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在健康受试者和ALK阳性非小细胞肺癌患者中评估色瑞替尼与质子泵抑制剂之间的药物相互作用潜力。

Assessment of drug-drug interaction potential between ceritinib and proton pump inhibitors in healthy subjects and in patients with ALK-positive non-small cell lung cancer.

作者信息

Lau Yvonne Y, Gu Wen, Lin Tiffany, Viraswami-Appanna Kalyanee, Cai Can, Scott Jeffrey W, Shi Michael

机构信息

Novartis Pharmaceuticals Corporation, One Health Plaza, East Hanover, NJ, 07936-1080, USA.

出版信息

Cancer Chemother Pharmacol. 2017 Jun;79(6):1119-1128. doi: 10.1007/s00280-017-3308-7. Epub 2017 Apr 19.

Abstract

PURPOSE

The impact of proton pump inhibitors (PPIs) on the pharmacokinetics (PK) and efficacy of ceritinib was evaluated.

METHODS

A healthy subject drug-drug interaction (DDI) study was conducted to assess the effect of esomeprazole on the PK of a single 750 mg dose of ceritinib. To further investigate the impact of PPIs on the PK and efficacy of ceritinib in ALK-positive cancer patients, two subgroup analyses were performed. Analysis 1 evaluated ceritinib steady-state trough concentration (C) and overall response rate (ORR) by concomitant use of PPIs in patients from the ASCEND-1, -2, and -3 studies; analysis 2 evaluated ceritinib single-dose and steady-state AUC and C by concomitant PPI use in patients from ASCEND-1 using a definition of PPI usage similar to that used in the healthy subject study.

RESULTS

In the healthy subject study, co-administration of a single 750 mg dose of ceritinib with esomeprazole 40 mg for 6 days decreased ceritinib AUC by 76% and C by 79%. However, based on subgroup analysis 1, patients had similar C and ORR regardless of concomitant PPI usage. Based on analysis 2, co-administration of a single 750 mg ceritinib dose with PPIs for 6 days in patients suggested less effect on ceritinib exposure than that observed in healthy subjects as AUC decreased by 30% and C decreased by 25%. No clinically meaningful effect on steady-state exposure was observed after daily dosing.

CONCLUSIONS

Long-term administration of ceritinib with PPIs does not adversely affect the PK and efficacy of ceritinib in ALK-positive cancer patients.

摘要

目的

评估质子泵抑制剂(PPI)对色瑞替尼药代动力学(PK)及疗效的影响。

方法

开展一项健康受试者药物相互作用(DDI)研究,以评估埃索美拉唑对单次750 mg剂量色瑞替尼PK的影响。为进一步研究PPI对ALK阳性癌症患者色瑞替尼PK及疗效的影响,进行了两项亚组分析。分析1评估了ASCEND-1、-2和-3研究中患者同时使用PPI时色瑞替尼的稳态谷浓度(C)及总缓解率(ORR);分析2使用与健康受试者研究中相似的PPI使用定义,评估了ASCEND-1研究中患者同时使用PPI时色瑞替尼的单剂量及稳态AUC和C。

结果

在健康受试者研究中,单次750 mg剂量的色瑞替尼与40 mg埃索美拉唑联合给药6天,使色瑞替尼的AUC降低了76%,C降低了79%。然而,根据亚组分析1,无论是否同时使用PPI,患者的C及ORR相似。根据分析2,在患者中单次750 mg色瑞替尼剂量与PPI联合给药6天,对色瑞替尼暴露的影响小于在健康受试者中观察到的情况,因为AUC降低了30%,C降低了25%。每日给药后,未观察到对稳态暴露有临床意义的影响。

结论

在ALK阳性癌症患者中,色瑞替尼与PPI长期联合给药不会对色瑞替尼的PK及疗效产生不利影响。

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