Treatment of epidermal growth factor receptor inhibitor-induced acneiform eruption with topical recombinant human

J U Shin1, J H Park, B-C Cho

  • 1Department of Dermatology, Severance Hospital, Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Korea.

Dermatology (Basel, Switzerland)
|September 26, 2012
PubMed
Abstract

Insights

Topical recombinant human EGF (rhEGF) effectively treated acneiform eruptions caused by epidermal growth factor receptor (EGFR) inhibitors. This approach may offer a new therapeutic option for managing this common side effect in cancer patients.

Area of Science:

  • Oncology
  • Dermatology
  • Molecular Biology

Background:

  • Epidermal growth factor receptor (EGFR) inhibitors are vital anticancer agents for solid tumors.
  • Skin toxicities, particularly acneiform eruptions, are common adverse effects of EGFR inhibitors.
  • Current treatments for EGFR inhibitor-induced acneiform eruptions yield varied responses.

Observation:

  • EGFR inhibitor treatment increased EGFR expression in HaCaT cells in a dose-dependent manner.
  • Newly synthesized EGFR may mediate biological actions in keratinocytes despite inhibitor presence.
  • Acneiform eruptions result from disturbed keratinocyte and hair follicle biology.

Findings:

  • Three patients with EGFR inhibitor-induced acneiform eruption showed positive responses to topical recombinant human EGF (rhEGF).
  • Topical rhEGF application was investigated as a treatment for EGFR inhibitor-induced acneiform eruption.
  • EGFR expression was evaluated in HaCaT cells post-EGFR inhibitor treatment.

Implications:

  • Topical rhEGF presents a potential therapeutic strategy for managing EGFR inhibitor-induced acneiform eruptions.
  • Restoring the EGF pathway locally may benefit patients experiencing this specific side effect.
  • Further research into rhEGF for managing EGFR inhibitor-related dermatologic toxicities is warranted.

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