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.

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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