟基紫杉醇是在人胆汁中发现的紫杉醇主要代谢产物。最近,这些代谢产物在人血浆中被检测到。在接受高剂量紫杉醇和粒细胞集落刺激因子(G-CSF)支持治疗的蒽环类耐药乳腺癌患者中,对紫杉醇及其代谢产物的药代动力学进行了研究。

患者与方法

9名患者进入本研究,在3小时输注期间以相对高剂量250mg/m²给予紫杉醇。化疗后第2至19天每天皮下注射G-CSF。通过一种新的高灵敏度反相高效液相色谱(HPLC)分析法对紫杉醇和代谢产物浓度进行分析。

结果

本研究中的剂量限制性毒性为累积性神经毒性。1例患者部分缓解,2例患者皮肤转移灶有混合反应。观察到相对较低的血浆峰浓度(Cmax),平均值为6.91μmol/L(范围3.08至8.98),以及血浆浓度时间曲线下面积(AUC),平均值为27.04μmol/L·h(范围14.88至40.57)。全身清除率为16.99L/h(范围10.25至27.39)。预测白细胞减少症的药代动力学参数,即血浆浓度高于0.1μmol/L·h阈值的持续时间(T≥0.1μM)为19.72h(范围10.54至26.31)。在人血浆中检测到的三种主要代谢产物被鉴定为6-α-羟基紫杉醇、3'-对羟基紫杉醇和6-α,3'-对二羟基紫杉醇。报告了这些代谢产物的Cmax和AUC值。

结论

人血浆中紫杉醇的三种主要代谢产物为6-α-羟基紫杉醇、3'-对羟基紫杉醇和二羟基代谢产物6-α,3'-对二羟基紫杉醇。两名肝功能障碍患者显示紫杉醇和6-α-羟基紫杉醇AUC水平有升高趋势,神经病变更明显。

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