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.

Oncology
|June 15, 2018
PubMed
Abstract

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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