Blood Concentrations of Osimertinib and Its Active Metabolites: Impact on Treatment Efficacy and Safety.
By: Takae Okuno, Masafumi Hongoh, Ryosuke Tanino, Tamio Okimoto, Yukari Tsubata, Takeshi Isobe

Division of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Shimane University Faculty of Medicine, Shimane, Japan.
2025-3-11; doi: 10.21873/anticanres.17627
Abstract

Background/aim

Osimertinib (OSI) is a third-generation epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) and the standard treatment for non-small cell lung cancer with EGFR mutation. OSI contains active metabolites such as AZ5104 and AZ7550. The correlation between the blood concentrations of OSI, AZ5104, and AZ7550 with their efficacy and safety is not clear; hence, we examined it.

Patients

This was a single-center, retrospective study. We measured the blood concentrations of OSI, AZ5104, and AZ7550 in 46 patients who received OSI between March 2016 and December 2022 and examined their relationships with progression-free survival (PFS), overall survival (OS), and adverse events.

Results

The high OSI group had a longer PFS than the low OSI group (26.5 vs. 17.9 months, p=0.058); however, blood levels of AZ7550 and AZ5104 were not correlated with PFS. In the multivariate analysis, blood OSI concentration was an independent prognostic factor for PFS. Overall survival was not different between patients with high or low blood levels of OSI, AZ5104, or AZ7550. In terms of safety, AZ7550 blood levels were higher in patients with higher grades of neutropenia, lymphopenia and anemia, whereas AZ5104 blood levels were higher in patients with higher grades of lymphopenia.

Conclusion

Higher OSI blood concentrations were associated with a longer PFS, while higher blood concentrations of AZ5104 and AZ7550 were observed in patients with higher hematological toxicity grades. Further research is needed to determine the optimal blood levels of OSI that improve prognosis and minimize toxicity.



Copyright © 2025 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

PMID:40425344






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