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Drug eruptions with novel targeted therapies - immune checkpoint and EGFR inhibitors
Isabella Pospischil1, Wolfram Hoetzenecker1
1Department of Dermatology, Kepler University Hospital, Johannes Kepler University, Linz, Austria.
Abstract:
Given the increasing use of novel targeted therapies, dermatologists are constantly confronted with novel cutaneous side effects of these agents. A rapid diagnosis and appropriate management of these side effects are crucial to prevent impairment of the patients' quality of life and interruptions of essential cancer treatments. Immune checkpoint and EGFR inhibitors are frequently used targeted therapies for various malignancies and are associated with a distinct spectrum of cutaneous adverse events. Exanthematous drug eruptions represent a particular diagnostic challenge in these patients. Immune checkpoint inhibitors can elicit a plethora of immune-related exanthemas, most commonly maculopapular, lichenoid, and psoriasiform eruptions. Additionally, autoimmune bullous dermatoses and exanthemas associated with connective tissue diseases may arise. In cases of severe, atypical or therapy-resistant presentations an extensive dermatological investigation including a skin biopsy is recommended. Topical and systemic steroids are the mainstay of treatment. Papulopustular eruptions represent the major cutaneous adverse effect of EGFR inhibitor therapy, occurring in up to 90 % of patients within the first two weeks of therapy, depending on the agent. Besides topical antibiotics and steroids, oral tetracyclines are the first choice in systemic treatment and can also be used as prophylaxis.
Insights
Novel targeted cancer therapies, like immune checkpoint inhibitors and EGFR inhibitors, cause unique skin side effects. Prompt diagnosis and management of these cutaneous adverse events are vital for patient care and treatment continuity.
Area of Science:
- Dermatology
- Oncology
- Pharmacology
Background:
- Novel targeted therapies, including immune checkpoint inhibitors and epidermal growth factor receptor (EGFR) inhibitors, are increasingly used for cancer treatment.
- These therapies are associated with a distinct spectrum of cutaneous adverse events that pose diagnostic and management challenges for dermatologists.
- Understanding these side effects is crucial for maintaining patient quality of life and preventing interruptions in cancer therapy.
Purpose of the Study:
- To review the spectrum of cutaneous adverse events associated with immune checkpoint inhibitors and EGFR inhibitors.
- To highlight diagnostic challenges, particularly for exanthematous drug eruptions.
- To outline current management strategies for these therapy-related skin toxicities.
Main Methods:
- Literature review of cutaneous side effects associated with immune checkpoint inhibitors and EGFR inhibitors.
- Discussion of diagnostic approaches, including skin biopsy for severe or atypical cases.
- Overview of treatment modalities, including topical and systemic corticosteroids, antibiotics, and tetracyclines.
Main Results:
- Immune checkpoint inhibitors can cause various immune-related exanthemas, such as maculopapular, lichenoid, and psoriasiform eruptions, and may unmask autoimmune conditions.
- EGFR inhibitors frequently cause papulopustular eruptions, affecting up to 90% of patients early in treatment.
- Topical/systemic steroids are primary treatments for immune-related eruptions, while topical antibiotics, steroids, and oral tetracyclines are key for EGFR inhibitor-induced papulopustular eruptions.
Conclusions:
- Dermatologists must be adept at recognizing and managing novel cutaneous side effects from targeted cancer therapies.
- Early and accurate diagnosis, alongside appropriate management, is essential to mitigate patient morbidity and treatment disruption.
- Specific treatment protocols exist for different classes of targeted therapy-induced skin toxicities, emphasizing corticosteroids and tetracyclines.
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