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Epidermal growth factor receptor inhibitors: a review of cutaneous adverse events and management
K Chanprapaph1, V Vachiramon1, P Rattanakaemakorn1
1Division of Dermatology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Rajthevi, Bangkok 10400, Thailand.
Abstract:
Epidermal growth factor inhibitors (EGFRI), the first targeted cancer therapy, are currently an essential treatment for many advance-stage epithelial cancers. These agents have the superior ability to target cancers cells and better safety profile compared to conventional chemotherapies. However, cutaneous adverse events are common due to the interference of epidermal growth factor receptor (EGFR) signaling in the skin. Cutaneous toxicities lead to poor compliance, drug cessation, and psychosocial discomfort. This paper summarizes the current knowledge concerning the presentation and management of skin toxicity from EGFRI. The common dermatologic adverse events are papulopustules and xerosis. Less common findings are paronychia, regulatory abnormalities of hair growth, maculopapular rash, mucositis, and postinflammatory hyperpigmentation. Radiation enhances EGFRI rash due to synergistic toxicity. There is a positive correlation between the occurrence and severity of cutaneous adverse effects and tumor response. To date, prophylactic systemic tetracycline and tetracycline class antibiotics have proven to be the most effective treatment regime.
Insights
Epidermal growth factor inhibitors (EGFRI) treat epithelial cancers but cause skin toxicity. Prophylactic tetracycline antibiotics are the most effective management strategy for these common, yet manageable, adverse events.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Epidermal growth factor inhibitors (EGFRI) represent a significant advancement in targeted cancer therapy for advanced epithelial cancers.
- While offering improved efficacy and safety over traditional chemotherapy, EGFRI frequently cause cutaneous adverse events due to EGFR signaling interference in the skin.
Purpose of the Study:
- To summarize current knowledge on the presentation and management of skin toxicities associated with EGFRI therapy.
- To highlight the correlation between cutaneous adverse effects and therapeutic response.
Main Methods:
- Literature review summarizing clinical presentations of EGFRI-induced dermatologic toxicities.
- Analysis of treatment strategies, focusing on prophylactic and therapeutic interventions.
Main Results:
- Common skin toxicities include papulopustules and xerosis; less common are paronychia, hair growth abnormalities, maculopapular rash, mucositis, and postinflammatory hyperpigmentation.
- Radiation therapy can potentiate EGFRI-induced rashes.
- A positive correlation exists between the severity of skin toxicity and tumor response.
Conclusions:
- Cutaneous adverse events from EGFRI significantly impact patient compliance and quality of life.
- Prophylactic administration of tetracycline or tetracycline-class antibiotics is the most effective current management strategy for EGFRI-related skin toxicity.
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