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Updated: Feb 9, 2026

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Relationship between Paronychia and Drug Concentrations of Epidermal Growth Factor Receptor Tyrosine Kinase
Katsuhiro Masago1,2, Kei Irie3, Shiro Fujita1,2
1Department of Pathology and Molecular Diagnostics, Aichi Cancer Center, Nagoya, Japan.
Purpose:
The purpose of the study was to evaluate the site of paronychia in patients with non-small cell lung cancer harboring an epidermal growth factor receptor (EGFR) gene activating mutation who were treated with EGFR tyrosine kinase inhibitors (EGFR TKIs).
Patients And Methods:
The study included 55 patients with non-small-cell lung cancer who were treated with an EGFR TKIs. Resulting all toxicities were graded using the Common Terminology Criteria for Adverse Events version 4.0 system. Drug concentrations were determined with use of a quantum triple-quadrupole mass spectrometer and dried blood spots testing.
Results:
Paronychia most commonly occurred in the thumb and the big toe. There was no correlation between the severity of paronychia and the drug concentration of each EGFR TKI at the site of paronychia. The mean penetration rates of the drug from plasma to the tip of the finger and toe were 74.1% (erlotinib), 82.2% (gefitinib), and 99.9% (afatinib).
Conclusions:
High concentrations of an EGFR TKI at the affected site did not play a role in the onset mechanism of paronychia. Therefore, educating patients about ways to avoid compression may be a better approach to managing this adverse event than reducing the dose of the EGFR-TKI or stopping treatment.
Insights
Paronychia, a side effect of epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKIs), commonly affects thumbs and toes. High drug concentrations at the site do not cause paronychia, suggesting compression avoidance is key for management.
Area of Science:
- Oncology
- Pharmacology
- Dermatology
Background:
- Non-small cell lung cancer (NSCLC) treatment often involves epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKIs).
- Paronychia is a common adverse event associated with EGFR TKI therapy.
- Understanding the mechanism of EGFR TKI-induced paronychia is crucial for effective management.
Purpose of the Study:
- To investigate the specific sites of paronychia occurrence in NSCLC patients treated with EGFR TKIs.
- To evaluate the relationship between EGFR TKI drug concentrations at affected sites and paronychia severity.
- To determine the drug penetration rates into finger and toe tissues.
Main Methods:
- Retrospective analysis of 55 NSCLC patients receiving EGFR TKIs.
- Grading of toxicities using Common Terminology Criteria for Adverse Events (CTCAE) v4.0.
- Quantification of drug concentrations in dried blood spots using mass spectrometry.
Main Results:
- Paronychia most frequently developed in the thumb and big toe.
- No significant correlation was observed between paronychia severity and EGFR TKI drug concentration at the affected site.
- Mean drug penetration rates from plasma to extremities were 74.1% (erlotinib), 82.2% (gefitinib), and 99.9% (afatinib).
Conclusions:
- Elevated EGFR TKI concentrations at the site of paronychia do not appear to be the primary cause.
- Patient education on avoiding local compression may be more effective than dose reduction or treatment cessation for managing paronychia.
- Further research into preventative strategies beyond drug modification is warranted.
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