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Published on: May 20, 2020
Semiology of skin toxicity associated with epidermal growth factor receptor (EGFR) inhibitors
L Peuvrel1, C Bachmeyer, Z Reguiai
1Department of Dermato-Cancerology, Nantes University Hospital; CIC biotherapy INSERM 0305, 1 place Ricordeau, 44000, Nantes, France.
Purpose:
Advances in the understanding of the mechanisms involved in oncogenesis have led to the development of so-called targeted therapies such as epidermal growth factor receptor (EGFR) inhibitors, which take on an increasingly important role in the management of cancer. These treatments have the advantage not to trigger the adverse effects traditionally encountered with chemotherapy, such as nausea, vomiting or haematological toxicity. However, they do cause new forms of toxicity: the most common one is skin toxicity. It is important to be aware of it because it can be debilitating, adversely impacting patients' quality of life and altering treatment compliance, although it appears to be correlated with treatment response in certain series. Non-specialists can have difficulty in recognising this unusual skin toxicity.
Methods:
The dermatologic side effects most frequently triggered by EGFR inhibitors are discussed in this article.
Results:
They are divided into three categories depending on their target: inflammation of the pilo-sebaceous follicle, represented by EGFR inhibitor-associated folliculitis, which occurs at an early stage and is frequent; alteration in the skin barrier, primarily responsible for xerosis, fissures and pruritus, which are frequent and delayed; and lesions of the skin appendages (paronychia, pyogenic granuloma, hair changes), which are delayed and less frequent.
Conclusion:
It is essential for all practitioners concerned to know about these dermatologic side effects in order to ensure better global management of patients, particularly in terms of quality of life.
Insights
Epidermal growth factor receptor (EGFR) inhibitors cause unique skin toxicities, including folliculitis, skin barrier changes, and appendage lesions. Early recognition and management are crucial for patient quality of life and treatment adherence.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Targeted cancer therapies, such as epidermal growth factor receptor (EGFR) inhibitors, are increasingly used in cancer management.
- Unlike traditional chemotherapy, EGFR inhibitors offer advantages like reduced nausea and hematological toxicity.
- However, these targeted therapies commonly induce distinct dermatologic side effects, impacting patient quality of life and treatment compliance.
Purpose of the Study:
- To discuss the dermatologic side effects associated with epidermal growth factor receptor (EGFR) inhibitors.
- To raise awareness among healthcare professionals regarding these specific toxicities.
- To emphasize the importance of recognizing and managing these side effects for optimal patient care.
Main Methods:
- Review of dermatologic side effects triggered by EGFR inhibitors.
- Categorization of side effects based on their affected target.
- Discussion of the timing and frequency of each side effect category.
Main Results:
- EGFR inhibitor-associated folliculitis: an early-stage, frequent inflammatory condition targeting the pilo-sebaceous follicle.
- Alterations in the skin barrier: leading to xerosis, fissures, and pruritus, typically occurring later and frequently.
- Lesions of skin appendages: including paronychia, pyogenic granuloma, and hair changes, which are less frequent and appear later.
Conclusions:
- Dermatologic side effects from EGFR inhibitors are common and can be debilitating.
- Awareness and recognition of these toxicities are essential for effective patient management.
- Proper management of skin toxicity improves patient quality of life and treatment adherence, potentially correlating with treatment response.
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