Literature DB >> 28424965

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.

Yvonne Y Lau1, Wen Gu2, Tiffany Lin2, Kalyanee Viraswami-Appanna2, Can Cai2, Jeffrey W Scott2, Michael Shi2.   

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 (Ctrough,ss) 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 AUC0-24h and C max 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 AUC0-∞ by 76% and C max by 79%. However, based on subgroup analysis 1, patients had similar C trough,ss 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 AUC0-24h decreased by 30% and C max 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.

Entities:  

Keywords:  Anaplastic lymphoma kinase; Ceritinib; Drug–drug interactions; Esomeprazole; Proton pump inhibitors

Mesh:

Substances:

Year:  2017        PMID: 28424965     DOI: 10.1007/s00280-017-3308-7

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  6 in total

Review 1.  Clinical Pharmacokinetics of Anaplastic Lymphoma Kinase Inhibitors in Non-Small-Cell Lung Cancer.

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Review 2.  Applications, Challenges, and Outlook for PBPK Modeling and Simulation: A Regulatory, Industrial and Academic Perspective.

Authors:  Wen Lin; Yuan Chen; Jashvant D Unadkat; Xinyuan Zhang; Di Wu; Tycho Heimbach
Journal:  Pharm Res       Date:  2022-05-13       Impact factor: 4.580

3.  Effects of magnesium oxide on pharmacokinetics of L-dopa/carbidopa and assessment of pharmacodynamic changes by a model-based simulation.

Authors:  Yushi Kashihara; Yui Terao; Kensaku Yoda; Takeshi Hirota; Toshio Kubota; Miyuki Kimura; Shunji Matsuki; Masaaki Hirakawa; Shin Irie; Ichiro Ieiri
Journal:  Eur J Clin Pharmacol       Date:  2018-10-31       Impact factor: 2.953

4.  Ribociclib Bioavailability Is Not Affected by Gastric pH Changes or Food Intake: In Silico and Clinical Evaluations.

Authors:  Tanay S Samant; Shyeilla Dhuria; Yasong Lu; Marc Laisney; Shu Yang; Arnaud Grandeury; Martin Mueller-Zsigmondy; Kenichi Umehara; Felix Huth; Michelle Miller; Caroline Germa; Mohamed Elmeliegy
Journal:  Clin Pharmacol Ther       Date:  2017-12-08       Impact factor: 6.875

Review 5.  Pharmacokinetic-Based Drug-Drug Interactions with Anaplastic Lymphoma Kinase Inhibitors: A Review.

Authors:  Dehua Zhao; Jing Chen; Mingming Chu; Xiaoqing Long; Jisheng Wang
Journal:  Drug Des Devel Ther       Date:  2020-04-30       Impact factor: 4.162

Review 6.  Proton Pump Inhibitors and Cancer: Current State of Play.

Authors:  Marie Bridoux; Nicolas Simon; Anthony Turpin
Journal:  Front Pharmacol       Date:  2022-03-14       Impact factor: 5.810

  6 in total

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