Therapeutic drug monitoring of osimertinib in non‐small cell lung cancer and short bowel syndrome: A case report

Author:

Longuespée Rémi12ORCID,Kunz Julia34,Fresnais Margaux1,Foerster Kathrin I.1,Burhenne Jürgen1,Thomas Michael35,Kazdal Daniel56,Stenzinger Albrecht56,Christopoulos Petros35,Haefeli Walter E.1ORCID

Affiliation:

1. Department of Clinical Pharmacology and Pharmacoepidemiology Heidelberg University Hospital Heidelberg Germany

2. Metabolic Crosstalk in Cancer German Cancer Research Center (DKFZ) Heidelberg Germany

3. Department of Thoracic Oncology Thoraxklinik at Heidelberg University Hospital and National Center for Tumor Diseases Heidelberg Germany

4. Medical Care Center for Oncology and Hematology GRN Sinsheim Germany

5. Translational Lung Research Center Heidelberg (TLRC‐H), member of the German Center for Lung Research (DZL) Heidelberg Germany

6. Institute of Pathology Heidelberg University Hospital Heidelberg Germany

Abstract

Short bowel syndrome (SBS) following extensive intestinal resection is often characterized by impaired absorption of orally administered drugs, including tyrosine kinase inhibitors (TKI). We report the case of a patient with EGFR‐mutated non‐small cell lung carcinoma treated with 80 mg/day of the TKI osimertinib who achieved partial response of the tumour, but was subsequently subjected to a double‐barrelled jejunostomy due to ileus. Due to the development of SBS after the bypass surgery, plasma concentrations of osimertinib were monitored using mass spectrometry. The therapeutic drug monitoring confirmed a malabsorption of osimertinib in the patient (108 ng/mL, which is below the 5th percentile of the expected plasma concentration) and was useful to guide adjustments of TKI dosing in order to achieve adequate blood levels (161 ng/mL after increase of the dose to 120 mg/day) in order to maintain tumour control.

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

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