Influence of Food With Different Fat Concentrations on Alectinib Exposure: A Randomized Crossover Pharmacokinetic Trial

Author:

Lanser Daan A.C.1,de Leeuw Simon P.12,Oomen-de Hoop Esther1,de Bruijn Peter1,Paats Marthe S.2,Dumoulin Daphne W.2,Koolen Stijn L.W.13,Dingemans Anne-Marie C.2,Mathijssen Ron H.J.1,Veerman G.D. Marijn1

Affiliation:

1. Department of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, the Netherlands

2. Department of Pulmonology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, the Netherlands

3. Department of Pharmacy and Pharmacology, Erasmus University Medical Center, Rotterdam, the Netherlands

Abstract

Background: Alectinib is the keystone treatment in advanced anaplastic lymphoma kinase–positive (ALK+) non–small cell lung cancer (NSCLC). An exposure–response threshold of 435 ng/mL has recently been established, albeit 37% of patients do not reach this threshold. Alectinib is orally administered, and absorption is largely influenced by food. Hence, further investigation into this relationship is needed to optimize its bioavailability. Patients and Methods: In this randomized 3-period crossover clinical study in ALK+ NSCLC, alectinib exposure was compared among patients with different diets. Every 7 days, the first alectinib dose was taken with either a continental breakfast, 250-g of low-fat yogurt, or a self-chosen lunch, and the second dose was taken with a self-chosen dinner. Sampling for alectinib exposure (Ctrough) was performed at day 8, just prior to alectinib intake, and the relative difference in Ctrough was compared. Results: In 20 evaluable patients, the mean Ctrough was 14% (95% CI, −23% to −5%; P=.009) and 20% (95% CI, −25% to −14%; P<.001) lower when taken with low-fat yogurt compared with a continental breakfast and a self-chosen lunch, respectively. Administration with a self-chosen lunch did not change exposure compared with a continental breakfast (+7%; 95% CI, −2% to +17%; P=.243). In the low-fat yogurt period, 35% of patients did not reach the threshold versus 5% with the other meals (P<.01). Conclusions: Patients and physicians should be warned for a detrimental food–drug interaction when alectinib is taken with low-fat yogurt, because it results in a clinically relevant lower alectinib exposure. Intake with a self-chosen lunch did not change drug exposure and could be a safe and patient-friendly alternative.

Publisher

Harborside Press, LLC

Subject

Oncology

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