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表皮生长因子受体突变的非小细胞肺癌患者中,增加剂量厄洛替尼治疗中枢神经系统转移的疗效。

Efficacy of increased-dose erlotinib for central nervous system metastases in non-small cell lung cancer patients with epidermal growth factor receptor mutation.

机构信息

Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawaracho, Sakyo-ku, Kyoto, 606-8507, Japan.

出版信息

Cancer Chemother Pharmacol. 2011 Oct;68(4):1089-92. doi: 10.1007/s00280-011-1691-z. Epub 2011 Jun 17.

Abstract

PURPOSE

Recent reports indicate that refractory central nervous system (CNS) metastases of non-small cell lung cancer (NSCLC) are improved by high-dose gefitinib or erlotinib administration. We describe a Japanese woman with NSCLC and CNS metastases who was resistant to 75 mg daily erlotinib, but the metastases were improved by 150 mg daily erlotinib. We investigated the plasma and CSF concentrations of erlotinib at each dose as well as the correlation between the plasma and CSF concentrations of erlotinib.

METHODS

Including this patient, we administered 150 mg erlotinib daily to nine NSCLC patients with CNS metastases and measured the plasma and CSF concentrations just before administration on day 8. The concentrations were determined using high-performance liquid chromatography with ultraviolet detection.

RESULTS

The plasma and CSF concentrations of erlotinib at a dose of 75 mg were 433 and 14 nM, respectively. The plasma and CSF concentrations of erlotinib at a dose of 150 mg were increased to 1,117 and 44 nM, respectively. The mean ± standard deviation of CSF concentrations and penetration rates were 106 ± 59 nM and 4.5 ± 1.5%, respectively. There was a good correlation (R(2) = 0.84) between plasma and CSF concentrations (P = 0.0005).

CONCLUSIONS

This study indicates that CSF concentrations of erlotinib depend on its plasma concentration. As seen in this patient, high CSF concentrations of erlotinib can be achieved by high-dose administration, and this finding suggests the efficacy of high-dose administration, especially to refractory CNS metastases of NSCLC patients.

摘要

目的

最近的报告表明,大剂量吉非替尼或厄洛替尼给药可改善难治性非小细胞肺癌(NSCLC)中枢神经系统(CNS)转移。我们描述了一例 NSCLC 伴 CNS 转移的日本女性患者,该患者对每天 75mg 厄洛替尼耐药,但每天 150mg 厄洛替尼可改善转移。我们研究了每个剂量的厄洛替尼的血浆和 CSF 浓度以及厄洛替尼的血浆和 CSF 浓度之间的相关性。

方法

包括该患者在内,我们每天给 9 例 NSCLC 伴 CNS 转移的患者服用 150mg 厄洛替尼,并在第 8 天给药前测定血浆和 CSF 浓度。浓度使用高效液相色谱法结合紫外检测法测定。

结果

厄洛替尼剂量为 75mg 时,血浆和 CSF 浓度分别为 433 和 14nM。厄洛替尼剂量为 150mg 时,血浆和 CSF 浓度分别增加至 1117 和 44nM。CSF 浓度和穿透率的平均值±标准偏差分别为 106±59nM 和 4.5±1.5%。血浆和 CSF 浓度之间存在良好的相关性(R(2)=0.84)(P=0.0005)。

结论

本研究表明,厄洛替尼的 CSF 浓度取决于其血浆浓度。如该患者所见,通过高剂量给药可获得较高的 CSF 厄洛替尼浓度,这一发现提示高剂量给药的疗效,特别是对 NSCLC 患者难治性 CNS 转移的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f203/3180562/fa1fa86f4f05/280_2011_1691_Fig1_HTML.jpg

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